4.2 Article

Six new ergosterols from the marine-derived fungus Rhizopus sp.

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STEROIDS
卷 73, 期 1, 页码 19-26

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.steroids.2007.08.008

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sterols; marine-derived; fungi; structure identification; cytotoxicity

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Six new ergosterols, including 3 beta-hydroxyl-(22E, 24R)-ergosta-5,8,22-trien-7,15-dione (1), 3 beta-hydroxyl-(22E, 24R) -ergosta-5,8,14,22-tetraen-7-one (2), 3 beta,15 beta-dihydroxyl-(22E, 24R)-ergosta-5,8(14),22-trien-7-one (3), 3 beta,15 alpha-dihydroxyl-(22E, 24R)-ergosta-5,8(14),22-trien-7-one (4), 3 beta-hydroxyl-(22E, 24R)-ergosta-5,8(14),22-trien-7,15-dione (5), and 5 alpha,8 alpha-epidioxy-23,24(R)-dimethylcholesta-6,9(11),22-trien-3 beta-ol (6), have been isolated from the marine-derived fungus Rhizopus sp., along with four known ones (7-10). The structures of the new compounds were determined on the basis of extensive spectroscopic data. All compounds were evaluated for their cytotoxic activities on P388, A549, HL-60, and BEL-7420 cell lines by the MTT and SRB methods. (C) 2007 Published by Elsevier Inc.

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