Aryl tetrahydropyridine inhibitors of farnesyltransferase: bioavailable analogues with improved cellular potency-Reference-Cited by-同舟云学术

Aryl tetrahydropyridine inhibitors of farnesyltransferase: bioavailable analogues with improved cellular potency

Published:2003-04 Issue:7 Volume:13 Page:1363-1366
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Gwaltney Stephen L.,O'Connor Stephen J.,Nelson Lissa T.J.,Sullivan Gerard M.,Imade Hovis,Wang Weibo,Hasvold Lisa,Li Qun,Cohen Jerome,Gu Wen-Zhen,Tahir Stephen K.,Bauch Joy,Marsh Kennan,Ng Shi-Chung,Frost David J.,Zhang Haiying,Muchmore Steve,Jakob Clarissa G.,Stoll Vincent,Hutchins Charles,Rosenberg Saul H.,Sham Hing L.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference4 articles.

1. A Non-peptide Mimetic of Ras-CAAX: Selective Inhibition of Farnesyltransferase and Ras Processing

2. Design and in Vivo Analysis of Potent Non-Thiol Inhibitors of Farnesyl Protein Transferase

3. Novel small renin inhibitors containing 4,5- or 3,5-dihydroxy-2-substituted-6-phenylhexanamide replacements at the P2P3 sites

4. World Patent WO 01/81316;Wang;Chem. Abstr.,2001

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