ChemInform Abstract: Chemistry of Renieramycins. Part 10. Structure of Renieramycin V, a Novel...

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ChemInform 2012, 43, issue 17 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Alkaloids U 0600 DOI: 10.1002/chin.201217203 Chemistry of Renieramycins. Part 10. Structure of Renieramycin V, a Novel Renieramycin Marine Natural Product Having a Sterol Ether at C-14 Position. — Renieramycin V (I) is isolated from the low polar fraction obtained from the Thai blue sponge Xestospongia sp. Surprisingly (I) shows no cytotoxicity to several human cancer cell lines. — (SAITO*, N.; YOSHINO, M.; CHARUPANT, K.; SUWANBORIRUX, K.; Heterocycles 84 (2012) 1, 309-314, http://dx.doi.org/10.3987/com-11-s(p)28 ; Grad. Sch. Pharm. Sci., Meiji Pharm. Univ., Kiyose, Tokyo 204, Japan; Eng.) — M. Bohle 17- 203

Transcript of ChemInform Abstract: Chemistry of Renieramycins. Part 10. Structure of Renieramycin V, a Novel...

Page 1: ChemInform Abstract: Chemistry of Renieramycins. Part 10. Structure of Renieramycin V, a Novel Renieramycin Marine Natural Product Having a Sterol Ether at C-14 Position.

AlkaloidsU 0600 DOI: 10.1002/chin.201217203

Chemistry of Renieramycins. Part 10. Structure of Renieramycin V, a Novel Renieramycin Marine Natural Product Having a Sterol Ether at C-14 Position. — Renieramycin V (I) is isolated from the low polar fraction obtained from the Thai blue sponge Xestospongia sp. Surprisingly (I) shows no cytotoxicity to several human cancer cell lines. — (SAITO*, N.; YOSHINO, M.; CHARUPANT, K.; SUWANBORIRUX, K.; Heterocycles 84 (2012) 1, 309-314, http://dx.doi.org/10.3987/com-11-s(p)28 ; Grad. Sch. Pharm. Sci., Meiji Pharm. Univ., Kiyose, Tokyo 204, Japan; Eng.) — M. Bohle

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ChemInform 2012, 43, issue 17 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

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Sterol Metabolism - bioone.org · sterol composition of brassicaceae to which Arabidopsis belongs, presents a small difference to most plant species for an additional sterol, brassicasterol

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