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Merck
CN

SML4455

Y-27632 2HCl ≥ 99% by HPLC

≥99% (HPLC)

别名:

ROCK Inhibitor, Rho-Associated Kinases Inhibitor, trans-4-[(R)-1-Aminoethyl]-N-(4-pyridyl)cyclohexanecarboxamide dihydrochlorid

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关于此项目

经验公式(希尔记法):
C14H21N3O·2HCl
化学文摘社编号:
分子量:
320.26
UNSPSC Code:
12352200
Assay:
≥99% (HPLC)
Form:
powder
Storage condition:
desiccated
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Quality Segment

assay

≥99% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

H2O: 2 mg/mL, clear

storage temp.

-10 to -25°C

Biochem/physiol Actions

Y-27632 is a reversible, cell-permeable, ATP-competitive inhibitor of ROCK-I and ROCK-II (Ki~0.2–0.3 μM) that targets the catalytic cleft to fundamentally modulate cytoskeletal mechanics. By blocking actomyosin contractility, it induces the disassembly of actin stress fibers and focal adhesions, preventing membrane blebbing and driving potent smooth muscle relaxation (IC50~0.3–1.0 μM). While effective in hypertensive models, its systemic utility is constrained by rapid clearance and the risk of profound hypotension, often necessitating local administration. Consequently, its therapeutic potential is best realized in specialized tissues: Y27632 crosses the blood-brain barrier to promote axon regeneration and prevent growth cone collapse in CNS injury, and in ophthalmology, it lowers intraocular pressure and aids corneal endothelial healing. Beyond these in vivo applications, Y-27632 is the industry standard for ex vivo cell manipulation, particularly in cancer biology to inhibit metastasis and, most significantly, in stem cell research. Here, Y-27632 prevents dissociation-induced apoptosis (anoikis) in human pluripotent stem cells (hESCs/iPSCs), revolutionizing single-cell cloning, enzymatic passaging, and graft viability in regenerative medicine.

Disclaimer

Hygroscopic, Store with desiccant


存储类别

11 - Combustible Solids

闪点 (F)

Not applicable

闪点 (°C)

Not applicable



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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