Chemical Structure : H-1152
CAS No.: 451462-58-1
Catalog No.: PC-44656Not For Human Use, Lab Use Only.
H-1152 is a potent and selective ROCK inhibitor with Ki of 1.6 nM.
Packing | Price | Stock | Quantity |
---|---|---|---|
5 mg | $158 | In stock | |
10 mg | $248 | In stock | |
25 mg | $428 | In stock | |
50 mg | Get quote | ||
100 mg | Get quote |
Bulk size, bulk discount!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
H-1152 is a potent and selective ROCK inhibitor with Ki of 1.6 nM.
H-1152 shows poor inhibition on other serine/threonine kinases.
H-1152 inhibits the phosphorylation of MARCKS in human neuroteratoma (NT-2) cells stimulated by Rho-activator lysophosphatidic acid.
M.Wt | 319.4218 | |
Formula | C16H21N3O2S | |
Appearance | Solid | |
Storage |
|
|
Solubility |
10 mM in DMSO |
|
Chemical Name/SMILES |
Isoquinoline, 5-[[(2S)-hexahydro-2-methyl-1H-1,4-diazepin-1-yl]sulfonyl]-4-methyl- |
1. Ikenoya M, et al. J Neurochem. 2002 Apr;81(1):9-16.
2. Wang HL, et al. Neuropharmacology. 2013 Jul;70:1-11.
3. Sheikh IA, et al. J Biol Chem. 2013 Jul 12;288(28):20404-15.
Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright