Taizhou Crene Biotechnology Co., Ltd.
                                                                                                           
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Cas 602306-29-6 AZD5438 CDK Inhibitors Cyclin Dependent Kinase Inhibitors

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Product Description

Cas 602306-29-6 AZD5438 CDK Inhibitors Cyclin Dependent Kinase Inhibitors

 

+ AII PRODUCTS

- Prostaglandins - Custom Synthesis - PARP Inhibitors - PI3K Inhibitors - FAK Inhibitors - AKT Inhibitors - C-Kit Inhibitors - VEGFR Inhibitors - c-Met Inhibitors - CDK Inhibitors - CYP17 Inhibitors - DNA/RNA Inhibitors - mTOR Inhibitors - SRC Inhibitors - Others

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Chemical Information

Product name:AZD5438

Purity:98% min

CAS NO:602306-29-6

Solubility:DMSO100 mg/mL (269.21 mM)

Molecular Formula:C18H21N5O2S

Package:Package according to customer requirements

Molecular Weight:371.457

Storage:Store at -20℃

 

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Remarks

AZD5438 is a potent inhibitor of cyclin-dependent kinase (cdk) 1, 2, and 9 (IC(50), 16, 6, and 20 nmol/L, respectively). In vitro, AZD5438 showed significant antiproliferative activity in human tumor cell lines (IC(50) range, 0.2-1.7 micromol/L), causing inhibition of the phosphorylation of cdk substrates pRb, nucleolin, protein phosphatase 1a, and RNA polymerase II COOH-terminal domain and blocking cell cycling at G(2)-M, S, and G(1) phases.

 

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References

[1].Byth KF, et al. AZD5438, a potent oral inhibitor of cyclin-dependent kinases 1, 2, and 9, leads to pharmacodynamic changes and potent antitumor effects in human tumor xenografts. Mol Cancer Ther. 2009 Jul;8(7):1856-66. Epub 2009 Jun 9.

[2].Raghavan P, et al. AZD5438, an Inhibitor of Cdk1, 2, and 9, Enhances the Radiosensitivity of Non-Small Cell Lung Carcinoma Cells. Int J Radiat Oncol Biol Phys. 2012 Jul 12.

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