Rational design of potent carboxylic acid based bisubstrate inhibitors of ras farnesyl protein transferase-Reference-Cited by-同舟云学术

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Rational design of potent carboxylic acid based bisubstrate inhibitors of ras farnesyl protein transferase

Published:1994-09 Issue:17 Volume:4 Page:2107-2112
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Bhide Rajeev S.,Patel Dinesh V.,Patel Manorama M.,Robinson Simon P.,Hunihan Lisa W.,Gordon Eric M.

Publisher

Elsevier BV

Subject

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

Reference12 articles.

2. Tetrapeptide inhibitors of protein farnesyltransferase: amino-terminal substitution in phenylalanine-containing tetrapeptides restores farnesylation.

3. Selective Inhibition of ras -Dependent Transformation by a Farnesyltransferase Inhibitor

4. Benzodiazepine Peptidomimetics: Potent Inhibitors of Ras Farnesylation In Animal Cells

5. Potent inhibition of human tumor p21ras farnesyltransferase by A1A2-lacking p21ras CA1A2X peptidomimetics.

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2. Highly regio- and chemoselective palladium(0)-mediated allylic substitution of difunctional allylic halides with phenols;Tetrahedron Letters;2010-12

3. Towards the synthesis of bisubstrate inhibitors of protein farnesyltransferase: Synthesis and biological evaluation of new farnesylpyrophosphate analogues;Bioorganic & Medicinal Chemistry;2010-01

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