4.5 Article

Penicacids A-C, three new mycophenolic acid derivatives and immunosuppressive activities from the marine-derived fungus Penicillium sp SOF07

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 22, 期 9, 页码 3332-3335

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2012.02.106

关键词

Marine fungi; Penicillium sp.; Penicacid A-C; Inosine-monophosphate dehydrogenase; Structure-activity relationship

资金

  1. Chinese Academy of Sciences [KZCX2-YW-JC202, KZCX2-EW-G-12, KSCX2-YW-G-065, 08SL111001]
  2. '863' Project [2012AA092104]
  3. Science and Technology Planning Project of Guangdong Province [2010B030600010]
  4. Scientific Research Foundation for the Returned Overseas Chinese Scholars of the State Education Ministry

向作者/读者索取更多资源

Three new mycophenolic acid derivatives, penicacids A-C (1-3), together with two known analogues, mycophenolic acid (MPA, 4) and 4'-hydroxy-MPA (5), were isolated from a fungus Penicillium sp. SOF07 derived from a South China Sea marine sediment. The structures of compounds 1-3 were elucidated on the basis of MS and NMR (H-1, C-13, HSQC and HMBC) data analyses and comparisons with the known compounds. Structure-activity relationship studies of compounds 1-5 focused on inosine-monophosphate dehydrogenase inhibition revealed that hydroxylation at C-4', methylation at C-7-OH, dual hydroxylation at C-2'/C-3' double bond of MPA diminished bioactivity whereas glucosyl hydroxylation at C-4' correlated to bioactivity comparable to that observed for MPA. (C) 2012 Elsevier Ltd. All rights reserved.

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