| Literature DB >> 18321704 |
Michelle Maynor1, Sarah A Scott, Emily L Rickert, Richard A Gibbs.
Abstract
Protein prenyl transferases have been a focus of anti-cancer drug discovery in recent years due to their roles in post-translational modification of small GTP binding proteins. Attention is now turning to the development of GGTase I inhibitors. Here, we present the synthesis and biological evaluation of four GGPP analogs versus mammalian GGTase I and the discovery that 7-allyl GGPP is a surprisingly efficient GGTase I substrate.Entities:
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Year: 2008 PMID: 18321704 PMCID: PMC2376209 DOI: 10.1016/j.bmcl.2008.02.014
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823