Post on 09-Jan-2020
Alkaloid
Alkaloids are a group of naturally occurring chemical compounds that mostly contain basic nitrogen atoms, produced by a largevariety of organisms including bacteria, fungi, plants, and animals. This group also includes some related compounds with neutraland even weakly acidic properties. Compounds like amino acid peptides, proteins, nucleotides, nucleic acid, amines, and antibioticsare usually not called alkaloids. Alkaloids have a wide range of pharmacological activities including antimalarial, antiasthma,anticancer, cholinomimetic, vasodilatory, antiarrhythmic, analgesic, antibacterial, and antihyperglycemic activities. Many have founduse in traditional or modern medicine, or as starting points for drug discovery. Other alkaloids possess psychotropic and stimulantactivities, and have been used in entheogenic rituals or as recreational drugs. Alkaloids can be toxic too. Although alkaloids act on adiversity of metabolic systems in humans and other animals, they almost uniformly evoke a bitter taste.
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Alkaloid Inhibitors & Modulators
(+)-Bicuculline (d-Bicuculline) Cat. No.: HY-N0219
(+)-Bicuculline is a light-sensitive competitiveantagonist of .GABA-A receptor
Purity: 99.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg, 250 mg
(+)-Magnoflorine (Magnoflorine; α-Magnoflorine; Thalictrine) Cat. No.: HY-N0334
(+)-Magnoflorine (Magnoflorine) is an aporphinealkaloid found in , withAcoruscalamusanti-fungal activity, reduces the formation of C.
’ biofilm. Anti-antidiabetic andalbicansanti-oxidative activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(+)-SparteineCat. No.: HY-W008350
(+)-Sparteine is a natural alkaloid acting as aganglionic blocking agent. (+)-Sparteinecompetitively blocks in thenicotinic ACh receptorneurons.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
(+)-ViroallosecurinineCat. No.: HY-N5002
(+)-Viroallosecurinine, isolated from Securinega as a cytotoxic alkaloid, exhibits a MIC ofvirosa
0.48 μg/mL for and .Ps. Aeruginosa Staph. aureusAntibacterial activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
(-)-Cephaeline dihydrochloride (NSC 32944) Cat. No.: HY-N2260
(-)-Cephaeline dihydrochloride is an enantiomer ofCephaeline dihydrochloride. Cephaelinedihydrochloride is a selective inhibtorCYP2D6with of 121 μM.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 2 mg, 5 mg
(-)-CorynoxidineCat. No.: HY-N7010
(-)-Corynoxidine is an acetylcholinesteraseinhibitor with an value of 89.0 μM, isolatedIC50
from the aerial parts of .Corydalis speciosa(-)-Corynoxidine exhibits antibacterial activitiesagainst Staphylococcus aureus andmethicillin-resistant S.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(-)-Huperzine A (Huperzine A) Cat. No.: HY-17387
(-)-Huperzine A (Huperzine A), an activeLycopodium alkaloid extracted from traditionalChinese herb, is a potent, selective andreversible acetylcholinesterase (AChE) inhibitorand has been widely used in China for thetreatment of Alzheimer's disease (AD).
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg
(-)-Isocorypalmine (Tetrahydrocolumbamine; (S)-Tetrahydrocolumbamine) Cat. No.: HY-N0927
(-)-Isocorypalmine, an alkaloid isolated from, possesses antifungalCorydalis chaerophylla
activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
(-)-SecurinineCat. No.: HY-N2079
(-)-Securinine is plant-derived alkaloid and alsoa antagonist.GABA receptorA
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg
(-)-Sparteine ((-)-Lupinidine) Cat. No.: HY-W012185
(-)-Sparteine is a natural alkaloid isolated frombeans.
Purity: >98.0%Clinical Data: No Development ReportedSize: 100 mg
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(-)-Sparteine sulfate pentahydrate ((-)-Lupinidine (sulfate pentahydrate)) Cat. No.: HY-B1304
(-)-Sparteine sulfate pentahydrate ((-)-Lupinidinesulfate pentahydrate) is a class 1a antiarrhythmicagent and a sodium channel blocker. It is analkaloid, can chelate the bivalents calcium andmagnesium.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg
(-)-SalutaridineCat. No.: HY-N2256
(-)-Salutaridine (Salutaridine) is an alkaloidisolated from the stems of Sinomenium
.acutum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(R)-Fangchinoline (Thalrugosine; Thaligine) Cat. No.: HY-N1372
(R)-Fangchinoline (Thalrugosine), a alkaloids fromgenus exhibits antimicrobial andStephaniahypotensive activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(S)-NornicotineCat. No.: HY-W040430
(S)-Nornicotine is a metabolite of nicotine.
Purity: >98%Clinical Data:Size: 5 mg
(±)-10-Hydroxycamptothecin ((±)-10-HCPT) Cat. No.: HY-N0275
(±)-10-Hydroxycamptothecin, an indole alkaloidisolated from Camptotheca acuminate, inhibits theactivity of and has a broadtopoisomerase Ispectrum of anticancer activity.
Purity: >98%Clinical Data: No Development ReportedSize: 25 mg, 50 mg, 100 mg
(±)-Huperzine ACat. No.: HY-17388
(±)-Huperzine A, an active Lycopodium alkaloidextracted from traditional Chinese herb, is apotent, selective and reversibleacetylcholinesterase (AChE) inhibitor and has beenwidely used in China for the treatment ofAlzheimer's disease (AD).
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
1-Deoxynojirimycin (Duvoglustat) Cat. No.: HY-14860
1-Deoxynojirimycin (DNJ, Duvoglustat) is a potentα-glucosidase inhibitor, suppresses postprandialblood glucose, thereby possibly preventingdiabetes mellitus.
Purity: >98.0%Clinical Data: Phase 2Size: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
10-Deacetyl-7-xylosyl paclitaxel (10-Deacetyl-7-xylosyltaxol;
10-Deacetylpaclitaxel 7-Xyloside; …) Cat. No.: HY-20584
10-Deacetyl-7-xylosyl paclitaxel is a Paclitaxelderivative with improved pharmacological featuresand higher water solubility.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg, 50 mg
10-MethoxycamptothecinCat. No.: HY-N0446
10-Methoxycamptothecin is a natural bioactivederivative of camptothecin (CPT) isolated from
, and has beenCamptotheca acuminataconfirmed to possess high anti-cancer properties.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
12-EpinapellineCat. No.: HY-N2162
12-Epinapelline is a diterpene alkaloid isolatedfrom . 12-EpinapellineAconitum baikalenseexhibits Anti-inflammatory activity and stimulatesthe growth of colonies from fibroblast precursors.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
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2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) Cat. No.: HY-101412
2-(Methylamino)-1H-purin-6(7H)-one(N2-Methylguanine) is a modified nucleoside.2-(Methylamino)-1H-purin-6(7H)-one is anendogenous methylated nucleoside found in humanfluids.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 50 mg, 100 mg
2-Benzoxazolinone (2-Benzoxazolone; 1,3-Benzoxazol-2(3H)-one;
2-Hydroxybenzoxazole) Cat. No.: HY-W015818
2-Benzoxazolinone is an agentanti-leishmanialwith an of 40 μg/mL against . ALC50 L. donovanibuilding block in chemical synthesis.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
3-DeoxyaconitineCat. No.: HY-N2164
3-Deoxyaconitine is a diterpenoid alkaloid,isolated from Debx.Aconitum Carmichaeli
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
3-Hydroxypicolinic acid (Picolinic acid, 3-hydroxy-
(6CI,7CI,8CI); 2-Carboxy-3-hydroxypyridine) Cat. No.: HY-Y0030
3-Hydroxypicolinic acid is a picolinic acidderivative, and belongs to the pyridine family.
Purity: >97.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 g
3-Indoleacetic acid (Indole-3-acetic acid; 3-IAA) Cat. No.: HY-18569
3-Indoleacetic acid (Indole-3-acetic acid) is themost common natural plant growth hormone of theauxin class. It can be added to cell culturemedium to induce plant cell elongation anddivision.
Purity: 99.74%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 g
3-Indolepropionic acidCat. No.: HY-W015229
3-Indolepropionic acid is shown to be a powerfulantioxidant and has potential in the treatment forAlzheimer’s disease.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 g
3-Methyladenine (3-MA) Cat. No.: HY-19312
3-Methyladenine is a inhibitor.PI3K3-Methyladenine is a widely used inhibitor of
via its inhibitory effect on class IIIautophagyPI3K.
Purity: 99.84%Clinical Data: No Development ReportedSize: 50 mg, 100 mg, 200 mg, 500 mg
3-MethylxanthineCat. No.: HY-50723
3-Methylxanthine, a xanthine derivative, is acyclic guanosine monophosphate inhibitor,(GMP)with an of 920 μM on guinea-pig isolatedIC50
trachealis muscle.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
5,6-Dihydro-5-methyluracil (Dihydrothymine) Cat. No.: HY-N6787
5,6-Dihydro-5-methyluracil (Dihydrothymine), anintermediate breakdown product of thymine, comesfrom animal or plants. 5,6-Dihydro-5-methyluracil(Dihydrothymine) can be toxic when present atabnormally high levels.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
5-MethyluridineCat. No.: HY-W009444
5-Methyluridine is a is an endogenous methylatednucleoside found in human fluids.
Purity: 98.82%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 g
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6-Biopterin (L-Biopterin) Cat. No.: HY-102015
6-Biopterin (L-Biopterin), a pterin derivative, isa cofactor.NO synthase
Purity: 98.02%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
6-Chloropurine (6-Chloro-9H-purine) Cat. No.: HY-Y0247
6-Chloropurine is a building block in chemicalsynthesis. Intermediate in the preparation of9-alkylpurines and 6-rnercaptopurine. Antitumoractivities.
Purity: >97.0%Clinical Data: No Development ReportedSize: 100 mg
6-Methoxy DihydrosanguinarineCat. No.: HY-N4228
6-Methoxy Dihydrosanguinarine is an lkaloidisolated from the fruits of M.cordata. 6-MethoxyDihydrosanguinarine shows strong cytotoxicityagainst MCF-7 and SF-268 cell lines with IC50
values of 0.61 μM and 0.54 μM, respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
7-EthylcamptothecinCat. No.: HY-N2108
7-Ethylcamptothecin is one of camptothecinanalogues. camptothecin (CPT), a cytotoxicalkaloid isolated from Camptotheca
, is shown to have strong antitumoracuminateactivity against L1210 leukemia and Walker 256carcinosarcoma models.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
7-MethylxanthineCat. No.: HY-W017163
7-Methylxanthine, a methyl derivative of xanthine,is one of the purine components in urinarycalculi.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg
9-MethoxycamptothecinCat. No.: HY-N6011
9-Methoxycamptothecin (MCPT), isolated from, has antitumor activitiesNothapodytes foetida
through inhibition.topoisomerase9-Methoxycamptothecin (MCPT) induces strong G2/Marrest and in cancer.apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
AaptamineCat. No.: HY-N4225
Aaptamine, a spongean alkaloid isolated from a seasponge Aaptos aaptos, is a competitive antagonistof and activates the p21 promoterα-adrenoceptorin a p53-independent manner.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Acetylcholine chloride (Ach; ACh chloride) Cat. No.: HY-B0282
Acetylcholine (chloride) is a common found in the central andneurotransmitter
peripheral nerve system.
Purity: >99.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 g, 5 g
AcetylcorynolineCat. No.: HY-N0759
Acetylcorynoline is the major alkaloid componentderived from , and hasCorydalis bungeanaanti-inflammatory properties.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Acetylseneciphylline N-oxideCat. No.: HY-N6848
Acetylseneciphylline N-oxide is a pyrrolizinealkaloid that is seneciphylline in which thehydroxy hydrogen is replaced by an acetyl groupand the tertiary amino function is oxidised to thecorresponding N-oxide.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
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Acipimox (K-9321) Cat. No.: HY-B0283
Acipimox is a niacin derivative used as ahypolipidemic agent. Target: Acipimox is a niacinderivative used as a hypolipidemic agent.
Purity: >99.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
AcoforestinineCat. No.: HY-N4163
Acoforestinine is a diterpenoid alkaloid isolatedfrom .Aconitum handelianum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Aconine (Jesaconine) Cat. No.: HY-N0277
Aconine inhibits receptor activator of nuclearfactor (NF)-κB ligand (RANKL)-induced NF-κBactivation.
Purity: 99.23%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Adenine (6-Aminopurine; Vitamin B4) Cat. No.: HY-B0152
Adenine is a purine derivative and a nucleobasewith a variety of roles in biochemistry.
Purity: 98.76%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 g, 5 g
Adenine hemisulfate (6-Aminopurine hemisulfate; Vitamin B4 hemisulfate) Cat. No.: HY-B0152B
Adenine hemisulfate (6-Aminopurine hemisulfate) isa purine derivative with a variety of roles inbiochemistry, including cellular respiration, inthe form of both the energy-rich adenosinetriphosphate (ATP) and the cofactors nicotinamideadenine dinucleotide (NAD) and flavin…
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Adenine hydrochloride (6-Aminopurine hydrochloride; Vitamin B4 hydrochloride) Cat. No.: HY-B0152A
Adenine hydrochloride (6-Aminopurinehydrochloride) is a purine derivative with avariety of roles in biochemistry, includingcellular respiration, in the form of both theenergy-rich adenosine triphosphate (ATP) and thecofactors nicotinamide adenine dinucleotide…
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
AICAR phosphate (Acadesine phosphate; AICA Riboside phosphate) Cat. No.: HY-13417A
AICAR phosphate is an activator of AMP-activatedprotein kinase ( ).AMPK
Purity: 99.49%Clinical Data: Phase 3Size: 10 mM × 1 mL, 50 mg, 100 mg, 200 mg, 500 mg
Ajmalicine (Raubasine) Cat. No.: HY-N1919
Ajmalicine (Raubasine) is found in herbs ofCatharanthus roseus, is an antihypertensive drugused in the treatment of high blood pressure,decreases peripheral resistance and bloodpressure.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ajmaline (Cardiorythmine; (+)-Ajmaline) Cat. No.: HY-B1167
Ajmaline is an alkaloid that is class Iaantiarrhythmic agent.
Purity: 99.31%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
AkuammilineCat. No.: HY-N2834
Akuammiline, compound 2, is isolated from isolatedfrom the seeds of .Picralima klaineana
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
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Alfuzosin hydrochloride (SL 77499-10) Cat. No.: HY-B0192A
Alfuzosin hydrochloride is an α1 adrenergicreceptor antagonist used to treat benign prostatichyperplasia (BPH).
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg
AllocryptopineCat. No.: HY-N1933
Allocryptopine, a derivative oftetrahydropalmatine, is extracted from Corydalis
(Thunb.) Pers. Papaveraceae.decumbensAllocryptopine has antiarrhythmic effects andpotently blocks human ether-a-go-go related gene
current.(hERG)
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
AloperineCat. No.: HY-13516
Aloperine is an alkaloid in sophora plants such as, which has shownSophora alopecuroides L
anti-cancer, anti-inflammatory and anti-virusproperties. Aloperine is widely used to treatpatients with allergic contact dermatitis eczemaand other skin inflammation in China.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Alpha-SolamarineCat. No.: HY-N1917
Alpha-Solamarine is a glycoalkaloid isolated from.Solanum aculeastrum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ampiroxicam (CP 65703) Cat. No.: HY-17484
Ampiroxicam(CP65703) is a nonselectivecyclooxygenase inhibitor uesd as anti-inflammatorydrug. Target: COX Ampiroxicam is a non-steroidalanti-inflammatory drug. It is a prodrug ofpiroxicam.
Purity: 97.36%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg
Amsacrine hydrochloride (m-AMSA hydrochloride; acridinyl anisidide hydrochloride) Cat. No.: HY-13551A
Amsacrine hydrochloride (mAMSA hydrochloride) isan inhibitor of , and acts as antopoisomerase IIantineoplastic agent which can intercalates intothe DNA of tumor cells.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg
Ancitabine hydrochloride (Cyclocytidine hydrochloride;
Cyclo-CMP hydrochloride; Cyclo-C) Cat. No.: HY-N0093
Ancitabine (hydrochloride) is an importantantileukemia drugs.
Purity: 98.59%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 200 mg, 1 g
Anisodamine (6-Hydroxyhyoscyamine) Cat. No.: HY-N0584
Anisodamine (6-Hydroxyhyoscyamine), a belladonnaalkaloid, is a non-subtype-selective muscarinic,and also a nicotinic cholinoceptor antagonist.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Anisodamine hydrobromide (6-Hydroxyhyoscyamine hydrobromide) Cat. No.: HY-N0584A
Anisodamine hydrobromide (6-Hydroxyhyoscyaminehydrobromide), a belladonna alkaloid, is anon-subtype-selective muscarinic, and also anicotinic cholinoceptor antagonist.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ArborineCat. No.: HY-N7004
Arborine, isolated from ,Glycosmis arboreainhibits the peripheral action of acetylcholineand induces a fall in blood pressure.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
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Argatroban (MD-805; MCI-9038; Argipidine) Cat. No.: HY-B0375
Argatroban (MD-805) is a direct, selectivethrombin inhibitor.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg
Aristolochic acid A (Aristolochic acid I; TR 1736) Cat. No.: HY-N0510
Aristolochic acid A (Aristolochic acid I; TR 1736)is the main component of plant extractAristolochic acids, which are found in variousherbal plants of genus Aristolochia and .Asarum
Purity: 99.98%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 25 mg
ArmepavineCat. No.: HY-N6857
Armepavine, an active compound from Nelumbo, exerts not only anti-inflammatory effectsnucifera
on human peripheral blood mononuclear cells, butalso immunosuppressive effects on T lymphocytesand on lupus nephritic mice. Armepavine inhibitsTNF-α-induced MAPK and NF-κB signaling cascades.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ATP disodium salt (Disodium adenosine triphosphate; Adenosine
5'-triphosphate disodium salt) Cat. No.: HY-B0345A
ATP disodium salt is a phosphate-group donor forsubstrate activation in metabolic reactions andthe coenzyme for a large number of kinases.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 g, 5 g
Atropine (Tropine tropate; DL-Hyoscyamine) Cat. No.: HY-B1205
Atropine (Tropine tropate) is a competitivemuscarinic acetylcholine receptor (mAChR)antagonist with anti-myopia effect.
Purity: 99.55%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Atropine sulfate (Sulfatropinol) Cat. No.: HY-B1205A
Atropine sulfate (Sulfatropinol) is abroad-spectrum and competitive muscarinic
antagonist.acetylcholine receptor (mAChR)
Purity: >98%Clinical Data: LaunchedSize: 100 mg
Atropine sulfate monohydrate (Atropine sulfate hydrate) Cat. No.: HY-B0394
Atropine sulfate monohydrate (Atropine sulfatehydrate) is a broad-spectrum and competitivemuscarinic acetylcholine receptor (mAChR)antagonist with anti-myopia effect.
Purity: 99.62%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Azaphen (Azafen; Pipofezin hydrochloride; Pipofezine
hydrochloride) Cat. No.: HY-A0022
Pipofezine(Azafen or Azaphen) is a potentinhibitor of the reuptake of serotonin.
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 500 mg
BenazeprilCat. No.: HY-B0093
Benazepril, an angiotensin converting enzymeinhibitor, which is a medication used to treathigh blood pressure.
Purity: >98%Clinical Data: LaunchedSize: 1 g, 5 g
Benfotiamine (S-Benzoylthiamine O-monophosphate) Cat. No.: HY-17374
Benfotiamine is a synthetic S-acyl derivative ofthiamine (vitamin B1); an antioxidant dietarysupplement.
Purity: 99.58%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 g, 5 g
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Benzoylaconine (Isaconitine; Pikraconitin) Cat. No.: HY-N0217
Benzoylaconine(Isaconitine; Pikraconitin) is analkaloid in the Chinese traditional medicine RadixAconiti Lateralis Preparata (Fuzi).
Purity: 99.92%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Benzoylhypaconine (Benzoylhypacoitine) Cat. No.: HY-N0850
Benzoylhypaconine is a natural product.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Benzoylmesaconine (Mesaconine 14-benzoate) Cat. No.: HY-N0218
Benzoylmesaconine is the most abundant componentof Wutou decoction, which is widely used in Chinabecause of its therapeutic effect on rheumatoidarthritis.
Purity: 98.40%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
BerbamineCat. No.: HY-N0714
Berbamine is a natural compound extracted fromtraditional Chinese medicine Barberry withanti-tumor, immunomodulatory and cardiovasculareffects. Berbamine is a calcium channelblocker.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Berbamine dihydrochlorideCat. No.: HY-N0714A
Berbamine dihydrochloride is an inhibitor of activity with remarkable anti-myelomaNF-κB
efficacy.
Purity: 95.98%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 200 mg, 500 mg
BerberineCat. No.: HY-N0716
Berberine is a natural alkaline, reducesapoptosis, with potent anti-oxidative andanti-inflammatory effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Berberine chloride (Natural Yellow 18 chloride) Cat. No.: HY-18258
Berberine chloride is an alkaloid isolated fromthe Chinese herbal medicine Huanglian, as an
. Berberine chloride induces reactiveantibioticoxygen species ( ) generation and inhibits ROS DNA
. Antineoplastic properties.topoisomerase
Purity: 98.65%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
Berberine sulfateCat. No.: HY-N0716B
Berberine sulfate is a natural alkaline, reducesapoptosis, with potent anti-oxidative andanti-inflammatory effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Berberrubine chlorideCat. No.: HY-125850
Berberrubine chloride is an active metabolite ofberberine, attenuates ulcerative colitis in micemodel.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Betaine hydrochloride (Betaine chloride) Cat. No.: HY-N0739
Betaine hydrochloride is a natural compound foundin many foods and also an active methyl-donorwhich can maintain normal DNA methylationpatterns.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 g
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BoldineCat. No.: HY-N6973
Boldine is an aporphine isoquinoline alkaloidextracted from the root of and alsoLitsea cubebapossesses these properties, including antioxidant,anti-inflammatory and cytoprotective effects.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Brevianamide F (Cyclo(L-Pro-L-Trp)) Cat. No.: HY-100385
Brevianamide F , also known ascyclo-(L-Trp-L-Pro), belongs to a class ofnaturally occurring 2,5-diketopiperazines.
Purity: 99.49%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Brofaromine (CGP 11305A) Cat. No.: HY-13339
Brofaromine (CGP 11305A) is a monoamine oxidase( ) inhibitor with of 0.2μM forMAO IC50
.MAO-A
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg, 20 mg
Bullatine ACat. No.: HY-N5025
Bullatine A (BLA), a diterpenoid alkaloid of the, possesses anti-rheumatic,genus Aconitum
anti-inflammatory and anti-nociceptive effects.
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
Bulleyaconitine ACat. No.: HY-N0239
Bulleyaconitine A is an analgesic andantiinflammatory drug isolated from Aconitumplants; has several potential targets, includingvoltage-gated Na+ channels.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg, 50 mg
CalycanthineCat. No.: HY-N5121
Calycanthine, the principal alkaloid of the orderCalycanthaceae, has been isolated from a speciesof the genus , and is a central nervousPsychotriasystem toxin, causing convulsions.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CantharidinCat. No.: HY-N0209
Cantharidin, a natural toxin isolated from beetlesin the families Meloidae and Oedemeridae, has beenreported to be toxic to some pests, including thediamondback moth.
Purity: >98.0%Clinical Data: Phase 2Size: 10 mM × 1 mL, 25 mg, 50 mg, 100 mg, 500 mg
Capsaicin ((E)-Capsaicin) Cat. No.: HY-10448
Capsaicin ((E)-Capsaicin) is a agonist withTRPV1an of 0.29 μM in HEK293 cells.EC50
Purity: 98.39%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
CarpaineCat. No.: HY-N7016
Carpaine is an alkaloid isolated from Carica papayaLinn with activity,anti-thrombocytopenicexhibits potent activity in sustaining plateletcounts with no acute toxicity. Carpaine has
activity to prevent malaria.anti-plasmodial
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CastanospermineCat. No.: HY-N2022
Castanospermine inhibits all forms of α- andβ-glucosidases, especially glucosidase l (requiredfor glucoprotein processing by transfer of mannoseand glucose from asparagine-linked lipids).targetα- and β-glucosidases.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
10 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Catharanthine ((+)-3,4-Didehydrocoronaridine) Cat. No.: HY-N0252
Catharanthine is an alkaloid isolated from, inhibitsMadagascar periwinkle
, withvoltage-operated L-type Ca channel2+
anti-cancer and blood pressure-lowering activity.
Purity: 98.66%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg
Catharanthine Tartrate ((+)-3,4-Didehydrocoronaridine Tartrate) Cat. No.: HY-N0252A
Catharanthine Tartrate is an alkaloid isolatedfrom , inhibitsMadagascar periwinkle
, withvoltage-operated L-type Ca channel2+
anti-cancer and blood pressure-lowering activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Caulophylline BCat. No.: HY-N6672
Caulophylline B is a fluorenone alkaloid isolatedfrom the roots of Caulophyllum robustumMaxim, affords a low scavenging effect againstDPPH radical.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CefaclorCat. No.: HY-B0198
Cefaclor is an effective antibiotic agent, andspecifically binds to penicillin-binding protein 3( ).PBP 3
Purity: 96.18%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 g, 5 g
Cefsulodin sodiumCat. No.: HY-13588
Cefsulodin sodium salt hydrate is a thirdgeneration β lactam antibiotic and member of thecephems subgroub of antibiotics.
Purity: 96.50%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Ceftibuten (Sch 39720) Cat. No.: HY-B0698
Ceftibuten(Sch39720) is a third-generationcephalosporin antibiotic.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg
Celgosivir (MBI 3253; MDL 28574; MX3253) Cat. No.: HY-16134
Celgosivir (MBI 3253; MDL 28574; MX3253) is an inhibitor; inhibits bovine viralα-glucosidase I
diarrhoea virus (BVDV) with an of 1.27 μM inIC50
assay.in vitro
Purity: >98%Clinical Data: Phase 2Size: 1 mg, 5 mg, 10 mg, 25 mg, 50 mg
CephaelineCat. No.: HY-N4118
Cephaeline is a phenolic alkaloid in Indian Ipecacroots. Cephaeline exhibits potent inhibition ofboth Zika virus (ZIKV) and Ebola virus (EBOV)infections.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Cephalotaxlen ((-)-Cephalotaxine; ZINC19795976) Cat. No.: HY-N0838
Cephalotaxine is an antiviral as well as antitumoragent.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
CepharanthineCat. No.: HY-N6972
Cepharanthine, an alkaloid derived from Stephania Hayata, with possessescepharantha
anti-inflammatory and antioxidative activities.Cepharanthine attenuates muscle and kidneyinjuries induced by limb ischemia/reperfusion(I/R).
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 11
CetirizineCat. No.: HY-17042
Cetirizine, a second-generation antihistamine, isa major metabolite of hydroxyzine, and a racemicselective H1 receptor inverse agonist used in thetreatment of allergies, hay fever, angioedema, andurticaria.
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 200 mg, 500 mg
ChaetocinCat. No.: HY-N2019
Chaetocin is a specific inhibitor of the histonemethyltransferase ( ) SU(VAR)3-9 with an HMT IC50
of 0.6 μM for SU(VAR)3-9. It also inhibitsthioredoxin reductase ( ) with an of 4TrxR IC50
μM.
Purity: 98.06%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
ChasmanineCat. No.: HY-N1946
Chasmanine is an alkaloid isolated from the rootsof .Aconitum crassicaule
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ChelerythrineCat. No.: HY-N2359
Chelerythrine is a natural alkaloid, acts as apotent and selective Ca /phospholopid-dependent2+
antagonist, with an of 0.7 μM.PKC IC50
Chelerythrine has antitumor, antidiabetic andanti-inflammatory activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Chelerythrine ChlorideCat. No.: HY-12048
Chelerythrine Chloride is a potent, cell-permeableinhibitor of , with an of 660protein kinase C IC50
nM.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
ChelidonineCat. No.: HY-N2369
Chelidonine is an isoquinoline alkaloid isolatedfrom , causes G arrestChelidonium majus L. 2/M
and induces caspase-dependent andcaspase-independent , with anticancer andapoptosisantiviral activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Chimonanthine ((-)-Chimonanthine) Cat. No.: HY-N5118
Chimonanthine is an alkaloid of Chimonanthus, inhibits tyrosinase and tyrosine-relatedpraecox
protein-1 mRNA expression, amd inhibitsmelanogenesis.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Cinchonidine (α-Quinidine) Cat. No.: HY-N0173
Cinchonidine (α-Quinidine) is a cinchona alkaloidfound in Cinchona officinalis and Gongronemalatifolium. A building block used in asymmetricsynthesis in organic chemistry.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Cinchonine ((8R,9S)-Cinchonine; LA40221) Cat. No.: HY-Y0152
Cinchonine is a natural compound present inCinchona bark. Cinchonine activates endoplasmicreticulum stress-induced apoptosis in human livercancer cells.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
CinobufotalinCat. No.: HY-N0880
Cinobufotalin is one of the bufadienolidesprepared from toad venom; has anticancer activity.IC50 value: Target: in vitro: Cinobufotalin(CB)caused significant DNA fragmentation, decrease ofMMP, and an increase in the intracellular Ca(2+)ion and ROS production.
Purity: 99.70%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg
12 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
ColchicineCat. No.: HY-16569
Colchicine is a inhibitor and atubulin disrupting agent. Colchicinemicrotubule
inhibits microtubule polymerization with an IC50
of 3 nM.
Purity: 99.98%Clinical Data: LaunchedSize: 10 mM × 1 mL, 200 mg, 500 mg
Columbamine (Columbamin; Dehydroisocorypalmine) Cat. No.: HY-N0926
Columbamine is a quaternary isoquinoline alkaloidisolated from Argemone mexicana.
Purity: 98.38%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Coptisine (Coptisin) Cat. No.: HY-N0430
Coptisine is an alkaloid from Chinese goldthread,and acts as an efficient uncompetitive IDOinhibitor with a value of 5.8 μM and an Ki IC50
value of 6.3 μM.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg, 50 mg
Coptisine chlorideCat. No.: HY-N0736
Coptisine chloride is an alkaloid from Chinesegoldthread, and acts as an efficient uncompetitive
inhibitor with a value of 5.8 μM and an IDO Ki IC50
value of 6.3 μM.
Purity: 99.29%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Coptisine SulfateCat. No.: HY-N0430A
Coptisine Sulfate is an alkaloid from Chinesegoldthread, and acts as an efficient uncompetitive
inhibitor with a value of 5.8 μM and an IDO Ki IC50
value of 6.3 μM.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Cordycepin (3'-Deoxyadenosine) Cat. No.: HY-N0262
Cordycepin, which is a nucleoside derivativeisolated from , inhibits IL-1β-inducedCordyceps
and expression in rheumatoidMMP-1 MMP-3arthritis synovial fibroblasts (RASFs) in adose-dependent manner.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 25 mg, 50 mg
Corydaline ((+)-Corydaline; Corydalin) Cat. No.: HY-N0923
Corydaline is an acetylcholinesterase inhibitorisolated from Corydalis yanhusuo.
Purity: 96.17%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
CorydineCat. No.: HY-N2571
Corydine is a naturally occurring alkaloid whichcan be extracted from plants such as Croton
leaves. Corydine is efficient onechinocarpusinhibiting (RT) activityreverse transcriptasewith an IC of 356.8 μg/mL.50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CorynolineCat. No.: HY-N0826
Corynoline, isolated from Corydalis incise(Papaveraceae), is a reversible and noncompetitiveacetylcholinesterase ( ) inhibitor with anAChE
of 30.6 μM. Corynoline exhibitsIC50
anti-inflammatory activity by activating .Nrf2
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CorynoxeineCat. No.: HY-N0590
Corynoxeine, isolated from the hook of Uncaria, is a potent / inhibitor ofrhynchophylla ERK1 ERK2
key PDGF-BB-induced vascular smooth muscle cells(VSMCs) proliferation.
Purity: 99.91%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
www.MedChemExpress.com 13
CorynoxineCat. No.: HY-N0901
Corynoxine is an enantiomer of Corynoxine B;induces autophagy in different neuronal celllines, including N2a and SHSY-5Y cells.
Purity: 99.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Corynoxine BCat. No.: HY-N0901A
Corynoxine B is an oxindole alkaloid isolated fromUncaria rhynchophylla (Miq.) Jacks (Gouteng inChinese); a Beclin-1-dependent autophagy inducer.
Purity: 99.76%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
CorypalmineCat. No.: HY-N0654
Corypalmine is an alkaloid from Corydalis. Corypalmine is an antifungal.chaerophylla
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CorytuberineCat. No.: HY-N2570
Corytuberine is an aporphine alkaloid isolatedfrom . CorytuberineDicranostigma leptopodumdisplays cytotoxicity against SMMC-7721 tumorcells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Cotinine ((-)-Cotinine; (S)-Cotinine; NIH-10498) Cat. No.: HY-B1178
Cotinine is an alkaloid found in tobacco and isalso the predominant metabolite of nicotine, usedas a biomarker for exposure to tobacco smoke.
Purity: 99.42%Clinical Data: Phase 2Size: 10 mM × 1 mL, 50 mg, 100 mg
Crassicauline A (Crassicaulin A) Cat. No.: HY-N1924
Crassicauline A (Crassicaulin A) is a bioactivealkaloid found in roots of Aconitum
. Crassicauline A (Crassicaulin A)carmichaelipossesses feeding deterrent activity against T.
adults with an EC of 1134.5 ppm.castaneum 50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Creatinine (NSC13123) Cat. No.: HY-B0504
Creatinine(NSC13123) is a break-down product ofcreatine phosphate in muscle, and is usuallyproduced at a fairly constant rate by the body.
Purity: >99.0%Clinical Data: Phase 4Size: 10 mM × 1 mL, 1 g, 5 g
CrebanineCat. No.: HY-N2255
Crebanine, an alkaloid from ,Stephania venosainduces G1 arrest and apoptosis in human cancercells. Crebanine exhibits anti-inflammatoryactivity via suppressing MAPKs and Akt signaling.Crebanine also possesses antiarrhythmic effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Crotonoside (Isoguanosine) Cat. No.: HY-N0071
Crotonoside is isolated from Chinese medicinalherb, Croton. Crotonoside inhibits andFLT3
, exhibits selective inhibition in acuteHDAC3/6myeloid leukemia (AML) cells. Crotonoside could bea promising new lead compound for the treatment ofAML.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Cyclovirobuxine DCat. No.: HY-N0107
Cyclovirobuxine D (CVB-D) is the main activecomponent of the traditional Chinese medicine Buxus
. Cyclovirobuxine D inducesmicrophylla and attenuates the phosphorylation of autophagy
and .Akt mTOR
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
14 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Cytidine (Cytosine β-D-riboside; Cytosine-1-β-D-ribofuranoside) Cat. No.: HY-B0158
Cytidine is a nucleoside molecule that is formedwhen cytosine is attached to a ribose ring,cytidine is a component of RNA.
Purity: 98.97%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 g, 5 g
Cytisinicline (Cytisine; Sophorine; Baptitoxine) Cat. No.: HY-N0175
Cytisinicline (Cytisine) is an alkaloid thatoccurs naturally in several plant genera, such as
and . Cytisinicline (Cytisine)Laburnum Cytisusis a partial agonist of , and partialα4β2 nAChRsto full agonist at β4 containing receptors and α7receptors.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 25 mg
Danofloxacin mesylate (CP 76136-27) Cat. No.: HY-B0501
Danofloxacin mesylate (CP 76136-27) is afluoroquinolone antibacterial for veterinary use.
Purity: 99.59%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
DauricineCat. No.: HY-N0220
Dauricine, a bisbenzylisoquinoline alkaloid in, possessesAsiatic Moonseed Rhizome
anti-inflammatory activity. Dauricine inhibitscell proliferation and invasion, and inducesapoptosis by suppressing activation in aNF-κBdose- and time-dependent manner in colon cancer.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Daurisoline ((R,R)-Daurisoline) Cat. No.: HY-N0221
Daurisoline is a inhibitor and also anhERG blocker.autophagy
Purity: 98.02%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
Dehydrocorydaline (13-Methylpalmatine) Cat. No.: HY-N0674
Dehydrocorydaline (13-Methylpalmatine) is analkaloid isolated from traditional Chinese herb
W.T. Wang. DehydrocorydalineCorydalis yanhusuoregulates protein expression of , ;Bax Bcl-2activates , , and inactivatescaspase-7 caspase-8
.PARP
Purity: >98%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Dehydrocorydaline chloride (13-Methylpalmatine chloride) Cat. No.: HY-N0674A
Dehydrocorydaline chloride is an alkaloidal thathas anti-inflammatory and anti-cancer activities.Dehydrocorydaline chloride can elevate p38
activation.MAPK
Purity: 98.64%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
DehydroevodiamineCat. No.: HY-N2106
Dehydroevodiamine is a major bioactive quinazolinealkaloid isolated from , has anEvodiae Fructusantiarrhythmic effect in guinea-pig ventricularmyocytes.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DehydrotomatineCat. No.: HY-N7001
Dehydrotomatine is one of major steroidalglycoalkaloids (SGAs) that accumulate in themature green fruits, leaves and flowers of tomato( ). Dehydrotomatine isSolanum lycopersicumagainst , fungi, insects and animals.bacteria
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
Delavirdine (U 90152; BHAP-U 90152) Cat. No.: HY-10571
Delavirdine(U 90152) is a potent non-nucleosidereverse transcriptase inhibitor (NNRTI).
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg, 200 mg
www.MedChemExpress.com 15
DelsolineCat. No.: HY-N0789
Delsoline, a major alkaloid of Delphinium, has both a curare-likeanthriscifolium Hance
effect and a ganglion-blocking effect and is usedto relieve muscle tension or hyperkinesia. D.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DeltalineCat. No.: HY-N0329
Deltaline is a diterpenoid alkaloid and isolatedfrom plants of the genus Delphinium delavayiFranch.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DendrobineCat. No.: HY-N0638
Dendrobine is an alkaloid isolated from. Dendrobine possessesDendrobium nobile
antiviral activity against , withinfluenza A virusess of 3.39 μM, 2.16 μM and 5.32 μM forIC50
A/FM-1/1/47 (H1N1), A/Puerto Rico/8/34 H274Y(H1N1) and A/Aichi/2/68 (H3N2), respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DenudatineCat. No.: HY-N1982
Denudatine, is primarily isolated from plants ofthe genera Aconitum and Delphinium. Denudatine haseffects on action potential of ventricular fibersand inhibits arrhythmogenic action of aconitine.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Desmethylglycitein (4',6,7-Trihydroxyisoflavone) Cat. No.: HY-N5072
Desmethylglycitein (4',6,7-Trihydroxyisoflavone),a metabolite of daidzein, sourced from Glycine
with antioxidant, and anti-cancermaxactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DetomidineCat. No.: HY-B0163
Detomidine produce dose-dependent sedative andanalgesic effects, is a nonnarcotic, syntheticα2-adrenergic agonist.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg
DicentrineCat. No.: HY-N6969
Dicentrine is a natural product isolated from theplant with antihypertensiveLindera megaphyllaeffect. Dicentrine is an α -adrenoceptor1
antagonist which has effective against humanhyperplastic prostates.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Dictamine (Dictamnine; Dectamine) Cat. No.: HY-N0849
Dictamnine (Dictamine) has the ability to exertcytotoxicity in human cervix, colon, and oralcarcinoma cells; A natural plant product has beenreported to have antimicrobial activity againstbacteria and fungi.
Purity: 98.87%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Dihydralazine sulfateCat. No.: HY-N7065
Dihydralazine sulfate is an antihypertensiveagent.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DihydrocapsaicinCat. No.: HY-N0361
Dihydrocapsaicin is a natural capsaicin, acts as aselective agonist, and also increases p-AktTRPV1levels. Dihydrocapsaicin enhances thehypothermia-induced neuroprotection.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
16 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Dihydrochelerythrine (12,13-Dihydrochelerythrine) Cat. No.: HY-N0903
Dihydrochelerythrine is a natural compoundisolated from the leaves of Macleaya microcarpa;has antifungal activity. IC50 value: Target: invitro: Dihydrochelerythrine showed the highestantifungal activity against B.
Purity: 99.39%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
DihydrolycorineCat. No.: HY-N2403
Dihydrolycorine is isolated from Lycoris radiateHerb with antihypertensive and neuroprotectiveactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DihydropalmatineCat. No.: HY-N4240
Dihydropalmatine is a alkaloid isolated from.Berberis aristata
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Dihydrosanguinarine (13,14-Dihydrosanguinarine) Cat. No.: HY-N0902
Dihydrosanguinarine is a natural compound isolatedfrom the leaves of Macleaya microcarpa; hasantifungal and anticancer activity.
Purity: 99.80%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Dobutamine hydrochlorideCat. No.: HY-15746
Dobutamine hydrochloride is a sympathomimetic drugused in the treatment of heart failure andcardiogenic shock. Its primary mechanism is directstimulation of β1 receptors of the sympatheticnervous system.
Purity: 99.78%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Doxazosin (UK 33274) Cat. No.: HY-B0098
Doxazosin(UK 33274) is a quinazoline-derivativethat selectively antagonizes postsynapticα1-adrenergic receptors.
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 500 mg
Ecteinascidin 770 (Ecteinascidine 770; Et-770) Cat. No.: HY-101191
Ecteinascidin 770 (ET-770) is a1,2,3,4-tetrahydroisoquinoline alkaloid withpotent anti-cancer activities; inhibits U373MGcells with an of 4.83 nM.IC50
Purity: 98.82%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg
Efavirenz (DMP 266; EFV; L-743726) Cat. No.: HY-10572
Efavirenz is a potent inhibitor of the wild-type with a of 2.93 nM andHIV-1 reverse transcriptase Ki
exhibits an of 1.5 nM for the inhibition ofIC95
HIV-1 replicative spread in cell culture.
Purity: 99.99%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Ellipticine (NSC 71795) Cat. No.: HY-15753
Ellipticine (NSC 71795) is a potent antineoplasticagent; inhibits activities.DNA topoisomerase II
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 50 mg, 100 mg
Ellipticine hydrochloride (NSC 71795 (hydrochloride)) Cat. No.: HY-15753A
Ellipticine (NSC 71795) hydrochloride is a potentantineoplastic agent; inhibits DNA topoisomerase
activities.II
Purity: 98.08%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
www.MedChemExpress.com 17
Emetine dihydrochlorideCat. No.: HY-B1479A
Emetine (dihydrochloride) is an anti-protozoaldrug previously used for intestinal and tissueamoebiasis.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Enniatin BCat. No.: HY-N3806
Enniatin B is a mycotoxin. Enniatin BFusariuminhibits acyl-CoA: cholesterol acyltransferase( ) activity with an of 113 μM in anACAT IC50
enzyme assay using rat liver microsomes. EnniatinsB decreases the activation of (p44/p42).ERK
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Enniatin B1Cat. No.: HY-N3807
Enniatin B1 is a mycotoxin. EnniatinFusariumB1 inhibits acyl-CoA: cholesterol acyltransferase( ) activity with an of 73 μM in anACAT IC50
enzyme assay using rat liver microsomes. EnniatinB1 crosss the blood-brain barrier.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
EpiberberineCat. No.: HY-N0226
Epiberberine is an alkaloid isolated from Coptis, acts as a potent and chinensis AChE BChE
inhibitor, and a non-competitive inhibitor,BACE1with s of 1.07, 6.03 and 8.55 μM,IC50
respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 50 mg
Epiberberine chlorideCat. No.: HY-N0226A
Epiberberine chloride is an alkaloid isolated from, acts as a potent and Coptis chinensis AChE BChE
inhibitor, and a non-competitive inhibitor,BACE1with s of 1.07, 6.03 and 8.55 μM,IC50
respectively.
Purity: 99.60%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Etimizol (Ethimizole; Ethymisol; Ethymisole) Cat. No.: HY-13918
Etimizol(Ethymisole; Antiffine; Ethylnorantifein)was shown to relieve amnesia effectively in theorigin of which there is the hypoxic component(hypobaric hypoxia, actinomycin D, mechanicalinjury of the brain).
Purity: 99.95%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Evodiamine ((+)-Evodiamine; d-Evodiamine) Cat. No.: HY-N0114
Evodiamine is an alkaloid isolated from the fruitof Bentham with diverse biologicalEvodia rutaecarpaactivities including anti-inflammatory,anti-obesity, and antitumor.
Purity: 99.60%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg, 200 mg
Fenspiride HydrochlorideCat. No.: HY-A0027
Fenspiride Hcl is an α adrenergic and H1 histaminereceptor antagonist.
Purity: 99.03%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Flaconitine (Acetylaconitine; 3-Acetylaconitine) Cat. No.: HY-N0276
Flaconitine is isolated from the ammoniumhydroxide wetted root of Gay.A.szechenyianumFlaconitine is considered to be a NF-κBinhibitor.
Purity: >98%Clinical Data: LaunchedSize: 5 mg, 10 mg
Flupirtine (D 9998) Cat. No.: HY-17001A
Flupirtine(D 9998) is a selective neuronalpotassium channel opener that also has NMDAreceptor antagonist properties.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg, 500 mg
18 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Fluvoxamine (DU-23000) Cat. No.: HY-B0103
Fluvoxamine (DU-23000) is an antidepressant whichfunctions pharmacologically as a selectiveserotonin reuptake inhibitor.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg
Foresaconitine (Vilmorrianine C) Cat. No.: HY-N0851
Foresaconitine(Vilmorrianine C) is anorditerpenoid alkaloid isolated from theprocessed tubers of Aconitum carmichaeli.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Fosinopril sodium (SQ28555) Cat. No.: HY-B0382
Fosinopril Sodium is the ester prodrug of anangiotensin-converting enzyme (ACE) inhibitor,used for the treatment of hypertension and sometypes of chronic heart failure.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
Fumitremorgin C (12α-Fumitremorgin C) Cat. No.: HY-N2143
Fumitremorgin C is a potent and selective inhibitor.ABCG2/BRCP
Purity: 99.63%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 250 μg, 1 mg
Galanthamine (Galantamine) Cat. No.: HY-76299
Galanthamine is a potent acetylcholinesterase( ) inhibitor with an of 500 nM.AChE IC50
Purity: 99.90%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
Galanthamine hydrobromide (Galantamine hydrobromide) Cat. No.: HY-A0009
Galanthamine hydrobromide is a long-acting,centrally active acetylcholinesterase(AChE)inhibitor (IC50 = 410 nM) and allostericpotentiator at neuronal nicotinic ACh receptors.
Purity: 99.93%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
Gatifloxacin hydrochloride (AM 1155 hydrochloride; BMS
206584-01 hydrochloride; PD 135432 hydrochloride) Cat. No.: HY-10581A
Gatifloxacin (hydrochloride) is an antibiotic ofthe fourth-generation fluoroquinolone family, itinhibits the bacterial enzymes DNA gyrase andtopoisomerase IV.
Purity: >98%Clinical Data: LaunchedSize: 1 g, 5 g
Geissoschizine methyl etherCat. No.: HY-N2411
Geissoschizine methyl ether, a major indolealkaloid found in hook, is a major activeUncariacomponent of Yokukansan with psychotropic effects.Geissoschizine methyl ether is potent 5-HT1A
agonist.receptor
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
GelsemineCat. No.: HY-N0388
Gelsemine, an alkaloid from the Chinese herb, is effective in mitigatingGelsemium elegans
chronic pain. Antinociceptive and hypnoticeffects.
Purity: 99.50%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Glycoursodeoxycholic acid (Ursodeoxycholylglycine) Cat. No.: HY-N1424
Glycoursodeoxycholic acid, a acyl glycine and abile acid-glycine conjugate, is a metabolite ofursodeoxycholic acid.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
www.MedChemExpress.com 19
Gramine (Donaxine) Cat. No.: HY-N0166
Gramine (Donaxine) is a natural alkaloid isolatedfrom giant reed, acts as an active adiponectin
agonist, with s of 3.2 andreceptor (AdipoR) IC50
4.2 µM for AdipoR2 and AdipoR1, respectively.Gramine is also a human and mouse β2-Adrenergic
agonist.receptor (β2-AR)
Purity: 99.45%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg
Granisetron (BRL 43694) Cat. No.: HY-B0071
Granisetron (BRL 43694) is a serotonin 5-HT3receptor antagonist used as an antiemetic to treatnausea and vomiting following chemotherapy.
Purity: >98%Clinical Data: LaunchedSize: 50 mg, 100 mg
Guvacine hydrochlorideCat. No.: HY-100809
Guvacine hydrochloride is an alkaloid from the nutof , acts as an inhibitor of Areca catechu GABA
, and dispalys modest selectivity fortransportercloned GABA transporters with s of 14 μMIC50
(human GAT-1), 39 μM (rat GAT-1), 58 μM (ratGAT-2), 119 μM (human GAT-3), 378 μM (rat…
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Halofuginone (RU-19110) Cat. No.: HY-N1584
Halofuginone (RU-19110) is a less-toxic form ofFebrifugine, which is isolated from the plant
. Halofuginone inhibits Dichroa febrifuga prolyl-tRNA in an ATP-dependent manner with a synthetase Ki
of 18.3 nM. Halofuginone attenuates osteoarthritis(OA) by inhibition of activity.TGF-β
Purity: 98.32%Clinical Data: Phase 2Size: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Halofuginone hydrobromide (RU-19110 (hydrobromide)) Cat. No.: HY-N1584A
Halofuginone hydrobromide (RU-19110 hydrobromide)is a less-toxic form of Febrifugine, which isisolated from the plant .Dichroa febrifugaHalofuginone inhibits in anprolyl-tRNA synthetaseATP-dependent manner with a of 18.3 nM.Ki
Purity: 99.94%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
Harmine (Telepathine) Cat. No.: HY-N0737A
Harmine is a natural dual-specificity tyrosinephosphorylation-regulated kinase ( )(DYRK)inhibitor with anticancer and anti-inflammatoryactivities.
Purity: 99.78%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 500 mg
HarringtonineCat. No.: HY-N0862
Harringtonine is a natural alkaloidCephalotaxusthat inhibits .protein synthesis
Purity: 99.91%Clinical Data: Phase 3Size: 10 mM × 1 mL, 5 mg, 10 mg
HirsuteineCat. No.: HY-N2197
Hirsuteine is an indole alkaloid extracted from. Hirsuteine non-competitivelyUncaria genus
antagonizes nicotine-mediated dopamine release byblocking ion permeation through nicotinic receptorchannel complexes.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
HirsutineCat. No.: HY-N2193
Hirsutine, an indole alkaloid of Uncaria, exhibits anti-cancer activity.rhynchophylla
Hirsutine induces apoptosis and is a potent Denguevirus inhibitor exhibiting low cytotoxicity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Homoharringtonine (Omacetaxine mepesuccinate; HHT) Cat. No.: HY-14944
Homoharringtonine (Omacetaxine mepesuccinate;HHT)is a cytotoxic alkaloid with antitumor propertieswhich acts by inhibiting .translation elongation
Purity: 99.96%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg
20 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Hydrastine ((-)-β-Hydrastine; (1R,9S)-β-Hydrastine) Cat. No.: HY-B0927
Hydrastine is a natural alkaloid which is presentin Hydrastis canadensis and other plants of theranunculaceae family.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
HydroprotopineCat. No.: HY-N2483
Hydroprotopine is a alkaloid from Hypecoum. Leptopidine can suppress growthleptocarpumand
and induce cytotoxicity in breast cancer cells andthat the cytotoxicity of leptopidine may berelated to its inhibitory effect on fatty acidsynthase expression.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Hydroxy-β-sanshoolCat. No.: HY-N6824
Hydroxy-β-sanshool is an alkylamide exists inZanthoxylum bungeanum oil and Zanthoxylumschinifolium oil.
Purity: 99.36%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg
Hydroxy-γ-sanshoolCat. No.: HY-N6823
Hydroxy-γ-sanshool is an alkylamide exists inZanthoxylum bungeanum oil and Zanthoxylumschinifolium oil.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Hydroxy-α-sanshoolCat. No.: HY-N6825
Hydroxy-α-sanshool is an alkylamide isolatedfrom , acts as a covalent and pepper TRPA1 TRPV1non-covalent agonist, with s of 69 and 1.1EC50
µM, respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
HypaconitineCat. No.: HY-N0267
Hypaconitine, an active and highly toxicconstituent derived from Aconitum species, iswidely used to treat rheumatism.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Hypoxanthine (Purin-6-ol; Sarcine) Cat. No.: HY-N0091
Hypoxanthine, a purine derivative, is a potentialfree radical generator and could be used as anindicator of hypoxia.
Purity: 99.94%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg
Indaconitine (15-Deoxyaconitine) Cat. No.: HY-N0788
Indaconitine is a natural product.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Indirubin (Couroupitine B; Indigo red; Indigopurpurin) Cat. No.: HY-N0117
Indirubin (Couroupitine B) is a purple 3,2-bisindole and a stable isomer of indigo isolatedfrom Indigo naturalis (Apiaceae);anti-inflammatory and anticancer activities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 250 mg
Indole-3-butyric acid (3-indolebutyric acid) Cat. No.: HY-N0186
Indole-3-butyric acid (3-indolebutyric acid; IBA)is a plant growth auxin and a good rooting agent.It can promote herbs and woody ornamental plantrooting and used for improving fruit rate.
Purity: 99.66%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 g, 10 g
www.MedChemExpress.com 21
Indole-3-carbinol (I3C; 3-Indolemethanol) Cat. No.: HY-N0170
Indole-3-carbinol (I3C) inhibits activityNF-κBand also is an ( )Aryl hydrocarbon receptor AhRagonist, and an inhibitor of (WWWWP1domain-containing ubiquitin E3 ligase 1).
Purity: >98.0%Clinical Data: Phase 2Size: 10 mM × 1 mL, 200 mg, 1 g
Isatin (Indoline-2,3-dione) Cat. No.: HY-Y0265
Isatin (Indoline-2,3-dione) is a potent inhibitorof with an of 3monoamine oxidase (MAO) IC50
μM. Also binds to central benzodiazepine receptors(IC against clonazepam, 123 μM).50
Purity: >97.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Isocorynoxeine (7-Isocorynoxeine) Cat. No.: HY-N0775
Isocorynoxeine, an isorhynchophylline-relatedalkaloid, exhibits a dose-dependent inhibition of
receptor-mediated current response with5-HT2A
an of 72.4 μM.IC50
Purity: 99.97%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
IsorhynchophyllineCat. No.: HY-N0766
Isorhynchophylline (IRN), an alkaloid isolatedfrom Uncaria rhynchophylla, possesses the effectsof lowered blood pressure, vasodilatation andprotection against ischemia-induced neuronaldamage.
Purity: 99.90%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Isovaleramide (3-Methylbutanamide) Cat. No.: HY-B1229
Isovaleramide is an active principle on centralnervous system from Valeriana pavonii, as ananticonvulsant. Target in vitro: Isovaleramide(300 μM) exhibits a 42% of inhibition of thebinding of 3H-FNZ to its sites. in vivo:Isovaleramide at 100 mg/Kg, p.
Purity: >98%Clinical Data: No Development ReportedSize: 100 mg
Jervine (11-Ketocyclopamine) Cat. No.: HY-N0836
Jervine(11-Ketocyclopamine) is a naturallyoccuring steroidal alkaloid that causes cyclopiaby blocking sonic hedgehog(Shh) signaling; Jervineis an inhibitor of Smo. IC50 value: Target: sonichedgehog is derived from the Veratrum plantspecies.
Purity: 99.03%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 50 mg
KaracolineCat. No.: HY-N6812
Karacoline, a diterpene alkaloid found in theplant , reduces degradationAconitum kusnezoffiiof the extracellular matrix (ECM) inintervertebral disc degeneration (IDD) via theNF-κB signaling pathway.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ketanserin tartrate (R41468 tartrate) Cat. No.: HY-10562A
Ketanserin tartrate is a selective 5-HT receptorantagonist. Ketanserin tartrate also blocks hERGcurrent ( ) in a concentration-dependentIhERG
manner ( =0.11 μM).IC50
Purity: 99.97%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
Kinetin (6-Furfuryladenine; N6-Furfuryladenine) Cat. No.: HY-N0160
Kinetin (N6-furfuryladenine) belongs to a group ofplant growth hormones involved in cell division,differentiation and other physiological processes.
Purity: 99.72%Clinical Data: Phase 4Size: 10 mM × 1 mL, 1 g, 5 g
KoumineCat. No.: HY-N1440
Koumine is an alkaloid separated from Gelsemium, shows potent anti-tumor activity. Koumineelegans
up-regulates the Bax/Bcl-2 ratio and caspase-3expression in human breast cancer cells.
Purity: 99.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
22 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Kukoamine ACat. No.: HY-N2392
Kukoamine A is a natural occurring sperminederivative, acts as a potent inhibitor of
( , 1.8 μM), withtrypanothione reductase Ki
antihypertensive activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Kukoamine BCat. No.: HY-N2393
Kukoamine B is a component of Lycii Cortex, withanti-oxidant, anti-acute inflammatory andanti-diabetic properties.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
L-(+)-Abrine (L-Abrine; L-N-Methyltryptophan; N-α-Methyl-L-tryptophan) Cat. No.: HY-N1436
L-(+)-Abrine, a lethal albumin found in Abrus seeds, is an acute toxic alkaloid andprecatorius
chemical marker for abrin.
Purity: >98%Clinical Data: No Development ReportedSize: 100 mg
L-DOPA (Levodopa; 3,4-Dihydroxyphenylalanine) Cat. No.: HY-N0304
L-DOPA is a natural form of DOPA used in thetreatment of Parkinson's disease. L-DOPA is theprecursor of dopamine and product of tyrosinehydroxylase.
Purity: 99.83%Clinical Data: LaunchedSize: 200 mg, 1 g
L-Hyoscyamine (Daturine) Cat. No.: HY-N0471
L-Hyoscyamine is a chemical compound, a tropanealkaloid it is the levo-isomer to atropine.
Purity: 99.32%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 500 mg
L-Praziquanamine ((+)-Praziquanamine) Cat. No.: HY-N1765
L-Praziquanamine is a natural product.
Purity: 99.92%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
L-Stepholidine (Stepholidine; (-)-Stepholidine; L-SPD) Cat. No.: HY-N6960
L-Stepholidine (Stepholidine), an alkaloid extractof the Chinese herb , is theStephania intermediafirst compound known to exhibit mixed dopamine
agonist/D2 antagonist properties.D1 receptor
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lappaconitine ((+)-Lappaconitine) Cat. No.: HY-N0383
Lappaconitine, isolated from Aconitum sinomontanumNakai, was characterized as analgesic principle.IC50 value: Target: In vitro: In vivo:Lappaconitine was characterized as analgesicprinciple by our laboratory.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg, 50 mg, 100 mg
Lappaconitine hydrobromide (Allapinine) Cat. No.: HY-N0118
Lappaconitine hydrobromide, a diterpene alkaloid,is a drug for the treatment of cardiacarrhythmias.
Purity: >95.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Latrunculin A (LAT-A) Cat. No.: HY-16929
Latrunculin A (LAT-A) is a toxin isolated from thered sea sponge , binds toLatrunculia magnificaactin monomers, inhibits polymerization of actin,with s of 0.1, 0.4, 4.7 μM and 0.19 μM forKd
ATP-actin, ADP-Pi-actin, ADP-actin and G-actin,respectively.
Purity: >95.0%Clinical Data: No Development ReportedSize: 100 μg
www.MedChemExpress.com 23
Laurolitsine hydrochloride ((+)-Norboldine hydrochloride) Cat. No.: HY-N2352A
Laurolitsine hydrochloride is an alkaloid isolatedfrom , and shows weakPhoebe formosanaanti-inflammatory activity.
Purity: 99.81%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
Leonurine (SCM-198) Cat. No.: HY-N0741
Leonurine is an alkaloid isolated from Herba, with anti-oxidative and anti-inflammatory.leonuri
Purity: 99.62%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Leonurine hydrochloride (SCM-198 hydrochloride) Cat. No.: HY-N0741A
Leonurine hydrochloride is an alkaloid isolatedfrom , with anti-oxidative andHerba leonurianti-inflammatory.
Purity: 99.66%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Levoleucovorin Calcium (Calcium levofolinate; CL307782) Cat. No.: HY-13667
Levoleucovorin calcium is the calcium salt ofLevoleucovorin, which is the enantiomericallyactive form of folinic acid.
Purity: 95.24%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg, 1 g, 2 g
Ligustrazine hydrochloride (Chuanxiongzine hydrochloride;
Tetramethylpyrazine hydrochloride) Cat. No.: HY-N0935
Ligustrazine (hydrochloride) is a natural product.IC50 value: Target: In vitro: Ligustrazinehydrochloride displayed a protection effect oninjured ECV304 cells, NOS and NO formation weresignificantly increased compared with the modelgroup . In vivo:.
Purity: 99.93%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Lisinopril (MK-521) Cat. No.: HY-18206
Lisinopril (MK-521) is angiotensin-convertingenzyme inhibitor, used in treatment ofhypertension, congestive heart failure, and heartattacks.
Purity: >98%Clinical Data: LaunchedSize: 1 g, 5 g
Lobeline hydrochloride (α-Lobeline hydrochloride; L-Lobeline hydrochloride) Cat. No.: HY-B0979
Lobeline hydrochloride, a nicotinic receptoragonist, acting as a potent antagonist at bothα3β2 and α4β2 neuronal nicotinic receptorsubtypes.
Purity: 99.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
LudaconitineCat. No.: HY-N6816
Ludaconitine, isolated from Aconitum (Bruhl) Stapf, exhibitsspicatum
antileishmanial activity with an IC of 36.1050
μg/mL.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lycorine hydrochlorideCat. No.: HY-N0289
Lycorine (hydrochloride) is VE-cadherininhibitor,and has IC50 of 1.2μM in Hey1B cell.
Purity: 99.89%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 25 mg, 50 mg, 100 mg
LysergolCat. No.: HY-N6809
Lysergol, a clavine alkaloid isolated from seedsof , is a bioenhancer forIpomoea muricatathe drugs and nutrients and has antibacterialactivity. Lysergol has been used as hypotensive,psychotropic analgesic and uterus- andintestine-stimulating drug.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
24 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Matrine (Matridin-15-one; Vegard; α-Matrine) Cat. No.: HY-N0164
Matrine (Matridin-15-one) is an alkaloid found inplants from the Sophora genus. It has a variety ofpharmacological effects, including anti-cancereffects, and action as a kappa opioid receptor andu-receptor agonist.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 200 mg, 500 mg
MedetomidineCat. No.: HY-17034
Medetomidine(Domtor) is a potent, highly selectiveα2-adrenoceptor agonist (Ki values are 1.08 and1750 nM for α2- and α1-adrenoceptorsrespectively).
Purity: 99.88%Clinical Data: LaunchedSize: 5 mg, 10 mg, 50 mg
MeleagrinCat. No.: HY-N6797
Meleagrin is a roquefortine C-derived alkaloidproduced by fungi of the genus andPenicilliumhas antimicrobial and anti-proliferativeactivities. Meleagrin is a class of inhibitor.FabI
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Meropenem (SM 7338) Cat. No.: HY-13678
Meropenem (SM 7338) is a carbapenem antibiotic,which displaying a broad spectrum of antibacterialactivity.
Purity: >98%Clinical Data: LaunchedSize: 50 mg, 100 mg
MesaconineCat. No.: HY-N1922
Mesaconinean, an ingredient from Aconitum Debx., has cardiac effect.carmichaelii
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
MesaconitineCat. No.: HY-N0724
Mesaconitine is the main active component of genusaconitum plants.
Purity: 98.97%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mianserin hydrochloride (Org GB 94) Cat. No.: HY-B0188A
Mianserin hydrochloride is a H1 receptor inverseagonist and is a psychoactive agent of thetetracyclic antidepressant. Target: H1 receptorMianserin is a psychoactive drug of thetetracyclic antidepressant (TeCA) therapeuticfamily.
Purity: 99.79%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 200 mg, 500 mg
Monocrotaline N-OxideCat. No.: HY-N6828
Monocrotaline N-Oxide, a monocrotaline metabolite,leads to DNA adduct formation in vivo.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
MoxifloxacinCat. No.: HY-66011A
Moxifloxacin is a synthetic fluoroquinoloneantibiotic agent.
Purity: >98%Clinical Data: LaunchedSize: 50 mg, 100 mg, 500 mg
N-Benzylpalmitamide (N-Benzylhexadecanamide; Macamide 1) Cat. No.: HY-N2365
N-Benzylpalmitamide is a macamide isolated from, acts as an inhibitor ofLepidium meyenii
.fatty acid amide hydrolase (FAAH)
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg
www.MedChemExpress.com 25
N-Methylcytisine (Caulophylline) Cat. No.: HY-N0443
N-Methylcytisine (Caulophylline), a tricyclicquinolizidine alkaloid, exerts hypoglycaemic,analgesic and anti-inflammatory activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
N-NornuciferineCat. No.: HY-N2129
N-Nornuciferine is an aporphine alkaloid in lotusleaf that significantly inhibits with CYP2D6 IC50
and of 3.76 and 2.34 μM, respectively.Ki
Purity: 99.38%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
N-trans-Feruloyltyramine (N-feruloyltyramine; Moupinamide) Cat. No.: HY-N2410
N-trans-Feruloyltyramine (N-feruloyltyramine), analkaloid from , is an inhibitor of Piper nigru COX1and , with potential antioxidant properties.COX2N-trans-Feruloyltyramine possessesanti-inflammatory activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
N-BenzyllinolenamideCat. No.: HY-N3033
N-Benzyllinolenamide is a natural macamideisolated from , acts as anLepidium meyeniiinhibitor of fatty acid amide hydrolase ( )FAAHwith an of 41.8 μM.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
N6-Methyladenosine (6-Methyladenosine; N-Methyladenosine) Cat. No.: HY-N0086
N6-Methyladenosine is the most prevalent internal(non-cap) modification present in the messengerRNA (mRNA) of all higher eukaryotes.
Purity: 99.51%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 500 mg
Narciclasine (Lycoricidinol) Cat. No.: HY-16563
Narciclasine is a plant growth modulator.Narciclasine modulates the Rho/Rho kinase/LIMkinase/cofilin signaling pathway, greatlyincreasing GTPase RhoA activity as well asinducing actin stress fiber formation in aRhoA-dependent manner.
Purity: 99.94%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
Neferine ((-)-Neferine) Cat. No.: HY-N0441
Neferine is a major bisbenzylisoquinline alkaloid.Neferine strongly inhibits activation.NF-κB
Purity: 99.92%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
NeotuberostemonineCat. No.: HY-N3196
Neotuberostemonine, one of the main antitussivealkaloids in the root of Stemona tuberosa Lour,attenuates bleomycin-induced pulmonary fibrosis bysuppressing the recruitment and activation ofmacrophages.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
NicergolineCat. No.: HY-B0702
Nicergoline is an ergot derivative used to treatsenile dementia and other disorders with vascularorigins. Target: Alpha-1A adrenergic receptorNicergoline acts by inhibiting the postsynapticalpha(1)-adrenoceptors on vascular smooth muscle.
Purity: 99.06%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg
Nifuratel (NF 113; SAP 113; Methylmercadone) Cat. No.: HY-A0059
Nifuratel(NF 113, SAP 113) is a broadantibacterial spectrum agent, which is used as anantibacterial, antifungal, and antiprotozoal(Trichomonas).
Purity: 99.96%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
26 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
NigakinoneCat. No.: HY-N2128
Nigakinone is one of the most abundant alkaloidsresponsible for the major pharmacologicalactivities of Kumu.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
Nonivamide (Pseudocapsaicin; Pelargonic acid vanillylamide;
Nonanoic acid vanillylamide) Cat. No.: HY-17568
Nonivamide is a <b<TRPV1 agonist, whichexhibits 4d- value of 5.1 mg/L in staticEC50
toxicity tests.
Purity: 98.15%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg, 5 g
Norfloxacin hydrochloride (MK-0366 (hydrochloride)) Cat. No.: HY-B0132A
Norfloxacin (hydrochloride) (MK-0366(hydrochloride)) is a broad-spectrum antibioticthat is active against both Gram-positive andGram-negative bacteria, which functions byinhibiting DNA gyrase.
Purity: >98%Clinical Data: LaunchedSize: 5 g, 10 g
Norisoboldine ((+)-Laurelliptine) Cat. No.: HY-N0586
Norisoboldine is an isoquinoline alkaloid whichacts as an AhR agonist, and enhances the functionof the .adenosine A1 receptor
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
NuciferineCat. No.: HY-N0049
Nuciferine is an antagonist at ( =4785-HT2A IC50
nM), ( =131 nM), and ( =15-HT2C IC50 5-HT2B IC50
μM), an inverse agonist at ( =150 nM),5-HT7 IC50
a partial agonist at ( =64 nM), D2 EC50 D5
( =2.6 μM) and ( =700 nM), anEC50 5-HT6 EC50
agonist at ( =3.2 μM) and…5-HT1A EC50
Purity: 99.66%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
Orotic acid (6-Carboxyuracil; Vitamin B13) Cat. No.: HY-N0157
Orotic acid (OA) is an intermediate in pyrimidinemetabolism.
Purity: 95.75%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
Oxaceprol (N-Acetyl-L-hydroxyproline) Cat. No.: HY-17490
Oxaceprol is an anti-inflammatory drug used in thetreatment of osteoarthritis.
Purity: >95.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 g
Oxcarbazepine (GP 47680) Cat. No.: HY-B0114
Oxcarbazepine (GP 47680) inhibits the binding of[3H]BTX to sodium channels with IC of 160 μM and50
also inhibits the influx of 22Na+ into rat brainsynaptosomes with IC about 100 μM.50
Purity: 99.82%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg
Oxindole (Indolin-2-one) Cat. No.: HY-Y0061
Oxindole (Indolin-2-one) is an aromaticheterocyclic building block. 2-indolinonederivatives have become lead compounds in theresearch of kinase inhibitors.
Purity: 98.25%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Oxyberberin (Berlambine; 8-Oxoberberine; Ketoberberine) Cat. No.: HY-N5027
Berlambine is a natural alkaloid isolated frommany plants.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 27
OxymatrineCat. No.: HY-N0158
Oxymatrine, an alkaloid from the roots of Sophoraspecies, with anti-inflammatory, antifibrosis, andantitumor effects, inhibits the expression andiNOS
pathway.TGF-β/Smad
Purity: >98.0%Clinical Data: Phase 4Size: 10 mM × 1 mL, 100 mg, 200 mg, 500 mg, 1 g
p-SynephrineCat. No.: HY-113236
p-Synephrine is an organic compound, found inmultiple biofluids, such as urine and blood.
Purity: >97.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg
Palmatine chlorideCat. No.: HY-N0110
Palmatine chloride an isoquinoline alkaloid, is animportant medicinal herbal extract with diversepharmacological and biological properties.
Purity: 95.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 250 mg, 1 g
ParaxanthineCat. No.: HY-W016498
Paraxanthine, a caffeine metabolite, providesprotection against Dopaminergic cell death viastimulation of Ryanodine Receptor Channels.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg
PaxillineCat. No.: HY-N6778
Paxilline is an indole alkaloid mycotoxin from, acts as a potent BKPenicillium paxilli
channels inhibitor by an almost exclusivelyclosed-channel block mechanism.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Pefloxacin (Pefloxacinium) Cat. No.: HY-B0147
Pefloxacin is a an antibacterial agent andprevents bacterial DNA replication by inhibitingDNA gyrase (topoisomerse) Target: DNA gyrasePefloxacin is a synthetic chemotherapeutic agentused to treat severe and life-threateningbacterial infections.
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 500 mg
Peimine (Verticine; Dihydroisoimperialine) Cat. No.: HY-N0212
Peimine(Dihydroisoimperialine; Verticine) is anatural compound with good anti-inflammatoryeffects in vivo.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Peiminine (Verticinone; Raddeanine) Cat. No.: HY-N0213
Peiminine(Verticinone; Raddeanine) is a naturalcompound with anti-inflammatory activity. IC50value: Target: Peiminine and DXS significantlyreduced alveolar inflammation and pulmonaryinterstitial inflammation in rats withbleomycin-induced lung injury.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Peimisine (Ebeiensine) Cat. No.: HY-N0214
Peimisine(Ebeiensine) is a steroidal alkaloidwhich is the major biologically active componentin Bulbus Fritillariae; possess a variety oftoxicological and pharmacological effects onhumans.
Purity: 98.47%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Pemetrexed (LY231514) Cat. No.: HY-10820
Pemetrexed is a novel , the values ofantifolate Ki
the pentaglutamate of LY231514 are 1.3, 7.2, and65 nM for inhibits thymidylate synthase ( ),TSdihydrofolate reductase ( ), and glycinamideDHFRribonucleotide formyltransferase ( ),GARFTrespectively.
Purity: 99.30%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
28 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Pemetrexed disodium (LY231514 disodium) Cat. No.: HY-10820A
Pemetrexed disodium is a novel thatantifolateinhibits the folatedependent enzymes
, ,thymidylate synthase dihydrofolate reductaseand glycinamide ribonucleotide
with s of 1.3, 7.2, and 65formyltransferase Ki
nM, respectively.
Purity: 99.77%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg, 200 mg
Penitrem ACat. No.: HY-N6776
Penitrem A is an indole diterpene neurotoxicalkaloid produced by , acts as aPenicilliumselective antagonist withBK channelantiproliferative and anti-invasive activitiesagainst multiple malignancies.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Perindopril (S-9490) Cat. No.: HY-B0130
Perindopril is a long-acting ACE inhibitor ofwhich is used to treat high blood pressure, heartfailure or stable coronary artery disease. Target:ACE Perindopril is a long-acting ACE inhibitor.
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 500 mg
Pilocarpine HydrochlorideCat. No.: HY-B0726
Pilocarpine Hydrochloride is a selective M3-typemuscarinic acetylcholine receptor (M3
) agonist.muscarinic receptor
Purity: 99.92%Clinical Data: LaunchedSize: 100 mg, 500 mg
Pioglitazone (U 72107) Cat. No.: HY-13956
Pioglitazone is a potent and selective PPARγagonist with high affinity binding to the PPARγligand-binding domain with of 0.93 and 0.99EC50
μM for human and mouse PPARγ, respectively.
Purity: 99.18%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg
Piperine (Bioperine; 1-Piperoylpiperidine) Cat. No.: HY-N0144
Piperine, a natural alkaloid isolated from Piper L, inhibits and nigrum P-glycoprotein CYP3A4
activities with an value of 61.94±0.054 μg/mLIC50
in HeLa cell.
Purity: 98.76%Clinical Data: Phase 2Size: 10 mM × 1 mL, 200 mg, 1 g, 5 g
Piperlongumine (Piplartine) Cat. No.: HY-N2329
Piperlongumine is a natural alkaloid isolated from Linn, possesses ant-inflammatory,Piper longum
antibacterial, antiangiogenic, antioxidant,antitumor, and antidiabetic activities.Piperlongumine induces ROS, and induces apoptosisin cancer cell lines.
Purity: 99.19%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg
Piperlotine CCat. No.: HY-N3049
Piperlotine C is an alkaloid isolated from Piper, with anti-platelet aggregation induced bylolot
arachidonic acid, and the is 26.6 µg/mL.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Pirmenol hydrochloride (Cl-845; (±)-Pirmenol hydrochlorid) Cat. No.: HY-100795A
Pirmenol hydrochloride inhibits by blockingIK.ACh
. The of Pirmenol formuscarinic receptors IC50
inhibition of Carbachol-induced I is 0.1 μM.K.ACh
Purity: 95.63%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg, 50 mg, 100 mg
Pizotifen malate (BC-105 (malate); Pizotyline (malate)) Cat. No.: HY-B0115A
Pizotifen (malate) (BC-105 (malate)) is a potent receptor antagonist, with a high affinity5-HT2
for binding site.5-HT1C
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 200 mg, 500 mg
www.MedChemExpress.com 29
PrazosinCat. No.: HY-B0193
Prazosin is an alpha-adrenergic blocker and is asympatholytic drug used to treat high bloodpressure and anxiety, PTSD, and panic disorder.Target: Adrenergic Receptor Prazosin, is asympatholytic drug used to treat high bloodpressure and anxiety, PTSD, andpanic disorder.
Purity: >98%Clinical Data: LaunchedSize: 10 mg
Protopine (Corydinine) Cat. No.: HY-N0793
Protopine, an isoquinoline alkaloid contained inplants in northeast Asia.
Purity: 99.92%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
QuinidineCat. No.: HY-B1751
Quinidine is an antiarrhythmic agent for thetreatment of abnormal heart rhythms and alsomalaria.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Rauwolscine hydrochloride (α-Yohimbine hydrochloride;
Corynanthidine hydrochloride; Isoyohimbine hydrochloride) Cat. No.: HY-12710A
Rauwolscine hydrochloride is a potent and specific receptor antagonist with a of 12α2 adrenergic Ki
nM.
Purity: 99.95%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
ReserpineCat. No.: HY-N0480
Reserpine is an inhibitor of the vesicular ( ).monoamine transporter 2 VMAT2
Purity: 99.83%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Reserpine hydrochlorideCat. No.: HY-N0480A
Reserpine hydrochloride is an inhibitor of the ( ).vesicular monoamine transporter 2 VMAT2
Purity: 99.84%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
RhynchophyllineCat. No.: HY-N0387
Rhyncholphylline, an alkaloid isolated fromUncaria, shows potent inhibition oflipopolysaccharide (LPS)-induced NO production inrat primary microglial cells.
Purity: 99.45%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Roquinimex (Linomide; FCF89; ABR212616) Cat. No.: HY-13743
Roquinimex (Linomide; PNU212616; ABR212616) is aquinoline derivative immunostimulant whichincreases NK cell activity and macrophagecytotoxicity; inhibits angiogenesis and reducesthe secretion of TNF alpha.
Purity: 98.88%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Rotundine ((-)-Tetrahydropalmatine; L-Tetrahydropalmatine) Cat. No.: HY-N0096
Rotundine is an antagonist of , dopamine D1 D2and with s of 166 nM, 1.4 μMD3 receptors IC50
and 3.3 μM, respectively. Rotundine is also anantagonist of with an of 370 nM.5-HT1A IC50
Purity: 99.88%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg
Rubitecan (RFS 2000; 9-Nitrocamptothecin) Cat. No.: HY-13744
Rubitecan (RFS 2000), a Camptothecin derivative,is an orally active inhibitortopoisomerase Iwith broad antitumor activity, and inducesprotein-linked DNA single-strand breaks, therebyblocking DNA and RNA synthesis in dividing cells.
Purity: 98.79%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
30 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Rufinamide (CGP 33101; E 2080; RUF 331) Cat. No.: HY-A0042
Rufinamide(E 2080; CGP 33101; RUF 331) is a newantiepileptic agent that differs structurally fromother antiepileptic drugs and is approved asadjunctive therapy for Lennox-Gastaut syndrome(LGS).
Purity: 99.89%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 100 mg
Rutaecarpine (Rutecarpine) Cat. No.: HY-N0147
Rutaecarpine, an alkaloid of , isEvodia rutaecarpaan inhibitor of with an value of 0.28COX-2 IC50
μM.
Purity: 99.11%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Salsolidine (6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline) Cat. No.: HY-22385
Salsolidine is a tetrahydroisoquinoline alkaloid,acts as a stereoselective competitive MAO Ainhibitor.
Purity: 95.77%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 25 mg, 50 mg, 100 mg
Sanguinarine (Pseudochelerythrine; Sanguinarin) Cat. No.: HY-N0052
Sanguinarine, a benzophenanthridine alkaloidderived from the root of , canSanguinaria Canadensisstimulate via activating the productionapoptosisof reactive oxygen species (ROS).Sanguinarine-induced apoptosis is associated withthe activation of JNK and NF-κB.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Sanguinarine chloride (Pseudochelerythrine chloride; Sanguinarium chloride) Cat. No.: HY-N0052A
Sanguinarine chloride, a benzophenanthridinealkaloid derived from the root of Sanguinaria
, can stimulate via activatingCanadensis apoptosisthe production of reactive oxygen species (ROS).Sanguinarine-induced apoptosis is associated withthe activation of JNK and NF-κB.
Purity: 99.80%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Santacruzamate A (CAY-10683) Cat. No.: HY-N0931
Santacruzamate A (CAY-10683) is a potent andselective inhibitor with an of 119 pM.HDAC2 IC50
Purity: 99.72%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Sapropterin dihydrochloride (6R-BH4 dihydrochloride;
6R-Tetrahydro-L-biopterin dihydrochloride) Cat. No.: HY-A0124A
Sapropterin dihydrochloride is a synthetic form ofBH4 that is approved for the treatment of BH4responsive PKU.
Purity: 99.97%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Sauristolactam (Saurolactam) Cat. No.: HY-118482
Sauristolactam, a natural aristolactam isolatedfrom aerial portions of , hasSaururus chinensissignificant neuroprotective activity againstglutamate-induced toxicity in primary cultured ratcortical cells.
Purity: >98%Clinical Data: No Development ReportedSize: 250 mg, 500 mg
SchinifolineCat. No.: HY-N4164
Schinifoline, a 4-quinolinone derivative isolatedfrom Sieb, improvesZanthoxylum schinifoliumradiosensitizing effect, and effects cell cycleand apoptotic-inducing effects in cancer .
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Scopine (6,7-Epoxytropine) Cat. No.: HY-B0459
Scopine is the metabolite of anisodine, which is aα1-adrenergic receptor agonist and used in thetreatment of acute circulatory shock.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg, 50 mg, 100 mg
www.MedChemExpress.com 31
Scopolamine (Hyoscine; Scopine (-)-tropate; Scopine tropate) Cat. No.: HY-N0296
Scopolamine is a high affinity (nM) muscarinicantagonist. receptor-responses are5-HT3
reversibly inhibited by Scopolamine with an IC50
of 2.09 μM.
Purity: >98%Clinical Data: LaunchedSize: 100 mg
Scopolamine butylbromide (Hyoscine butylbromide;
(-)-Scopolamine butylbromide; Butylscopolamine bromide) Cat. No.: HY-N0340
Scopolamine butylbromide is a competitiveantagonist of muscarinic acetylcholine receptor(mAChR) with an IC50 of 55.3 ± 4.3 nM.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
Scopolamine hydrobromide ((-)-Scopolamine hydrobromide;
Hyoscine hydrobromide; Scopine hydrobromide) Cat. No.: HY-N0296A
Scopolamine hydrobromide is a high affinity (nM) antagonist. muscarinic 5-HT3
receptor-responses are reversibly inhibited byScopolamine with an of 2.09 μM.IC50
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
Senecionine (Senecionan-11,16-dione, 12-hydroxy-; Aureine; Senecionin) Cat. No.: HY-N2560
Senecionine is a pyrrolizidine alkaloid isolatedfrom . Senecionine is toxic toSenecio vulgarisanimals and humans.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
SeneciphyllinineCat. No.: HY-N1283
Seneciphyllinine, a pyrrolizidine alkaloid, isisolated from the roots of .Gynura japonicaPyrrolizidine alkaloids are highly hepatotoxicnatural chemicals that produce irreversiblechronic and acute hepatotoxic effects on humanbeings.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Setiptiline maleate (MO-8282) Cat. No.: HY-32329A
Setiptiline is a serotonin receptor antagonist.
Purity: 99.89%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg, 200 mg
SinapineCat. No.: HY-N5077
Sinapine is an alkaloid from seeds of thecruciferous species which shows favorablebiological activities such as antioxidant andradio-protective activities.
Purity: 99.72%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Sinapine thiocyanateCat. No.: HY-N0450
Sinapine thiocyanate is an alkaloid from seeds ofthe cruciferous species which shows favorablebiological activities such as antioxidant andradio-protective activities.
Purity: 98.32%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg
Sinomenine hydrochloride (Cucoline hydrochloride) Cat. No.: HY-15122A
Sinomenine hydrochloride is a blocker of the activation and also an activator of NF-κB μ-opioid
.receptor
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Sipeimine (Imperialine) Cat. No.: HY-N0696
Sipeimine is a natural product isolated fromFritillaria ussuriensis.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
32 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
Solamargine (Solamargin; δ-Solanigrine) Cat. No.: HY-N0069
Solamargine is a major steroidal alkaloidglycoside extracted from a traditional Chinesemedicinal herb, Solanum nigrum L. (SNL); has beenshown to inhibit growth and induce apoptosis ofvarious cancer cells.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Solasodine (Purapuridine; Solancarpidine; Solasodin) Cat. No.: HY-N0068
Solasodine(Purapuridine) is a poisonous alkaloidchemical compound that occurs in plants of theSolanaceae family. Solasodine showed selectivecytotoxicity against cervical cancer cell line(HeLa) and human myeloid leukemia cell line(U937).
Purity: >98.0%Clinical Data: No Development ReportedSize: 100 mg
SophocarpineCat. No.: HY-N0103
Sophocarpine is one of the significant alkaloidextracted from the traditional herb medicine
which has many pharmacologicalSophora flavescensproperties such as anti-virus, anti-tumor,anti-inflammatory.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Sophocarpine (monohydrate)Cat. No.: HY-N0103A
Sophocarpine (monohydrate) is one of thesignificant alkaloid extracted from thetraditional herb medicine whichSophora flavescenshas many pharmacological properties such asanti-virus, anti-tumor, anti-inflammatory.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Stachydrine hydrochlorideCat. No.: HY-N0738
Stachydrine hydrochloride is the major activeconstituent of , which is a potentialHerba Leonuritherapy for cardiovascular diseases. Stachydrinecan inhibit the signal pathway.NF-κBAnti-hypertrophic activities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Staurosporine (Antibiotic AM-2282; STS; AM-2282) Cat. No.: HY-15141
Staurosporine is a potent and non-selectiveinhibitor of protein kinases with s of 6 nM,IC50
15 nM, 2 nM, and 3 nM for , , , andPKC PKA c-Fgr respectively.Phosphorylase kinase
Purity: 99.98%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 2 mg, 5 mg, 10 mg
SulfapyridineCat. No.: HY-B0212
Sulfapyridine(Dagenan) is a sulfonamideantibacterial.
Purity: 99.96%Clinical Data: LaunchedSize: 1 g, 5 g
SulfathiazoleCat. No.: HY-B0507
Sulfathiazole is an organosulfur compound that hasbeen used as a short-acting sulfa drug. Target:Antibacterial Sulfathiazole (20 μg/L) starts to bedegraded between day 31 and day 38 in one of thetwo batch reactors containing different wastewatermatrices.
Purity: >98%Clinical Data: LaunchedSize: 1 g
Swainsonine (Tridolgosir) Cat. No.: HY-N6722
Swainsonine is an alkaloid isolated from, acts as an inhibitor ofAstragalus
, with anti-tumor activity.α-mannosidase
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Synephrine hydrochloride (Oxedrine hydrochloride) Cat. No.: HY-N0132A
Synephrine hydrochloride (Oxedrine hydrochloride)is an alkaloid. Synephrine hydrochloride (Oxedrinehydrochloride) produces most of its biologicaleffects by acting as an agonist at adrenergicreceptors.
Purity: 99.83%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 500 mg
www.MedChemExpress.com 33
Talipexole (B-HT 920) Cat. No.: HY-A0040
Talipexole (B-HT920) is a dopamine agonist thathas been proposed as an antiparkinsonian agent.Target: Dopamine Receptor B-HT920 is a selectivealpha 2-adrenoceptor agonist.
Purity: >98%Clinical Data: LaunchedSize: 5 mg, 10 mg, 50 mg, 100 mg
Tandospirone citrate (SM-3997 citrate) Cat. No.: HY-B0061
Tandospirone citrate is a potent and selective5-HT1A receptor partial agonist (Ki = 27 nM) thatdisplays selectivity over SR-2, SR-1C, α1, α2, D1and D2 receptors (Ki values ranging from1300-41000 nM).
Purity: 98.87%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
TerazosinCat. No.: HY-B0371
Terazosin is a selective alpha1-antagonist usedfor treatment of symptoms of benign prostatichyperplasia (BPH).
Purity: >98%Clinical Data: LaunchedSize: 100 mg, 500 mg
Tetrahydroberberine (Canadine) Cat. No.: HY-N0925
Tetrahydroberberine is an isoquinoline alkaloidisolated from corydalis tuber; has micromolaraffinity for dopamine D(2) (pK(i) = 6.08) and5-HT(1A) (pK(i) = 5.38) receptors but moderate tono affinity for other relevant serotonin receptors(5-HT(1B), 5-HT(1D), 5-HT(3), and 5-HT(4);…
Purity: 99.70%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Tetrahydrocoptisine ((RS)-Stylopine; (±)-Stylopin) Cat. No.: HY-N0924
Tetrahydrocoptisine is an alkaloid compoundoriginally isolated from Corydalis tubers thatexhibits anti-inflammatory and anti-parasiticactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Tetrahydropalmatine (DL-Tetrahydropalmatine) Cat. No.: HY-N0300
Tetrahydropalmatine, an active component isolatedfrom corydalis, acts through inhibition ofamygdaloid release of to inhibit andopamineepileptic attack in rats.
Purity: 99.07%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Tetramethylpyrazine (Ligustrazine) Cat. No.: HY-N0264
Tetramethylpyrazine (Ligustrazine), analkylpyrazine isolated from Ligusticum
( ), is present in frenchwallichii Chuan Xiongfries, bread, cooked meats, tea, cocoa, coffee,beer, spirits, peanuts, filberts, dairy productsand soy products as fragrance and…
Purity: 99.93%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Theobromine (3,7-Dimethylxanthine) Cat. No.: HY-N0138
Theobromine is a methylxanthine found in cacaobeans which can inhibit adenosine receptor A1( ) signaling.AR1
Purity: 99.65%Clinical Data: Phase 3Size: 10 mM × 1 mL, 100 mg
Theophylline (1,3-Dimethylxanthine; Theo-24) Cat. No.: HY-B0809
Theophylline is a nonselective phosphodiesterase inhibitor, blocker, and(PDE) adenosine receptor
activator.histone deacetylase (HDAC)
Purity: 99.94%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 g
Thymidine (DThyd; Deoxyribothymidine; Deoxythymidine; NSC
21548; Thymidin) Cat. No.: HY-N1150
Thymidine is a a pyrimidine deoxynucleoside.
Purity: 99.90%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 g
34 Tel: 609-228-6898 Fax: 609-228-5909 Email: sales@MedChemExpress.com
ThymineCat. No.: HY-W010450
Thymine is one of the four nucleobases in thenucleic acid of DNA and can be a target foractions of 5-fluorouracil (5-FU) in cancertreatment, with a K of 2.3 μM.m
Purity: 99.98%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 g
Tiagabine (NO050328; NO328; TGB) Cat. No.: HY-B0696
Tiagabine (NO050328) is a potent and selective inhibitor, used as anGABA reuptake
anticonvulsant agent, with s of 67, 446 andIC50
182 nM for [ H]GABA uptake in Synaptosomes,3
Neurons and Glia, respectively.
Purity: >98%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg
Tigecycline (GAR-936) Cat. No.: HY-B0117
Tigecycline (GAR-936) is a broad-spectrumglycylcycline antibiotic. The mean inhibitoryconcentration (MIC) of Tigecycline for E. coli(MG1655 strain) is approximately 125 ng/mL.
Purity: 99.88%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg, 200 mg, 500 mg
TomatidineCat. No.: HY-N2149
Tomatidine acts as an anti-inflammatory agent byblocking and signaling.NF-κB JNK
Purity: >98.0%Clinical Data: No Development ReportedSize: 25 mg, 50 mg, 100 mg
Tomatine (α-Tomatine; Lycopersicin; Tomatin) Cat. No.: HY-N2166
Tomatine is a glycoalkaloid, found in the tomatoplant ( Mill.). TomatineLycopersicon esculentumelicits neurotoxicity in RIP1 kinase andcaspase-independent manner. Tomatine promotes theupregulation of nuclear apoptosis inducing factor(AIF) in neuroblastoma cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Trabectedin (Ecteinascidin 743; ET-743) Cat. No.: HY-50936
Trabectedin (Ecteinascidin-743 or ET-743) is anovel antitumour agent of marine origin withpotent antitumour activity both in vitro and invivo.
Purity: 99.83%Clinical Data: LaunchedSize: 1 mg
Trigonelline (Trigenolline) Cat. No.: HY-N0414
Trigonelline, an alkaloid with potentialantidiabetic activity, is present in considerableamounts in coffee.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
Trigonelline chloride (Trigonelline hydrochloride) Cat. No.: HY-N0415
Trigonelline chloride, an alkaloid with potentialantidiabetic activity, is present in considerableamounts in coffee.
Purity: 99.96%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 500 mg
Tropisetron (SDZ-ICS-930 (free base)) Cat. No.: HY-B0072
Tropisetron (SDZ-ICS-930 free base) is a selective5-HT3 receptor antagonist and α7-nicotinicreceptor agonist with an IC50 of 70.1 ± 0.9 nM for5-HT3 receptor.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
TryptamineCat. No.: HY-B2132
Tryptamine is a monoamine alkaloid, similar toother trace amines, is believed to play a role asa neuromodulator or neurotransmitter.
Purity: 99.77%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg
www.MedChemExpress.com 35
Veratramine (NSC17821; NSC23880) Cat. No.: HY-N0837
Veratramine(NSC17821; NSC23880) is useful as asignal transduction inhibitor for treating tumors.
Purity: 99.52%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
VicineCat. No.: HY-N2093
Vicine, an alkaloid glycoside found mainly in favabeans, is toxic in individuals and may causehaemolytic anaemia.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Vinblastine sulfate (Vincaleukoblastine sulfate salt) Cat. No.: HY-13780
Vinblastine sulfate is a cytotoxic alkaloid usedagainst various cancer types. Vinblastine sulfateinhibits the formation of microtubule andsuppresses nAChR with an of 8.9 μM.IC50
Purity: 99.85%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
VincamineCat. No.: HY-B1021
Vincamine is a peripheral vasodilator, thatincreases blood flow to the brain.
Purity: 99.93%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
Vincristine sulfate (Leurocristine sulfate; 22-Oxovincaleukoblastine sulfate) Cat. No.: HY-N0488
Vincristine sulfate is an antitumor vinca alkaloidwhich inhibits formation in mitoticmicrotubulespindle, resulting in an arrest of dividing cellsat the metaphase stage. It binds to microtubulewith a of 85 nM.Ki
Purity: 99.66%Clinical Data: LaunchedSize: 10 mg, 50 mg, 100 mg, 200 mg
VinflunineCat. No.: HY-B0628
Vinflunine is a new vinca alkaloid uniquelyfluorinated with the properties ofmitotic-arresting and tubulin-interactingactivity.
Purity: >98%Clinical Data: LaunchedSize: 5 mg, 10 mg, 50 mg, 100 mg
WilforineCat. No.: HY-N0899
Wilforine is a sesquiterpene pyridine alkaloid;important bioactive compound in T. wilfordiiplants, and is effective in treating idiopathicpulmonary fibrosis.
Purity: 98.30%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Yohimbine HydrochlorideCat. No.: HY-N0127
Yohimbine Hydrochloride is an alpha2-adrenoreceptor antagonist, blocking the pre- andpostsynaptic alpha-2 adrenoreceptors and causingan increased release of noradrenaline anddopamine.
Purity: 99.85%Clinical Data: Phase 4Size: 10 mM × 1 mL, 1 g
Yunaconitine (Guayewuanine B) Cat. No.: HY-N0333
Yunaconitine(Guayewuanine B) is a highly toxicaconitum alkaloid.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
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