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Thiersindoles A-C: new indole diterpenoids from Penicillium thiersii
Journal article   Peer reviewed

Thiersindoles A-C: new indole diterpenoids from Penicillium thiersii

Chen Li, James B Gloer and Donald T Wicklow
Journal of natural products (Washington, D.C.), Vol.66(9), pp.1232-1235
09/2003
DOI: 10.1021/np030192m
PMID: 14510604

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Abstract

Three new 3-substituted indole diterpenoids (thiersindoles A-C; 1-3) have been isolated from organic extracts of a new Penicillium species (P. thiersii). Their structures, including absolute stereochemistry, were determined by analysis of NMR data and application of Mosher's method. Thiersindoles A-C are biogenetically related to the aflavinines, although the [6,6,5] tricyclic diterpenoid skeleton in compounds 1 and 2 is unprecedented in any of the known members of this class.
Animals Diterpenes - chemistry Diterpenes - isolation & purification Diterpenes - pharmacology Indoles - chemistry Indoles - isolation & purification Indoles - pharmacology Molecular Structure Nuclear Magnetic Resonance, Biomolecular Penicillium - chemistry Stereoisomerism

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