H-1152

CAT: 0804-HY-15720-01Size: 5 mgDry Ice: NoHazardous: No

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CAT#:0804-HY-15720-01Size:5 mg

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24/48H Stock Items & 2 to 6 Weeks non Stock Items.

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Description

H-1152 is a membrane-permeable and selective ROCK inhibitor, with a Ki value of 1.6 nM, and an IC50 value of 12 nM for ROCK2.

CAS Number

451462-58-1

UNSPSC

12352005

Hazard Statement

H302-H315-H319-H335

Target

ROCK

Type

Reference compound

Related Pathways

Cell Cycle/DNA Damage; Cytoskeleton; Stem Cell/Wnt; TGF-beta/Smad

Applications

Neuroscience-Neuromodulation

Field of Research

Neurological Disease

Assay Protocol

https://www.medchemexpress.com/h-1152.html

Purity

98.63

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

CC1=CN=CC2=C1C(S(=O)(N3[C@@H](C)CNCCC3)=O)=CC=C2

Molecular Formula

C16H21N3O2S

Molecular Weight

319.42

Precautions

P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

References & Citations

[1]Tamura M, et al. Development of specific Rho-kinase inhibitors and their clinical application. Biochim Biophys Acta. 2005 Dec 30;1754 (1-2) :245-52. Epub 2005 Sep 12.|[2]Ikenoya M, et al. Inhibition of rho-kinase-induced myristoylated alanine-rich C kinase substrate (MARCKS) phosphorylation in human neuronal cells by H-1152, a novel and specific Rho-kinase inhibitor. J Neurochem. 2002 Apr;81 (1) :9-16.|[3]Lie M, et al. Accelerated neurite growth from spiral ganglion neurons exposed to the Rho kinase inhibitor H-1152. Neuroscience. 2010 Aug 25;169 (2) :855-62.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

Phase 2

Isoform

ROCK2

Citation 01

Acta Neuropathol Commun. 2024 Sep 14;12 (1) :150.|bioRxiv. 2025 May 09.|Research Square Preprint. 2021 Jun.|University of Toronto. 2026.

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