Y-27632 dihydrochloride

Properties

Biological source: synthetic (organic)

Quality level: 100

Test: ≥98% (HPLC)

Form: dust

Optical activity

[α] / D +3.5 to + 5.0 °, c = 0.5 in methanol

Colour: white to beige

Solubility: H2O: 14 mg / ml

Storage temperature: 2-8 ° C

SMILES chain

Cl.Cl.C [C @@ H] (N) [C @ H] 1CC [C @@ H] (CC1) C (= O) Nc2ccncc2

InChI

1S / 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 – ;; / m1 ../ s1

General description

Y-27632 dihydrochloride is an effective bronchodilator and improves antigen- and acetylcholine-induced lung resistance (RL). Y-27632 controls neutrophil migration and pulmonary edema and maybe a potential drug to treat acute lung injury.

Request

Y-27632 dihydrochloride has been used:

  • as a medium supplement in the organoid culture of pancreatic ductal adenocarcinoma
  • in the inhibition of Ras (Rho) homologous gene family 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 (iPSC)

Packaging

1.5mg in a glass bottle

Biochemical / Physiological Actions

Y-27632 is a highly potent and cell-permeable selective inhibitor of ROCK (serine protein/threonine kinase / Rho-associated spiral forming spiral-forming protein). Ki = 140 nM for p160ROCK. Y-27632 also inhibits ROCK-II with the same power. The inhibition is competitive with respect to ATP.

Features and Benefits

  • This compound is a featured product for phosphatase kinase biology research.
  • This compound is also offered as part of Sigma’s Library of Pharmacologically Active Compounds (LOPAC®1280), a biological annotation collection of high-quality, ready-to-test compounds.

 

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