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KB-0742

KB-0742 is a potent, selective and orally active CDK9 inhibitor with an IC50 of 6 nM for CDK9/cyclin T1. KB-0742 is selective for CDK9/cyclin T1 with >50-fold selectivity over other CDK kinases. KB-0742 has potent anti-tumor activity[1][2].

Product Specifications

CAS Number

[2416873-83-9]

UNSPSC

12352005

Target

CDK

Type

Reference compound

Related Pathways

Cell Cycle/DNA Damage

Applications

Cancer-Kinase/protease

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/kb-0742.html

Concentration

10mM

Purity

99.38

Solubility

DMSO : 175 mg/mL (ultrasonic)

Smiles

N[C@@H]1C[C@@H](NC2=CC(C(CC)CC)=NC3=CC=NN23)CC1

Molecular Formula

C16H25N5

Molecular Weight

287.40

References & Citations

[1]André Richters, et al. Modulating Androgen Receptor-Driven Transcription in Prostate Cancer with Selective CDK9 Inhibitors. Cell Chem Biol. 2020 Oct 20; S2451-9456 (20) 30380-9.|[2]Freeman DB, et al. Discovery of KB-0742, a Potent, Selective, Orally Bioavailable Small Molecule Inhibitor of CDK9 for MYC-Dependent Cancers. J Med Chem. 2023 Dec 14;66 (23) :15629-15647.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

Phase 2

Isoform

CDK1; CDK2; CDK3; CDK4; CDK5; CDK6; CDK7; CDK8; CDK9

Citation 01

University of California, Irvine. 2024.|bioRxiv. 2025 Nov 3:2025.11.02.685764.|Cell Chem Biol. 2025 Apr 17;32 (4) :542-555.e10.

Available Sizes

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