CDK2/cyclinA inhibitors: Targeting the cyclinA recruitment site with small molecules derived from peptide leads-Reference-Cited by-同舟云学术

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CDK2/cyclinA inhibitors: Targeting the cyclinA recruitment site with small molecules derived from peptide leads

Published:2006-03 Issue:6 Volume:16 Page:1716-1720
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Castanedo Georgette,Clark Kevin,Wang Shumei,Tsui Vickie,Wong Mengling,Nicholas John,Wickramasinghe Dineli,Marsters James C.,Sutherlin Daniel

Publisher

Elsevier BV

Subject

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

Reference15 articles.

1. Crystal structure of the p27Kip1 cyclin-dependent-kinase inibitor bound to the cyclin A–Cdk2 complex

2. Tossing monkey wrenches into the clock: New ways of treating cancer

3. Selective killing of transformed cells by cyclin/cyclin-dependent kinase 2 antagonists

4. Identification of E2F-1/Cyclin A antagonists

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1. Cyclin A/B RxL Macrocyclic Inhibitors to Treat Cancers with High E2F Activity;2024-08-01

2. Strategies for converting turn-motif and cyclic peptides to small molecules for targeting protein–protein interactions;RSC Chemical Biology;2024

3. Single-Pulse Shock Tube Pyrolysis Study of RP-3 Jet Fuel and Kinetic Modeling;ACS Omega;2021-04-14

4. Cyclin-dependent kinase 2 (Cdk2) controls phosphatase-regulated signaling and function in platelets;2020-06-01

5. Effect of Structural Descriptors on the Design of Cyclin Dependent Kinase Inhibitors Using Similarity‐based Molecular Evolution;Molecular Informatics;2020-01-23

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