
Phytochemistry p. 579 - 592 (1992)
Update date:2022-08-05
Topics:
Asakawa, Yoshinori
Hashimoto, Toshihiro
Mizuno, Yasuo
Tori, Motoo
Fukazawa, Yoshimasa
Seven novel bitter drimane-type sesquiterpenoids with an isocitric acid group named cryptoporic acids (CA) A-G have been isolated from the fungus Cryptoporus volvatus and their absolute stereostructures established by a combination of chemical transformation, NMR spectral data and X-ray crystallographic analysis.Crytoporic acids strongly inhibited the release of superoxide anion radicals from guinea-pig peritoneal macrophage as well as rabbit polymorphonuclear leucocyte.CA-E showed anti-tumour promoting activity whilst CA-D slightly enhanced tumour promoting and protein kinase C activity.CAs also inhibited elongation of the second coleoptile and germination of rice in husk at 200 ppm. Key words: Cryptoporus volvatus; Polyporaceae; fungus; drimane-type sesquiterpenoid ethers; isocitric acid; superoxide anion radical release inhibitor; anti-tumour and tumour promoting activity; protein kinase C enhancement; plant growth inhibitory activity; bitter principles.
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Doi:10.1002/chem.201201317
(2012)Doi:10.1039/P29920000201
(1992)Doi:10.1016/0957-4166(95)00159-M
(1995)Doi:10.1021/jo301872n
(2013)Doi:10.1246/bcsj.65.846
(1992)Doi:10.1134/S1070428014100121
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