The discovery of potent cRaf1 kinase inhibitors-Reference-Cited by-同舟云学术

The discovery of potent cRaf1 kinase inhibitors

Published:2000-02 Issue:3 Volume:10 Page:223-226
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Lackey Karen,Cory Michael,Davis Ronda,Frye Stephen V.,Harris Philip A.,Hunter Robert N.,Jung David K.,McDonald O.Bradley,McNutt Robert W.,Peel Michael R.,Rutkowske Randy D.,Veal James M.,Wood Edgar R.

Publisher

Elsevier BV

Subject

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

Reference21 articles.

1. Serine- and threonine-specific protein kinase activities of purified gag–mil and gag–raf proteins

2. Raf-1 protein kinase is required for growth of induced NIH/3T3 cells

3. Antitumor activity of a phosphorothioate antisense oligodeoxynucleotide targeted against C-raf kinase

Cited by 200 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. Discovery and Anticancer Screening of Novel Oxindole-Based Derivative Bearing Pyridyl Group as Potent and Selective Dual FLT3/CDK2 Kinase Inhibitor;Pharmaceuticals;2024-05-20

2. Perspectives of autophagy-tethering compounds (ATTECs) in drug discovery;Medicine Plus;2024-03

3. Discovery of pyrazolo[3,4-d]pyrimidines as novel mitogen-activated protein kinase kinase 3 (MKK3) inhibitors;Bioorganic & Medicinal Chemistry;2024-01

4. Discovery of a Drug-like, Natural Product-Inspired DCAF11 Ligand Chemotype;Nature Communications;2023-11-30

5. Solvent impact on the photochemical properties of anticancer drug PLX4720; a computational study;Inorganic Chemistry Communications;2023-11