Cytotoxic biflavonoids from Selaginella willdenowii
作者:Gloria L. Silva、Heebyung Chai、Mahabir P. Gupta、Norman R. Farnsworth、Geoffrey A. Cordell、John M. Pezzuto、Christopher W.W. Beecher、A. Douglas Kinghorn
DOI:10.1016/0031-9422(95)00212-p
日期:1995.9
Bioactivity-guided fractionation of the leaves of Selaginella willdenowii afforded three known biflavones, 4',7''-di-O-methylamentoflavone, isocryptomerin and 7''-O-methylrobustaflavone, that were significantly cytotoxic against a panel of human cancer cell lines. Non-cytotoxic isolates were also obtained, namely, amentoflavone, bilobetin, robustaflavone and 2'',3''-dihydroisocryptomerin, a new dihydrobiflavone. The structure for the new biflavonoid was unambiguously assigned by a combination of spectroscopic methods.
RECA INHIBITORS WITH ANTIBIOTIC ACTIVITY, COMPOSITIONS AND METHODS OF USE
申请人:Cottarel Guillaume
公开号:US20100029597A1
公开(公告)日:2010-02-04
The present invention is directed to the use of RecA inhibitors as antibiotic agents, and provides RecA inhibitors useful in treating infections. Also provided are various compositions and methods associated with RecA inhibition.
US9155792B2
申请人:——
公开号:US9155792B2
公开(公告)日:2015-10-13
Ansari, F. R.; Ansari, W. H.; Rahman, W., Journal of the Indian Chemical Society, 1985, vol. 62, # 5, p. 406 - 408