Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
ECB-ART-40349
Bioorg Med Chem 2007 Nov 01;1521:6687-91. doi: 10.1016/j.bmc.2007.08.011.
Show Gene links Show Anatomy links

Bioassay-guided fractionation of pterocarpans from roots of Harpalyce brasiliana Benth.

Militão GC , Pinheiro SM , Dantas IN , Pessoa C , de Moraes MO , Costa-Lotufo LC , Lima MA , Silveira ER .


???displayArticle.abstract???
Pterocarpans, a special kind of isoflavonoids possessing two contiguous benzofuran and benzopyran rings, have been reported as possessing several biological activities. In order to isolate and identify the active principles possibly responsible for the stronger activity of the EtOH extract from roots of Harpalyce brasiliana on the antimitotic assay using sea urchin egg development, a bioassay-guided fractionation was performed. Six bioactive pterocarpan derivatives: 4''-dehydroxycabenegrin A-I, leiocarpin, medicarpin, cabenegrins A-I and A-II, and maackiain were isolated from the chloroform fraction of H. brasiliana extract. Leiocarpin was the most active on the sea urchin egg assay with IC(50) values ranging from 0.1 to 1.2 microg/mL, followed by 4''-dehydroxycabenegrin A-I. The isolated compounds were also tested for cytotoxicity against tumor cell lines in cultures, where 4''-dehydroxycabenegrin A-I was the most active, followed by leiocarpin. Additionally, some studies on the structure-activity relationship of these pterocarpans are suggested.

???displayArticle.pubmedLink??? 17764956
???displayArticle.link??? Bioorg Med Chem


Genes referenced: LOC100887844 LOC100893907 LOC115919910