Discovery of novel aminoquinazolin-7-yl 6,7-dihydro-indol-4-ones as potent, selective inhibitors of heat shock protein 90-Reference-Cited by-同舟云学术

Discovery of novel aminoquinazolin-7-yl 6,7-dihydro-indol-4-ones as potent, selective inhibitors of heat shock protein 90

Published:2012-04 Issue:7 Volume:22 Page:2550-2554
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Huang Kenneth H.,Barta Thomas E.,Rice John W.,Smith Emilie D.,Ommen Andy J.,Ma Wei,Veal James M.,Fadden R. Patrick,Barabasz Amy F.,Foley Briana E.,Hughes Philip F.,Hanson Gunnar J.,Markworth Christopher J.,Silinski Melanie,Partridge Jeffrey M.,Steed Paul M.,Hall Steven E.

Publisher

Elsevier BV

Subject

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

Reference50 articles.

1. HSP90 as a new therapeutic target for cancer therapy: the story unfolds

2. Inhibitors of HSP90 and other chaperones for the treatment of cancer

3. Heat shock protein 90 as a molecular target for cancer therapeutics

4. Hsp90: the vulnerable chaperone

5. HSP90 and the chaperoning of cancer

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