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A screen for inhibitors of DNA recombination: identification of two new spirostanol glycosides from Chamaedorea linearis.

作者信息

Patil A D, Baures P W, Eggleston D S, Faucette L, Hemling M E, Westley J W, Johnson R K

机构信息

Department of Biomolecular Discovery, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406-0939.

出版信息

J Nat Prod. 1993 Sep;56(9):1451-8. doi: 10.1021/np50099a003.

Abstract

Two new glycosides have been isolated from the MeOH extract of the stem wood and stem bark of an Ecuadorian plant Chamaedorea linearis, and their structures have been determined by spectroscopic means and X-ray analysis of the aglycone to be 1-O-[beta-L-fucopyranosyl-(4'-sulfate)]-25R,5 alpha-spirostane-1 beta, 3 beta-diol [1]) and 1-O-[beta-L-fucopyranosyl-(4'-sulfate)]-25R,5 alpha-spirostane-1 alpha, 3 beta-diol [2]. These compounds were identified in a screen for inhibitors of recombinational DNA repair. Cytotoxic activity was also demonstrated.

摘要

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