19 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Cyclin Dependent Kinase 9 Inhibitors for Cancer Therapy.

University of Nebraska Medical Center
Discovery of potent and bioavailable GSK-3beta inhibitors.

Roche Palo Alto
A quantitative analysis of kinase inhibitor selectivity.

Ambit Biosciences
Comprehensive analysis of kinase inhibitor selectivity.

Ambit Biosciences
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML).

Ambit Biosciences
From a natural product lead to the identification of potent and selective benzofuran-3-yl-(indol-3-yl)maleimides as glycogen synthase kinase 3beta inhibitors that suppress proliferation and survival of pancreatic cancer cells.

University of Illinois At Chicago
Discovery of a Dual Tubulin and Neuropilin-1 (NRP1) Inhibitor with Potent In Vivo Anti-Tumor Activity via Pharmacophore-based Docking Screening, Structure Optimization, and Biological Evaluation.

China Pharmaceutical University
Discovery of Novel

Shenyang Pharmaceutical University
CDK9 inhibitors in cancer research.

Nankai University
2-Aminothiazole: A privileged scaffold for the discovery of anti-cancer agents.

Hunan University of Science and Technology
Lessons Learned from Past Cyclin-Dependent Kinase Drug Discovery Efforts.

Hefei University of Technology
Therapeutic potential of quinazoline derivatives for Alzheimer's disease: A comprehensive review.

University of Louisiana At Lafayette
Development and Therapeutic Potential of NUAKs Inhibitors.

University of Science and Technology (Ust)
Discovery of AZD4573, a Potent and Selective Inhibitor of CDK9 That Enables Short Duration of Target Engagement for the Treatment of Hematological Malignancies.

Astrazeneca
Discovery of Inhibitors of Aurora/PLK Targets as Anticancer Agents.

Chengdu University
Cyclin-Dependent Kinase 2 Inhibitors in Cancer Therapy: An Update.

University of South Australia Cancer Research Institute
Carbocyclic sulfone RORγ modulators

Bristol-Myers Squibb
Pharmacological characterization of the human ionotropic glutamate receptor subtype GluR3 stably expressed in mammalian cells.

Sibia Neurosciences