溶解性 | 25°C: DMSO |
存贮条件 | 储存温度2-8℃ |
应用 | A cell permeable, highly specific, and potent ATP-competitive inhibitor of ρ-kinase inhibitor。 |
产品介绍 | H-1152是特异的高活性Rho激酶抑制剂,可渗透入细胞膜,Ki为1.6 nM,对其它丝氨酸/苏氨酸激酶抑制性极低。 |
生化机理 | H-1152 is a selective ATP-competitive inhibitor of rho-kinase (ROCK) inhibitor, cell permeable, highly specific, and potent (Ki = 1.6 nM). Exhibits weaker affinity for other serine/threonine kinases (Ki = 630 nM for PKA, 9.27mM for PKC and 10.1 mM for MLCK) and is more potent and selective than Y-27632. Inhibits the phosphorylation of MARCKS in cells stimulated by lysophosphatidic acid and inhibits EP3-stimulated NO formation. H-1152 . dihydrochloride prevents fragmentation of apoptotic cells. Relieves neuropathic pain. |
别名 | H 1152;H1152;4-甲基-5-{[(2S)-2-甲基-1,4-二氮杂环庚-1-基]磺酰基}异喹啉;H 1152;H1152; 4-methyl-5-{[(2s)-2-methyl-1,4-diazepan-1-yl]sulfonyl}isoquinoline ;(S)-(+)-2-Methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]homopiperazine |
H-1152,ROCK 抑制剂
H-1152 (订货以英文为准)
编号:H125533
CAS号:451462-58-1
分子式:C16H21N3O2S
分子量:319.42
产品名称 | H-1152 |
中文名称 | H-1152,ROCK 抑制剂 |
CAS号 | 451462-58-1 |
分子式(M.F.) | C16H21N3O2S |
分子量(M.W.) | 319.42 |
储存条件 | 2-8°C储存 |
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