Farnesoid X-activated receptor antagonists from a marine sponge Spongia sp.
Sang-Jip Nam, Hyunsil Ko, Mihee Shin, Jungyeob Ham, Jungwook Chin, Youngshin Kim, Heeyoung Kim, Kyoungjin Shin, Hyukjae Choi, Heonjoong Kang
Index: Bioorg. Med. Chem. Lett. 16 , 5398-402, (2006)
Full Text: HTML
Abstract
Three novel (1-3) and two known (4-5) scalarane sesterterpenes were isolated from a marine sponge of the genus Spongia. The isolated compounds showed potent inhibition of transactivation for the nuclear hormone receptor, FXR (farnesoid X-activated receptor), which is a promising drug target to treat hypercholesterolemia in humans.
Related Compounds
Related Articles:
Chemical genetics reveals a complex functional ground state of neural stem cells.
2007-05-01
[Nat. Chem. Biol. 3(5) , 268-273, (2007)]
Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.
2009-10-01
[Nat. Chem. Biol. 5 , 765-71, (2009)]
2014-09-01
[Biochim. Biophys. Acta 1844(9) , 1684-93, (2014)]
2009-01-01
[J. Nat. Prod. 72 , 24-8, (2009)]
Design, synthesis, and evaluation of non-steroidal farnesoid X receptor (FXR) antagonist.
2007-04-01
[Bioorg. Med. Chem. 15 , 2587-600, (2007)]