17 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Comprehensive analysis of kinase inhibitor selectivity.

Ambit Biosciences
Design, Synthesis, and Biological Evaluation of Novel Orally Available Covalent CDK12/13 Dual Inhibitors for the Treatment of Tumors.

Insilico Medicine Shanghai Ltd
An update on small molecule compounds targeting synthetic lethality for cancer therapy.

Sichuan University
Discovery of novel imidazo[1,2-b]pyridazine derivatives as potent covalent inhibitors of CDK12/13.

Guizhou Medical University
Discovery of the SMYD3 Inhibitor BAY-6035 Using Thermal Shift Assay (TSA)-Based High-Throughput Screening.

Bayer AG
Pharmacological inhibition of BMK1 suppresses tumor growth through promyelocytic leukemia protein.

The Scripps Research Institute
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family.

Johann Wolfgang Goethe University
Targeting cyclin-dependent kinases: From pocket specificity to drug selectivity.

Shenyang Pharmaceutical University
Research progress of anticancer drugs targeting CDK12.

Qilu University of Technology
CDK9 inhibitors in cancer research.

Nankai University
Lessons Learned from Past Cyclin-Dependent Kinase Drug Discovery Efforts.

Hefei University of Technology
Current progress and novel strategies that target CDK12 for drug discovery.

West China Hospital
Synthetic Lethality through the Lens of Medicinal Chemistry.

Istituto Italiano Di Tecnologia
Recent development of CDK inhibitors: An overview of CDK/inhibitor co-crystal structures.

The First Affiliated Hospital of Zhengzhou University
CDK7 Inhibitors in Cancer Therapy: The Sweet Smell of Success?

Lebanese American University
STABLE CRYSTAL OF 4-OXOQUINOLINE COMPOUND

Japan Tobacco
Alkynyl pyridine prolyl hydroxylase inhibitor, and preparation method and medical use thereof

Jiangsu Hengrui Medicine