3D Pharmacophore Model-Assisted Discovery of Novel CDC7 Inhibitors-Reference-Cited by-同舟云学术

3D Pharmacophore Model-Assisted Discovery of Novel CDC7 Inhibitors

Published:2011-08-02 Issue:10 Volume:2 Page:720-723
ISSN:1948-5875
Container-title:ACS Medicinal Chemistry Letters
language:en
Short-container-title:ACS Med. Chem. Lett.

Author:

Lindvall Mika¹,McBride Christopher¹,McKenna Maureen¹,Gesner Thomas G.¹,Yabannavar Asha¹,Wong Kent¹,Lin Song¹,Walter Annette¹,Shafer Cynthia M.¹

Affiliation:

1. Global Discovery Chemistry/Oncology & Exploratory Chemistry, Novartis Institutes for Biomedical Research, 4560 Horton Street, Emeryville, California 94608, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ml200029w

Reference26 articles.

1. Mammalian Cdc7-Dbf4 protein kinase complex is essential for initiation of DNA replication

2. Functions of mammalian Cdc7 kinase in initiation/monitoring of DNA replication and development

3. Bipartite Binding of a Kinase Activator Activates Cdc7-related Kinase Essential for S Phase

4. Cell cycle regulation of chromatin binding and nuclear localization of human Cdc7-ASK kinase complex

5. Drf1, a novel regulatory subunit for human Cdc7 kinase

Cited by 25 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Design, Synthesis, Anticancer Evaluation and Molecular Docking Studies of Amide Derivatives of Thienopyrimidine Isoxazoles;Organic Preparations and Procedures International;2024-03-13

2. MMP9 in Pan-Cancer and Computational Study to Screen MMP9 Inhibitors;2023-02-28

3. Induced-Fit Docking Enables Accurate Free Energy Perturbation Calculations in Homology Models;Journal of Chemical Theory and Computation;2022-08-16

4. Design, synthesis and biological evaluation of aryl and hetero-aryl linked thieno[3,2-d]pyrimidine derivatives as anticancer agents;Chemical Data Collections;2022-06

5. Recent advances in transition metal-catalyzed heteroannulative difunctionalization of alkenes via C–H activation for the synthesis of heterocycles;Organic Chemistry Frontiers;2022