Calbistrin E and two other new metabolites from an Australian isolate of Penicillium striatisporum


Autoria(s): Stewart, M.; Capon, R. J.; Lacey, E.; Tennant, S.; Gill, J. H.
Data(s)

01/01/2005

Resumo

An Australian isolate of Penicillium striatisporum collected near Shalvey, New South Wales, exhibited selective antifungal activity against Candida albicans versus Saccharomyces cerevisiae. Bioassay-directed fractionation yielded members of the rare class of fungal metabolites known as the calbistrins. These included a new example of this structure class, calbistrin E (1), as well as the known polyenes calbistrin C (2) and deformylcalbistrin A (3). Also recovered from P. striatisporum were new triene and butenolide acids, striatisporin A (4) and striatisporolide A (5), together with the known fungal metabolites versiol (6) and (+)-hexylitaconic acid (7). Structures for all metabolites were determined by detailed spectroscopic analysis.

Identificador

http://espace.library.uq.edu.au/view/UQ:76075

Idioma(s)

eng

Publicador

Amer Chemical Soc

Palavras-Chave #Plant Sciences #Chemistry, Applied #Chemistry, Medicinal #Pharmacology & Pharmacy #Fungal Metabolite #Antifungal Agent #Restrictum #Elucidation #C1 #250300 Organic Chemistry #780103 Chemical sciences #030401 Biologically Active Molecules #030502 Natural Products Chemistry
Tipo

Journal Article