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H-1152

Chemical Structure : H-1152

CAS No.: 451462-58-1

H-1152 (H 1152, H1152)

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.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 319.4218
Formula C16H21N3O2S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Isoquinoline, 5-[[(2S)-hexahydro-2-methyl-1H-1,4-diazepin-1-yl]sulfonyl]-4-methyl-

References

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.

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