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- 保质期:
包装说明
- 英文名:
Y-27632 . dihydrochloride
- 库存:
大量
- 供应商:
Neobioscience
- CAS号:
146986-50-7
- 保存条件:
-20
- 规格:
1*25mg
货号:ALX-270-333-M025
规格:25mg
Y-27632 . dihydrochloride产品简介:
High potency inhibitor of smooth muscle contractions
Applications in nephrology, stem cell studies, cardiovascular, cancer, and neurology
Highly cited
Y-27632 is a highly potent, cell permeable, selective and ATP competitive inhibitor of ROCK1 and ROCK2 (IC50=800nM). It acts as a potent inhibitor of agonist-induced Ca2+sensitization of myosin phosphorylation and smooth muscle contractions, blocking cell spreading and suppresses RhoA-induced formation of stress fibers in hepatic stellate cells. Y-27632 significantly reduces the increase of inflammatory cytokines after reperfusion, preventing the development of acute renal failure. There are numerous application for this compound including: cardioprotective effects, suppression of tumor cell invasion, inhibition of superoxide production, mimicking effect of β-agonists on human cells, and an antinociceptive effect.
There has been a growing interest in Y-27632 for use in stem cell self-renewal and reprogramming. It is known to increase the survival rate of human embryonic stem cells undergoing cryopreservation.
Product Details
Alternative Name: (R)-(+)-trans-N-(4-Pyridyl)-4-(1-aminoethyl)-cyclohexanecarboxamide . 2HCl
Formula: C14H21N3O . 2HCl
MW: 247.3 . 73.0
CAS: 129830-38-2
Purity: ≥98% (HPLC (UV))
Purity Detail: Enantiomeric excess ≥96%
Identity: Determined by MS and NMR.
Appearance: White to pale yellow powder.
Solubility: Soluble in DMSO (25mg/ml), methanol (25mg/ml), acetonitrile (<1mg/ml), dioxan (<1mg/ml), water (very soluble).
Shipping: Ambient
Long Term Storage: -20°C
Use/Stability: Stock solutions are stable for up to 1 month when stored at -20°C.
Handling: Protect from light. Packaged under inert gas. After reconstitution, prepare aliquots and store at -20°C.
Regulatory Status: RUO - Research Use Only
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assay qHTS) ,通过CTG(CELL TITER-GLO)发光法评估15, 333种化合物对细胞活力的影响,发现总共有113种类型能够提高细胞存活率。而其中Chroman 1对ROCK通路比Y-27632具有更好的抑制效果和选择性。随后,作者从113个活性化合物中,挑选了29个作用不同靶点的化合物进行了组合小分子基质筛选(Combinatorial small-molecule matrix screening),发现Chroman 1与Caspase阻滞剂Emricasan有显著的协同
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