Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3-Reference-Cited by-同舟云学术

Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3

Published:2004-01 Issue:2 Volume:14 Page:343-346
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Yue Eddy W.,DiMeo Susan V.,Higley C.Anne,Markwalder Jay A.,Burton Catherine R.,Benfield Pamela A.,Grafstrom Robert H.,Cox Sarah,Muckelbauer Jodi K.,Smallwood Angela M.,Chen Haiying,Chang Chong-Hwan,Trainor George L.,Seitz Steven P.

Publisher

Elsevier BV

Subject

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

Reference13 articles.

1. Contributions in the domain of cancer research: Review¶Negative regulators of cyclin-dependent kinases and their roles in cancers

2. Cell Cycle Regulation in the G1 Phase: A Promising Target for the Development of New Chemotherapeutic Anticancer Agents

3. Inhibition of CDKs as a Therapeutic Modality

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