Y-27632 dihydrochloride

Y-27632 dihydrochloride

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Y-27632 dihydrochloride

GK8578-5MG 5 mg
EUR 333

Y-27632 dihydrochloride

GK8578-1MG 1 mg
EUR 142

Y-27632 dihydrochloride

GK8578-25MG 25 mg
EUR 788

Y-27632 dihydrochloride

A3008-10 10 mg
EUR 142
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2.

Y-27632 dihydrochloride

A3008-200 200 mg
EUR 1070
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2.

Y-27632 dihydrochloride

A3008-5.1 10 mM (in 1mL DMSO)
EUR 148
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2.

Y-27632 dihydrochloride

A3008-50 50 mg
EUR 421
Description: Y-27632 dihydrochloride is a small-molecule inhibitor of Rho-associated protein kinase p160ROCK with the IC50 of 140 nM. Y-27632 suppresses the kinase activity of both ROCK-1 and ROCK-2 in vitro, and this compound inhibits the kinases by binding to the catalytic site of ROCK-1 and ROCK-2.

Y-27632

HY-10071 100mg
EUR 1234

Y-27632

E1KS1049 2 mg
EUR 325

Y 27632

20-abx076548
  • EUR 272.00
  • EUR 523.00
  • 1 mg
  • 5 mg

Y-27632

B1293-10 10 mg
EUR 142
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?.

Y-27632

B1293-200 200 mg
EUR 1070
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?.

Y-27632

B1293-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?.

Y-27632

B1293-50 50 mg
EUR 421
Description: Y-27632 is a specific inhibitor of Rho-associated kinases(ROCK) family with Ki values of 0.22?M and 0.30?M for ROCK1 and ROCK2, respectively.Y-27632 has shown selectivity of inhibition by comparing their Ki values for other Rho effector kinases, citron kinase and PKN, as well as PKC?.

EZSolution? Y-27632

1784-5
EUR 446

EZSolution? Y-27632, Sterile-Filtered

1994-1
EUR 359

Y 27632 (ROCK kinase inhibitor)

SIH-486-1MG 1 mg
EUR 149
Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble.

Y 27632 (ROCK kinase inhibitor)

SIH-486-5MG 5 mg
EUR 328
Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble.

Y-33075 (dihydrochloride)

HY-10069 5mg
EUR 215

Y-39983 dihydrochloride

B1176-10 10 mg
EUR 412
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1].

Y-39983 dihydrochloride

B1176-100 100 mg
EUR 2401
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1].

Y-39983 dihydrochloride

B1176-5 5 mg
EUR 267
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1].

Y-39983 dihydrochloride

B1176-50 50 mg
EUR 1497
Description: Y-39983 dihydrochloride is a novel and selective inhibitor of ROCK family with IC50 value of 3.6nM for ROCK [1].

SNRPF Polyclonal Antibody

27632-100ul 100ul
EUR 252

SNRPF Polyclonal Antibody

27632-50ul 50ul
EUR 187

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TBW01154 10mg Ask for price

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EUR 480

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EUR 166

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B2982-1 1 g
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2025-5
EUR 126

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2055-25
EUR 338

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EUR 126

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2362-250
EUR 414

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2362-50
EUR 142

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2520-100
EUR 131

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EUR 370

Antipain dihydrochloride

2834-25
EUR 327

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2834-5
EUR 120

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2835-25
EUR 588

Dorsmorphin dihydrochloride

2835-5
EUR 185

GGACK Dihydrochloride

1847-5 5 mg
EUR 319
Description: A potent and irreversible inhibitor of Urokinase (uPA (IC??<1 µM), Factor VIIa, Factor IXa, Factor Xa, and trypsin.

PPACK Dihydrochloride

1848-5
EUR 251

Puromycin Dihydrochloride

1860-100
EUR 272

Puromycin Dihydrochloride

1860-1000
EUR 1295

Puromycin Dihydrochloride

1860-25
EUR 126

Puromycin Dihydrochloride

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EUR 457

Puromycin Dihydrochloride

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EUR 805

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1970-250
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1970-50
EUR 137

Dexpramipexole dihydrochloride

B2215-25
EUR 457

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B2215-5
EUR 153

Daclatasvir dihydrochloride

B2224-25
EUR 414

Daclatasvir dihydrochloride

B2224-5
EUR 142

Netarsudil dihydrochloride

B2387-25
EUR 457

Netarsudil dihydrochloride

B2387-5
EUR 153

Furamidine dihydrochloride

B2581-25
EUR 544

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B2581-5
EUR 175

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HY-N2260 5mg
EUR 340

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HY-U00445 100mg
EUR 946

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EUR 160

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E005-100G 100 g
EUR 424

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E005-25G 25 g
EUR 143

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EUR 232

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C095-50MG 50 mg
EUR 144

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C157-25G 25 g
EUR 185

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C157-5G 5 g
EUR 72

Y-27632 dihydrochloride