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- Y-27632 146986-50-7

- Y-27632 146986-50-7
Y-27632 146986-50-7
产品描述 描述 Y-27632 is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM in a cell-free assay, exhibits >200-fold selectivity over Others kinases, including PKC, cAMP-dependent protein kinase, MLCK and PAK.
纯度 ≥98%储存/保存方法 Store at -20℃ for three years(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.基本信息 别名 Y 27632;Y-27632外观 White Powder可溶性/溶解性 DMSO : ≥ 32 mg/mL (129.38 mM)生物活性 靶点 ROCK-I;ROCK-II;PKN;PKCα;PKA;Citron kinaseIn vitro(体外研究) Y-27632 inhibits the ROCK family of kinases 100 times more potently than other kinases including protein kinase C, cAMP-dependent kinase and myosin light chain kinase. Y-27632 prolongs the lag time and delays the appearance of BrdU-labeled cells in a concentration-dependent manner, delays of about 1 and 4 h are noticed in the Swiss 3T3 cells treated with 10 and 100 μM Y-27632, respectively. Y-27632 promotes neuronal differentiation of adipose tissue-derived stem cells (ADSCs). Compared to 1.0 and 2.5 µM Y-27632 induced groups, percentages of neuroal-like cells achieved a peak in the 5.0 µM Y-27632 induced group.In vivo(体内研究) Y-27632 (5 and 10 mg/kg) significantly prolongs the onset time of myoclonic jerks when compare with saline group. Y-27632 (5 and 10 mg/kg) significantly prolongs the onset time of clonic convulsions when compare with saline group. Treatment with Dimethylnitrosamine (DMN) causes a significant decrease in rat body and liver weight (DMN-S group) compared with control animals (S-S group). Oral Y27632 (30 mg/kg) essentially prevents this DMN-induced rat body and liver weight loss (DMN-Y group).研究领域 研究领域 Stem CellsSignaling PathwaysDrug DiscoverySmall Molecule DrugLead Compound DiscoveryY-27632 146986-50-7温馨提示:本产品仅作科研实验使用,不支持临床等研究
