A potent inhibitor of IgE-mediated mast cell responses to allergens in vitro and in vivo. Also inhibits cyclin-dependent kinase 2 (Cdk2; IC50 = 1 µM) by blocking the ATP site.
A potent inhibitor of lgE-mediated mast cell responses to allergens in vitro and in vivo. Also inhibits cyclin-dependent kinase 2 (Cdk2; IC50 = 1 µM) by blocking the ATP site.
生物化学的/生理学的作用
Cell permeable: no
Primary Target Cdk2
Product does not compete with ATP.
Reversible: no
Target IC50: 1 µM for Cdk2
包装
Packaged under inert gas
警告
Toxicity: Standard Handling (A)
再構成
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
その他情報
Shewchuk, L., et al. 2000. J. Med. Chem. 43, 133. Chen, C.L., et al. 1999. Pharm. Res. 16, 117.
法的情報
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany