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MC180295

MC180295 ((rel) -MC180295) is a potent and selective CDK9-Cyclin T1 inhibitor, with an IC50 of 5 nM, at least 22-fold more selective for CDK9 over other CDKs. MC180295 also inhibits GSK-3α and GSK-3β. MC180295 ((rel) -MC180295) has potent anti-tumor effect[1].

Product Specifications

CAS Number

[2237942-08-2]

Product Name Alternative

(rel) -MC180295

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/_rel_-MC180295.html

Concentration

10mM

Purity

98.89

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

NC1=C(C(C2=CC=CC=C2[N+]([O-])=O)=O)SC(N[C@@H]3[C@H](C4)CC[C@H]4C3)=N1

Molecular Formula

C17H18N4O3S

Molecular Weight

358.41

References & Citations

[1]Zhang H, et al. Targeting CDK9 Reactivates Epigenetically Silenced Genes in Cancer. Cell. 2018 Nov 15;175 (5) :1244-1258.e26.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, stored under nitrogen)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

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

Available Sizes

Curated Selection

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