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Y-27632 dihydrochloride

Y-27632 dihydrochloride Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:Y27632 (hydrochloride)
CAS:129830-38-2
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: Biochempartner
Tel: 0086-13720134139
Email: candy@biochempartner.com
Products Intro: Product Name:Y-27632 dihydrochloride
CAS:129830-38-2
Purity:98% HPLC LCMS Package:10G;20G
Company Name: Accela ChemBio Inc.
Tel: +1-858-6993322
Email: info@accelachem.com
Products Intro: Product Name:trans-4-[(R)-1-Aminoethyl]-N-(4-pyridyl)cyclohexanecarboxamide Dihydrochloride
CAS:129830-38-2
Purity:>98% Package:0.25g Remarks:SY071527
Company Name: Shandong chuangyingchemical Co., Ltd.
Tel: 18853181302
Email: sale@chuangyingchem.com
Products Intro: Product Name:Y27632 (hydrochloride)
CAS:129830-38-2
Company Name: BOC Sciences
Tel: +1-631-485-4226
Email: inquiry@bocsci.com
Products Intro: Product Name:Y-27632 2HCl
CAS:129830-38-2
Purity:>98% Package:50 mg Remarks:Please reach out to us for more information about custom solutions.

Y-27632 dihydrochloride manufacturers

Y-27632 dihydrochloride Basic information
Product Name:Y-27632 dihydrochloride
Synonyms:Y-27632; Y27632; Y 27632;CS-1919;Y-27632; Y27632; Y 27632;Y 27632 DIHYDROCHLORIDE;Y27632 DIHYDROCHLORIDE;Y-27632 dihydrochloride, 98.5%, a selective ROCK1 (p160ROCK) inhibitor;(R)-4-(1-aminoethyl)-N-(pyridin-4-yl)cyclohexanecarboxamide dihydrochloride;Y-27632 DIHYDROCHLORIDE;ROCK INHIBITOR;Y-27632 dihydrochloride, >=98%;trans-4-[(R)-1-Aminoethyl]-N-(4-pyridyl)cyclohexanecarboxamide dihydrochloride Y 27632 dihydrochloride
CAS:129830-38-2
MF:C14H23Cl2N3O
MW:320.25792
EINECS:813-428-5
Product Categories:Inhibitors;APIs
Mol File:129830-38-2.mol
Y-27632 dihydrochloride Structure
Y-27632 dihydrochloride Chemical Properties
Melting point 258℃
storage temp. 2-8°C
solubility H2O: soluble14mg/mL
form powder
color white to beige
biological sourcesynthetic (organic)
Optical Rotation[α]/D +3.0 to +5.0°, c =1.0 in methanol
Water Solubility H2O: 14mg/mL
Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO or methanol may be stored at -20° for up to 3 months.
InChIInChI=1/C14H21N3O.2ClH/c1-10(15)11-2-4-12(5-3-11)14(18)17-13-6-8-16-9-7-13;;/h6-12H,2-5,15H2,1H3,(H,16,17,18);2*1H/t10-,11,12;;/s3
InChIKeyIDDDVXIUIXWAGJ-MEIAXHMCNA-N
SMILESC1(C(NC2=CC=NC=C2)=O)CCC([C@H](N)C)CC1.[H]Cl.[H]Cl |&1:13,r|
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22
Safety Statements 36
WGK Germany 3
HS Code 29333990
Storage Class11 - Combustible Solids
MSDS Information
Y-27632 dihydrochloride Usage And Synthesis
DescriptionY-27632 dihydrochloride (129830-38-2) is a specific inhibitor of ROCK family kinases.1 Enhances stem cell survival and proliferation in culture.2 Y-27632 dihydrochloride significantly improves freeze/thaw survival rate for human embryonic stem cells without influencing morphology, karyotype, cell surface markers, or differentiation potential.3
UsesA cell permeable inhibitor of ROCK-1 and ROCK-2
UsesY-27632 dihydrochloride has been used:
  • as a medium supplement in pancreatic ductal adenocarcinoma organoid culture
  • in the inhibition of Ras homolog gene family (Rho) kinase in mouse embryonic stem cells
  • in the inhibition of Rho-associated protein kinase (ROCK) in human embryonic stem cells and human induced pluripotent stem cells (iPSCs)

General DescriptionY-27632 dihydrochloride is an effective bronchodilator and improves lung resistance (RL) induced by antigen and acetylcholine. Y-27632 controls neutrophil migration and lung edema and may be a potential drug for treating acute lung injury.
Biochem/physiol ActionsY-27632 is highly potent, cell-permeable, selective ROCK (Rho-associated coiled coil forming protein serine/threonine kinase) inhibitor. Ki = 140 nM for p160ROCK. Y-27632 also inhibits ROCK-II with equal potency. The inhibition is competitive with respect to ATP.
storageDesiccate at RT
References[1] T ISHIZAKI. Pharmacological properties of Y-27632, a specific inhibitor of rho-associated kinases.[J]. Molecular Pharmacology, 2000, 57 5: 976-983.
[2] KALAMEGAM GAUTHAMAN  Ariff B  Chui Yee Fong. Effect of ROCK inhibitor Y-27632 on normal and variant human embryonic stem cells (hESCs) in vitro: its benefits in hESC expansion.[J]. Stem Cell Reviews and Reports, 2010, 6 1: 86-95. DOI:10.1007/s12015-009-9107-8
[3] XIANGYUN LI. The ROCK inhibitor Y-27632 enhances the survival rate of human embryonic stem cells following cryopreservation.[J]. Stem cells and development, 2008, 17 6: 1079-1085. DOI:10.1089/scd.2007.0247
[4] JEAN-DAVID MOREL. Proteomics Reveals Scope of Mycolactone-mediated Sec61 Blockade and Distinctive Stress Signature.[J]. Molecular & cellular proteomics : MCP, 2018: 1750-1765. DOI:10.1074/mcp.ra118.000824
[5] M. YAMAZAKI H M H Fujie. Chromatin condensation retains the osteogenic transcription factor, RUNX2, in the nucleus of human mesenchymal stem cells[J]. Journal of Biomechanical Science and Engineering, 1900, 1 1. DOI:10.1299/jbse.20-00083
Y-27632 dihydrochloride Preparation Products And Raw materials
Tag:Y-27632 dihydrochloride(129830-38-2) Related Product Information
Y-27632 YC-1 YKP-3089 BenzaMide, N-[4-chloro-3-(trifluoroMethyl)phenyl]-2-[2-(diMethylaMino)ethoxy]-6-ethoxy- N-[(3S,4R)-6-CYANO-3,4-DIHYDRO-3-HYDROXY-2,2-DIMETHYL-2H-1-BENZOPYRAN-4-YL]-N-HYDROXYACETAMIDE Y320 (R)-4-(1-Aminoethyl)-N-1H-pyrrolo[2,3-b]pyridin-4-ylbenzamide 3-(4-Pyridyl)indole Fasudil hydrochloride SB 431542 MG-132 CHIR-99021 YH239-EE YKL 06-061 YS 49 (R)-4-(1-aMinoethyl)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzaMide dihydrochloride PD 0325901 trans-4-MethoxycyclohexanaMine