Chemical modifications of natural triterpenes—glycyrrhetinic and boswellic acids: evaluation of their biological activity


Autoria(s): Rao, GSR Subba; Kondaiah, Paturu; Singh, Sanjay K; Ravanan, Palaniyandi; Sporn, Michael B
Data(s)

15/12/2008

Resumo

Synthetic analogues of naturally occurring triterpenoids; glycyrrhetinic acid, arjunolic acid, and boswellic acids, by modification of A-ring with a cyano- and enone-functionality, have been reported. A novel method of synthesis of α-cyanoenones from isoxazoles is reported. Bioassays using primary mouse macrophages and tumor cell lines indicate potent anti-inflammatory and cytotoxic activities associated with cyano-enones of boswellic acid and glycyrrhetinic acid.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/26056/1/http___www.sciencedirect.com_science__ob%3DMImg%26_imagekey%3DB6THR-4TPPDX1-1-F%26_cdi%3D5289%26_.pdf

Rao, GSR Subba and Kondaiah, Paturu and Singh, Sanjay K and Ravanan, Palaniyandi and Sporn, Michael B (2008) Chemical modifications of natural triterpenes—glycyrrhetinic and boswellic acids: evaluation of their biological activity. In: Tetrahedron Letters, 64 (51). pp. 11541-11548.

Publicador

Elsevier Science

Relação

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6THR-4TPPDX1-1&_user=512776&_coverDate=12%2F15%2F2008&_rdoc=1&_fmt=high&_orig=search&_sort=d&_docanchor=&view=c&_searchStrId=1240076531&_rerunOrigin=google&_acct=C000025298&_version=1&_urlVersion=0

http://eprints.iisc.ernet.in/26056/

Palavras-Chave #Molecular Reproduction, Development & Genetics (formed by the merger of DBGL and CRBME) #Organic Chemistry
Tipo

Journal Article

PeerReviewed