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PMID: 18020435 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

4,5-diarylisoxazole Hsp90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer.

Journal of medicinal chemistry ·Vol. 51 ·No. 2 ·2008-01-24 ·Pages 196-218

Brough PA, Aherne W, Barril X, Borgognoni J, Boxall K, Cansfield JE, Cheung KM, Collins I, Davies NG, Drysdale MJ, Dymock B, Eccles SA, Finch H, Fink A, Hayes A, Howes R, Hubbard RE, James K, Jordan AM, Lockie A, Martins V, Massey A, Matthews TP, McDonald E, Northfield CJ, Pearl LH, Prodromou C, Ray S, Raynaud FI, Roughley SD, Sharp SY, Surgenor A, Walmsley DL, Webb P, Wood M, Workman P, Wright L

Abstract

Inhibitors of the Hsp90 molecular chaperone are showing considerable promise as potential chemotherapeutic agents for cancer. Here, we describe the structure-based design, synthesis, structure-activity relationships and pharmacokinetics of potent small-molecule inhibitors of Hsp90 based on the 4,5-diarylisoxazole scaffold. Analogues from this series have high affinity for Hsp90, as measured in a fluorescence polarization (FP) competitive binding assay, and are active in cancer cell lines where they inhibit proliferation and exhibit a characteristic profile of depletion of oncogenic proteins and concomitant elevation of Hsp72. Compound 40f (VER-52296/NVP-AUY922) is potent in the Hsp90 FP binding assay (IC50 = 21 nM) and inhibits proliferation of various human cancer cell lines in vitro, with GI50 averaging 9 nM. Compound 40f is retained in tumors in vivo when administered i.p., as evaluated by cassette dosing in tumor-bearing mice. In a human colon cancer xenograft model, 40f inhibits tumor growth by approximately 50%.

MeSH Terms
Animals Antineoplastic Agents/chemical synthesis,pharmacokinetics,pharmacology Binding, Competitive Cell Line, Tumor Cell Proliferation/drug effects Crystallography, X-Ray Drug Screening Assays, Antitumor Fluorescence Polarization HSP90 Heat-Shock Proteins/antagonists & inhibitors,metabolism Humans Isoxazoles/chemical synthesis,pharmacokinetics,pharmacology Mice Mice, Nude Models, Molecular Neoplasm Transplantation Resorcinols/chemical synthesis,pharmacokinetics,pharmacology Structure-Activity Relationship Transplantation, Heterologous
Chemicals
5-(2,4-dihydroxy-5-isopropylphenyl)-4-(4-morpholin-4-ylmethylphenyl)isoxazole-3-carboxylic acid ethylamide Antineoplastic Agents HSP90 Heat-Shock Proteins Isoxazoles Resorcinols
Authors & Affiliations
37 authors, click to expand affiliations / ORCID
Brough Paul A
Vernalis Ltd., Granta Park, Great Abington, Cambridge CB21 6GB, U.K. p.brough@ vernalis.com
Aherne Wynne
Barril Xavier
Borgognoni Jenifer
Boxall Kathy
Cansfield Julie E
Cheung Kwai-Ming J
Collins Ian
Davies Nicholas G M
Drysdale Martin J
Dymock Brian
Eccles Suzanne A
Finch Harry
Fink Alexandra
Hayes Angela
Howes Robert
Hubbard Roderick E
James Karen
Jordan Allan M
Lockie Andrea
Martins Vanessa
Massey Andrew
Matthews Thomas P
McDonald Edward
Northfield Christopher J
Pearl Laurence H
Prodromou Chrisostomos
Ray Stuart
Raynaud Florence I
Roughley Stephen D
Sharp Swee Y
Surgenor Allan
Walmsley D Lee
Webb Paul
Wood Mike
Workman Paul
Wright Lisa
Article Info
Journal
Journal of medicinal chemistry
Abbr.
J Med Chem
ISSN
0022-2623
Published
2008-01-24
Epub
2007-00-20
Pages
196-218
Language
English
Region
United States
NLM ID
9716531
Subset
IM
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