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SML4455

Y-27632 2HCl ≥ 99% by HPLC

≥99% (HPLC)

Synonym(e):

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

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Über diesen Artikel

Empirische Formel (Hill-System):
C14H21N3O·2HCl
CAS-Nummer:
Molekulargewicht:
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

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Dieser Artikel
Y0503688000SCM075
description

≥99% (HPLC)

description

≥98% (HPLC)

description

Y-27632A, CAS 331752-47-7, is a cell-permeable, reversible, inhibitor of Rho kinases (Ki = 140 nM for p160ROCK). Enhances survival & cloning efficiency of ESC without affecting their pluripotency.

description

The ROCK Inhibitor (Y-27632) is available in a 5 mg format & has been optimized & validated for cell culture & Neuroscience applications.

assay

≥99% (HPLC)

assay

≥98% (HPLC)

assay

≥95% (HPLC)

assay

-

form

powder

form

powder

form

solid

form

lyophilized

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

-10 to -25°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

-10 to -25°C

solubility

H2O: 2 mg/mL, clear

solubility

H2O: 14 mg/mL

solubility

water: 100 mg/mL

solubility

-

storage condition

desiccated

storage condition

-

storage condition

OK to freeze, protect from light, desiccated (hygroscopic)

storage condition

-


Lagerklasse

11 - Combustible Solids

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable



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