Y-27632 dihydrochloride 

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Y-27632 dihydrochloride
GK8578-25MG 25 mg
EUR 788

Y-27632 dihydrochloride
GK8578-5MG 5 mg
EUR 333

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, dihydrochloride
1596-1
EUR 175

Y-27632, dihydrochloride
1596-5
EUR 463

Y-27632, dihydrochloride
1596-50
EUR 2469

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?.

Y-27632
E1KS1049 2 mg
EUR 325

Y-27632
HY-10071 100mg
EUR 1234

Y 27632
20-abx076548
  • EUR 272.00
  • EUR 523.00
  • 1 mg
  • 5 mg
  • Shipped within 5-12 working days.

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
  • Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
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
  • Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
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-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].

Y-33075 (dihydrochloride)
HY-10069 5mg
EUR 215

SNRPF Polyclonal Antibody
27632-100ul 100ul
EUR 252

SNRPF Polyclonal Antibody
27632-50ul 50ul
EUR 187

Dexpramipexole dihydrochloride
B2215-25
EUR 457

Dexpramipexole dihydrochloride
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

Furamidine dihydrochloride
B2581-5
EUR 175

Vanoxerine dihydrochloride
B3248-10 10 mg
EUR 118
Description: Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases.

Vanoxerine dihydrochloride
B3248-25 25 mg
EUR 210
Description: Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases.

Vanoxerine dihydrochloride
B3248-50 50 mg
EUR 332
Description: Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases.

Spectinomycin dihydrochloride
B3342-1000 1 g
EUR 150
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

Spectinomycin dihydrochloride
B3342-5.1 10 mM (in 1mL H2O)
EUR 168
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

Spectinomycin dihydrochloride
B3342-5000 5 g
EUR 283
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

Pentamidine dihydrochloride
B3416-50 50 mg
EUR 128
Description: Pentamidine Dihydrochloride(MP601205 dihydrochloride) is an antimicrobial agent.

IT1t dihydrochloride
B5650-10 10 mg
EUR 321
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12.

IT1t dihydrochloride
B5650-100 100 mg
EUR 1750
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12.

IT1t dihydrochloride
B5650-25 25 mg
EUR 592
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12.

IT1t dihydrochloride
B5650-5 5 mg
EUR 203
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12.

IT1t dihydrochloride
B5650-5.1 10 mM (in 1mL DMSO)
EUR 218
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12.

IT1t dihydrochloride
B5650-50 50 mg
EUR 1027
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12.

Cystamine dihydrochloride
B5785-5.1 10 mM (in 1mL DMSO)
EUR 108

Cystamine dihydrochloride
B5785-50 50 mg
EUR 112

Fluphenazine dihydrochloride
B6132-100 100 mg
EUR 150
Description: EC50: 1.24 ?MFluphenazine is a dopamine D1 and D2 receptor inhibitor.Dopamine D1 and D2 receptor immunohistochemistry has been used to study the structure of the adult rat arcuate-median eminence complex, particularly in relation to the tubero-infundibular dopamine neurons.

Fluphenazine dihydrochloride
B6132-5.1 10 mM (in 1mL DMSO)
EUR 168
Description: EC50: 1.24 ?MFluphenazine is a dopamine D1 and D2 receptor inhibitor.Dopamine D1 and D2 receptor immunohistochemistry has been used to study the structure of the adult rat arcuate-median eminence complex, particularly in relation to the tubero-infundibular dopamine neurons.

Dilazep dihydrochloride
B6316-50 50 mg
EUR 268

Dimaprit dihydrochloride
B6328-100 100 mg
EUR 268

Naloxonazine dihydrochloride
B6366-10 10 mg
EUR 221

Naloxonazine dihydrochloride
B6366-50 50 mg
EUR 772

Piribedil dihydrochloride
B6557-10 10 mg
EUR 139

Piribedil dihydrochloride
B6557-100 100 mg
EUR 215

Piribedil dihydrochloride
B6557-200 200 mg
EUR 337

Piribedil dihydrochloride
B6557-5.1 10 mM (in 1mL DMSO)
EUR 150

Piribedil dihydrochloride
B6557-50 50 mg
EUR 186

Piribedil dihydrochloride
B6557-500 500 mg
EUR 563

Pirenzepine dihydrochloride
B6582-100 100 mg
EUR 134

Pirenzepine dihydrochloride
B6582-5.1 10 mM (in 1mL DMSO)
EUR 150

Pirenzepine dihydrochloride
B6582-500 500 mg
EUR 183

Y-27632 dihydrochloride