TRANS-4-[(1R)-1-AMINOETHYL]-N-4-PYRIDINYLCYCLOHEXANECARBOXAMIDE DIHYDROCHLORIDE - Names and Identifiers
TRANS-4-[(1R)-1-AMINOETHYL]-N-4-PYRIDINYLCYCLOHEXANECARBOXAMIDE DIHYDROCHLORIDE - Physico-chemical Properties
Molecular Formula | C14H21N3O
|
Molar Mass | 247.34 |
Density | 1.136±0.06 g/cm3(Predicted) |
Melting Point | >260°C (dec.) |
Boling Point | 462.6±15.0 °C(Predicted) |
Solubility | DMSO:50 mg/mL |
Appearance | solid |
Color | white |
pKa | 13.53±0.40(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,2-8°C |
Stability | Hygroscopic |
Use | This product is for scientific research only and shall not be used for other purposes. |
In vitro study | Y-27632 inhibits the ROCK family of kinases 100 times more potently than other kinases including protein kinase C, cAMP-dependent kinase and myosin light chain kinase. Y-27632 prolongs the lag time and delays the appearance of BrdU-labeled cells in a concentration-dependent manner, delays of about 1 and 4 h are noticed in the Swiss 3T3 cells treated with 10 and 100 μM Y-27632, respectively.
Y-27632 promotes neuronal differentiation of adipose tissue-derived stem cells (ADSCs). Compared to 1.0 and 2.5 μM Y-27632 induced groups, percentages of neuroal-like cells achieved a peak in the 5.0 μM Y-27632 induced group. |
In vivo study | Y-27632 (5 and 10 mg/kg) significantly prolongs the onset time of myoclonic jerks when compare with saline group. Y-27632 (5 and 10 mg/kg) significantly prolongs the onset time of clonic convulsions when compare with saline group. Treatment with Dimethylnitrosamine (DMN) causes a significant decrease in rat body and liver weight (DMN-S group) compared with control animals (S-S group). Oral Y27632 (30 mg/kg) essentially prevents this DMN-induced rat body and liver weight loss (DMN-Y group). |
TRANS-4-[(1R)-1-AMINOETHYL]-N-4-PYRIDINYLCYCLOHEXANECARBOXAMIDE DIHYDROCHLORIDE - Risk and Safety
Hazard Symbols | Xn - Harmful
|
Risk Codes | 20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
|
Safety Description | 36 - Wear suitable protective clothing.
|
WGK Germany | 3 |
TRANS-4-[(1R)-1-AMINOETHYL]-N-4-PYRIDINYLCYCLOHEXANECARBOXAMIDE DIHYDROCHLORIDE - Introduction
Y-27632 is a competitive ROCK-I and ROCK-II inhibitor of ATP, which Y-27632 induce human induced pluripotent stem cells (hIPSCs) to selectively differentiate into mesenchymal lineages through epithelial-mesenchymal transition-like regulation.
Last Update:2022-10-16 17:41:24
TRANS-4-[(1R)-1-AMINOETHYL]-N-4-PYRIDINYLCYCLOHEXANECARBOXAMIDE DIHYDROCHLORIDE - Reference Information
biological activity | Y-27632 are orally effective, ATP competitive ROCK-I and ROCK-II inhibitors, Ki is 220 nM and 300 nM respectively. Y-27632 induces apoptosis (apoptosis). Y-27632 human induced pluripotent stem cells (hIPSCs) selectively differentiate into mesenchymal lineages through epithelial-mesenchymal transition-like regulation. |
Last Update:2024-04-09 21:54:55