Y-27632 dihydrochloride 

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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

Telenzepine dihydrochloride

B6606-10 10 mg
EUR 161

Telenzepine dihydrochloride

B6606-50 50 mg
EUR 480

DMPQ dihydrochloride

B6642-10 10 mg
EUR 186

DMPQ dihydrochloride

B6642-5 5 mg
EUR 154

GNTI dihydrochloride

B6669-10 10 mg
EUR 383

GNTI dihydrochloride

B6669-50 50 mg
EUR 1455

1400W dihydrochloride

B6730-10 10 mg
EUR 142
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response.

1400W dihydrochloride

B6730-100 100 mg
EUR 728
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response.

1400W dihydrochloride

B6730-50 50 mg
EUR 438
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response.

Rimcazole dihydrochloride

B6765-10 10 mg
EUR 324

Rimcazole dihydrochloride

B6765-50 50 mg
EUR 1211

Zimelidine dihydrochloride

B6851-10 10 mg
EUR 177

Zimelidine dihydrochloride

B6851-50 50 mg
EUR 593

MPP dihydrochloride

B6910-10 10 mg
EUR 318

MPP dihydrochloride

B6910-50 50 mg
EUR 1178

Linopirdine dihydrochloride

B6916-10 10 mg
EUR 273

Linopirdine dihydrochloride

B6916-5 5 mg
EUR 187

Mizolastine dihydrochloride

B1116-100 100 mg
EUR 238
Description: Mizolastine dihydrochloride is a histamine H1-receptor antagonist with IC50 of 47 nM used in the treatment of hay fever (seasonal allergic rhinitis), hives and other allergic reactions.

Mizolastine dihydrochloride

B1116-200 200 mg
EUR 390
Description: Mizolastine dihydrochloride is a histamine H1-receptor antagonist with IC50 of 47 nM used in the treatment of hay fever (seasonal allergic rhinitis), hives and other allergic reactions.

Mizolastine dihydrochloride

B1116-500 500 mg
EUR 653
Description: Mizolastine dihydrochloride is a histamine H1-receptor antagonist with IC50 of 47 nM used in the treatment of hay fever (seasonal allergic rhinitis), hives and other allergic reactions.

Zoniporide dihydrochloride

B7160-10 10 mg
EUR 389

Zoniporide dihydrochloride

B7160-50 50 mg
EUR 1476

Flupenthixol dihydrochloride

B7578-50 50 mg
EUR 129
Description: MIC: 10-100 ?g/mL in most of the strainsFlupenthixol, introduced in 1965 by Lundbeck, marketed under brand names such asDepixol.Flupenthixolis atypical antipsychoticdrugof thethioxantheneclass.

Puromycin dihydrochloride

B7587-5.1 10 mM (in 1mL H2O)
EUR 119
Description: Puromycin dihydrochloride [1] is an analog of aminoacyl-tRNA.

Puromycin dihydrochloride

B7587-50 50 mg
EUR 131
Description: Puromycin dihydrochloride [1] is an analog of aminoacyl-tRNA.

Cefotiam Dihydrochloride

C095-100MG 100 mg
EUR 232

Cefotiam Dihydrochloride

C095-50MG 50 mg
EUR 144

Chlorhexidine Dihydrochloride

C157-25G 25 g
EUR 185

Chlorhexidine Dihydrochloride

C157-5G 5 g
EUR 72

Naftopidil Dihydrochloride

E1KS1387 25mg
EUR 247

MRT68921 (dihydrochloride)

HY-100006A 10mM/1mL
EUR 141

Dilazep (dihydrochloride)

HY-100957 10mM/1mL
EUR 196

ZK756326 (dihydrochloride)

HY-101038A 100mg
EUR 725

Veliparib (dihydrochloride)

HY-10130 200mg
EUR 766

PAβN (dihydrochloride)

HY-101444A 10mM/1mL
EUR 129

IT1t (dihydrochloride)

HY-101458A 10mg
EUR 257

Lesopitron (dihydrochloride)

HY-101609 20mg
EUR 2530

UAMC00039 (dihydrochloride)

HY-101769 10mM/1mL
EUR 166

Tirbanibulin (dihydrochloride)

HY-10340A 50mg
EUR 698

LCL521 dihydrochloride

HY-103593A 10mg
EUR 681

Canertinib (dihydrochloride)

HY-10367A 10mM/1mL
EUR 126

Daclatasvir (dihydrochloride)

HY-10465 100mg
EUR 153

JDTic (dihydrochloride)

HY-10487 50mg
EUR 1251

Lexibulin (dihydrochloride)

HY-10498A 5mg
EUR 181

Liarozole (dihydrochloride)

HY-106019C 1mg
EUR 160

Nolatrexed dihydrochloride

HY-108474 10mM/1mL
EUR 138

Dianicline (dihydrochloride)

HY-110241 1mg
EUR 124

Flupentixol dihydrochloride

HY-15856B 10mg
EUR 131

TMB (dihydrochloride)

HY-15930A 10mM/1mL
EUR 113

Eravacycline (dihydrochloride)

HY-16980A 10mM/1mL
EUR 146

Pirenzepine (dihydrochloride)

HY-17037 500mg
EUR 160

Cetirizine (dihydrochloride)

HY-17042A 10mM/1mL
EUR 126

Pramipexole (dihydrochloride)

HY-17355 10mg
EUR 119

Dexpramipexole (dihydrochloride)

HY-17355A 10mg
EUR 153

Ranolazine (dihydrochloride)

HY-17401 10mM/1mL
EUR 156

Manidipine (dihydrochloride)

HY-17403 10mM/1mL
EUR 134

Prexasertib (dihydrochloride)

HY-18174A 100mg
EUR 1083

Azimilide (Dihydrochloride)

HY-18600A 100mg
EUR 1083

1400W (Dihydrochloride)

HY-18731 10mM/1mL
EUR 126

MS023 (dihydrochloride)

HY-19615B 100mg
EUR 911

DG172 (dihydrochloride)

HY-19737A 50mg
EUR 587

Elacestrant (dihydrochloride)

HY-19822A 10mM/1mL
EUR 613

Talipexole dihydrochloride

HY-A0008 10mM/1mL
EUR 179

Y-27632 dihydrochloride