2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
生物活性
Description
In Vivo
In Vitro
化合物的使用
Kinase Assay
Cell Assay
Animal Administration
参考文献
Selective inhibitor of myosin light chain kinase (MLCK) (Ki = 0.3 μM). Exhibits more potent inhibition than the parent compound ML 9 hydrochloride. Displays reversible, ATP-competitive inhibition of Ca2+-calmodulin-dependent and -independent smooth muscle MLCKs.
For the detailed information about the solubility of ML-7 Hydrochloride in water, the solubility of ML-7 Hydrochloride in DMSO, the solubility of ML-7 Hydrochloride in PBS buffer, the animal experiment（test） of ML-7 Hydrochloride,the in vivo,in vitro and clinical trial test of ML-7 Hydrochloride,the cell experiment（test） of ML-7 Hydrochloride,the IC50, EC50 and Affinity of ML-7 Hydrochloride, please contact DC Chemicals.
