Comparison

AZD5438 European Partner

Item no. M1810-200mg
Manufacturer AbMole
CASRN 602306-29-6
Amount 200mg
Category
Type Inhibitors
Specific against other
Purity >99%
Citations 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. Byth KF, et al . Mol Cancer Ther. 2009 Jul,8(7):1856-66. PMID: 19509270 . A phase I pharmacodynamic study of the effects of the cyclin-dependent kinase-inhibitor AZD5438 on cell cycle markers within the buccal mucosa, plucked scalp hairs and peripheral blood mononucleocytes of healthy male volunteers. Camidge DR, et al . Cancer Chemother Pharmacol. 2007 Sep,60(4):479-88. PMID: 17143601 .
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias AZD 5438
Similar products AZD5438, AZD 5438
Available
Target Information
CDK
Molecular Weight
371, 46
Solubility
DMSO 64 mg/mL; Ethanol 54 mg/mL
Bioactivity information
AZD5438 is a novel, orally bioavailable inhibitor of cyclin-dependent kinase (CDK) 1, 2 and 9 (IC50 values are 16, 6 and 20 nM respectively).

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 200mg
Available: In stock
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