Y-27632 dihydrochloride

Y-27632 dihydrochloride

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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)

HY-10583 50mg
EUR 291

Y-27632 dihydrochloride

GK8578-1MG 1 mg
EUR 142

Y-27632 dihydrochloride

GK8578-25MG 25 mg
EUR 788

Y-27632 dihydrochloride

GK8578-5MG 5 mg
EUR 333

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

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

Y-27632

E1KS1049 2 mg
EUR 325

Y-27632

HY-10071 100mg
EUR 1234

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

Vatalanib Dihydrochloride

2025-25
EUR 305

Vatalanib Dihydrochloride

2025-5
EUR 126

1400W dihydrochloride

2055-25
EUR 338

1400W dihydrochloride

2055-5
EUR 126

Norquetiapine dihydrochloride

2362-250
EUR 414

Norquetiapine dihydrochloride

2362-50
EUR 142

Berbamine dihydrochloride

2520-100
EUR 131

Berbamine dihydrochloride

2520-500
EUR 370

Antipain dihydrochloride

2834-25
EUR 327

Antipain dihydrochloride

2834-5
EUR 120

Dorsmorphin dihydrochloride

2835-25
EUR 588

Dorsmorphin dihydrochloride

2835-5
EUR 185

GGACK Dihydrochloride

1847-5 5 mg
EUR 319
  • Frequently asked questions for this product: Is the GGACK Dihydrochloride cell-permeable? - No
  • Is this item a salt form of GGACK Dihydrochloride? - Yes
  • Does this product have/require an MSDS? - Yes
  • What is the biological function of this molecul
  • Show more
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

1860-250
EUR 457

Puromycin Dihydrochloride

1860-500
EUR 805

Emetine dihydrochloride

1970-250
EUR 359

Emetine dihydrochloride

1970-50
EUR 137

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.

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.

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

Ethambutol dihydrochloride

E005-100G 100 g
EUR 424

Ethambutol dihydrochloride

E005-25G 25 g
EUR 143

Piperazine Dihydrochloride

abx180858-100g 100 g
EUR 230
  • Shipped within 1-2 weeks.

Pramipexole dihydrochloride

20-abx180860
  • EUR 453.00
  • EUR 230.00
  • EUR 370.00
  • 10 g
  • 1 g
  • 5 g
  • Shipped within 1-2 weeks.

Vatalanib Dihydrochloride

20-abx076544
  • EUR 258.00
  • EUR 495.00
  • 10 mg
  • 50 mg
  • Shipped within 5-12 working days.

DMPQ Dihydrochloride

20-abx076714
  • EUR 578.00
  • EUR 272.00
  • 25 mg
  • 5 mg
  • Shipped within 5-12 working days.

H89 Dihydrochloride

20-abx076747
  • EUR 676.00
  • EUR 300.00
  • 25 mg
  • 5 mg
  • Shipped within 5-12 working days.

Naftopidil Dihydrochloride

E1KS1387 25mg
EUR 247

Antipain, dihydrochloride

ADJ692 5mg
EUR 92.11
  • Product category: Biochemicals/Enzyme Inhibitors/Protease Inhibitors

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

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

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.

Veliparib dihydrochloride

A3958-10 10 mg
EUR 148
Description: Veliparib dihydrochloride is a potent inhibitor of PARP-1 and PARP-2 with K (i) s of 5.2 and 2.9 nmol/L, respectively [1].PARP is short of poly ADP ribose polymerase and is reported as an overexpressed enzyme in a variety of cancers.

Veliparib dihydrochloride

A3958-200 200 mg
EUR 835
Description: Veliparib dihydrochloride is a potent inhibitor of PARP-1 and PARP-2 with K (i) s of 5.2 and 2.9 nmol/L, respectively [1].PARP is short of poly ADP ribose polymerase and is reported as an overexpressed enzyme in a variety of cancers.

Veliparib dihydrochloride

A3958-5 5 mg
EUR 125
Description: Veliparib dihydrochloride is a potent inhibitor of PARP-1 and PARP-2 with K (i) s of 5.2 and 2.9 nmol/L, respectively [1].PARP is short of poly ADP ribose polymerase and is reported as an overexpressed enzyme in a variety of cancers.

Veliparib dihydrochloride

A3958-5.1 10 mM (in 1mL DMSO)
EUR 116
Description: Veliparib dihydrochloride is a potent inhibitor of PARP-1 and PARP-2 with K (i) s of 5.2 and 2.9 nmol/L, respectively [1].PARP is short of poly ADP ribose polymerase and is reported as an overexpressed enzyme in a variety of cancers.

Veliparib dihydrochloride

A3958-50 50 mg
EUR 351
Description: Veliparib dihydrochloride is a potent inhibitor of PARP-1 and PARP-2 with K (i) s of 5.2 and 2.9 nmol/L, respectively [1].PARP is short of poly ADP ribose polymerase and is reported as an overexpressed enzyme in a variety of cancers.

AT7867 dihydrochloride

A3199-10 10 mg
EUR 340
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics.

AT7867 dihydrochloride

A3199-100 100 mg
EUR 1842
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics.

AT7867 dihydrochloride

A3199-5 5 mg
EUR 267
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics.

AT7867 dihydrochloride

A3199-5.1 10 mM (in 1mL DMSO)
EUR 287
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics.

AT7867 dihydrochloride

A3199-50 50 mg
EUR 1281
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics.

Canertinib dihydrochloride

A3276-10 10 mg
EUR 108
Description: Canertinib dihydrochloride is a selective inhibitor of Pan-erbB tyrosine kinase with IC50 value of 3.5 nM [1].ErbB receptor family is a member of the receptor tyrosine kinase superfamily and plays an important role in the normal breast development.

Canertinib dihydrochloride

A3276-100 100 mg
EUR 189
Description: Canertinib dihydrochloride is a selective inhibitor of Pan-erbB tyrosine kinase with IC50 value of 3.5 nM [1].ErbB receptor family is a member of the receptor tyrosine kinase superfamily and plays an important role in the normal breast development.

Canertinib dihydrochloride

A3276-50 50 mg
EUR 148
Description: Canertinib dihydrochloride is a selective inhibitor of Pan-erbB tyrosine kinase with IC50 value of 3.5 nM [1].ErbB receptor family is a member of the receptor tyrosine kinase superfamily and plays an important role in the normal breast development.

Inolitazone dihydrochloride

A3499-5 5 mg
EUR 698
Description: Description:IC50 Value: 0.8 nM [1]Inolitazone(RS5444) is a novel high-affinity PPARgamma agonist, which activates PPARgamma with an EC50 about 1/50th that of rosiglitazone and has no effect on RIE cells that do not express PPARgamma.

LDK378 dihydrochloride

A3544-10 10 mg
EUR 155
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM.

LDK378 dihydrochloride

A3544-100 100 mg
EUR 276
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM.

LDK378 dihydrochloride

A3544-5 5 mg
EUR 125
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM.

LDK378 dihydrochloride

A3544-5.1 10 mM (in 1mL H2O)
EUR 154
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM.

LDK378 dihydrochloride

A3544-50 50 mg
EUR 200
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM.

Mibefradil dihydrochloride

A3605-10 10 mg
EUR 263
Description: Mibefradil is calcium channel blocker with moderate selectivity for T-type Ca2+ channels displaying IC50 values of 2.7 ?M and 18.6 ?M for T-type and L-type channels respectively. Mibefradil is antihypertensive agent for the treatment of hypertension and chronic angina pectoris.

Mibefradil dihydrochloride

A3605-25 25 mg
EUR 553
Description: Mibefradil is calcium channel blocker with moderate selectivity for T-type Ca2+ channels displaying IC50 values of 2.7 ?M and 18.6 ?M for T-type and L-type channels respectively. Mibefradil is antihypertensive agent for the treatment of hypertension and chronic angina pectoris.

Mibefradil dihydrochloride

A3605-5 5 mg
EUR 168
Description: Mibefradil is calcium channel blocker with moderate selectivity for T-type Ca2+ channels displaying IC50 values of 2.7 ?M and 18.6 ?M for T-type and L-type channels respectively. Mibefradil is antihypertensive agent for the treatment of hypertension and chronic angina pectoris.

Mibefradil dihydrochloride

A3605-50 50 mg
EUR 996
Description: Mibefradil is calcium channel blocker with moderate selectivity for T-type Ca2+ channels displaying IC50 values of 2.7 ?M and 18.6 ?M for T-type and L-type channels respectively. Mibefradil is antihypertensive agent for the treatment of hypertension and chronic angina pectoris.

Pramipexole dihydrochloride

A3733-20 20 mg
EUR 108
Description: Pramipexole dihydrochloride is a dopamine receptor agonist with selectivity for the D3 receptor (Ki values are 3.9, 3.3, 0.5 and 3.9 nM for D2L, D2S, D3 and D4 receptors respectively). Pramipexole dihydrochloride exhibits negligable affinity for D1 and D5 receptors.

Pramipexole dihydrochloride

A3733-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: Pramipexole dihydrochloride is a dopamine receptor agonist with selectivity for the D3 receptor (Ki values are 3.9, 3.3, 0.5 and 3.9 nM for D2L, D2S, D3 and D4 receptors respectively). Pramipexole dihydrochloride exhibits negligable affinity for D1 and D5 receptors.

Pramipexole dihydrochloride

A3733-50 50 mg
EUR 131
Description: Pramipexole dihydrochloride is a dopamine receptor agonist with selectivity for the D3 receptor (Ki values are 3.9, 3.3, 0.5 and 3.9 nM for D2L, D2S, D3 and D4 receptors respectively). Pramipexole dihydrochloride exhibits negligable affinity for D1 and D5 receptors.

Retigabine dihydrochloride

A3758-10 10 mg
EUR 137
Description: IC50: N/ARetigabine is a first-in-class K+ channel (KCNQ) opener.

Retigabine dihydrochloride

A3758-100 100 mg
EUR 435
Description: IC50: N/ARetigabine is a first-in-class K+ channel (KCNQ) opener.

Retigabine dihydrochloride

A3758-5 5 mg
EUR 105
Description: IC50: N/ARetigabine is a first-in-class K+ channel (KCNQ) opener.

Retigabine dihydrochloride

A3758-5.1 10 mM (in 1mL DMSO)
EUR 142
Description: IC50: N/ARetigabine is a first-in-class K+ channel (KCNQ) opener.

Retigabine dihydrochloride

A3758-50 50 mg
EUR 271
Description: IC50: N/ARetigabine is a first-in-class K+ channel (KCNQ) opener.

GGACK Dihydrochloride

A2582-5 5 mg
EUR 235
Description: A potent and irreversible inhibitor of Urokinase (uPA (IC??<1 µM), Factor VIIa, Factor IXa, Factor Xa, and trypsin.

PPACK Dihydrochloride

A2588-10 10 mg
EUR 353
Description: PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective and irreversible inhibitor of thrombin that inhibits human ?-thrombin with inhibition constant Kivalue of 0.24 nM.

PPACK Dihydrochloride

A2588-25 25 mg
EUR 757
Description: PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective and irreversible inhibitor of thrombin that inhibits human ?-thrombin with inhibition constant Kivalue of 0.24 nM.

PPACK Dihydrochloride

A2588-5 5 mg
EUR 221
Description: PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective and irreversible inhibitor of thrombin that inhibits human ?-thrombin with inhibition constant Kivalue of 0.24 nM.

Alexidine dihydrochloride

A4542-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Selective inhibitor of protein tyrosine phosphatases localized to mitochondrion 1 (PTPMT1) (IC50 = 1.08 ?M in vitro). Stimulates increased insulin secretion by ?-cells in rat pancreatic islets. Displays antitcancer properties in FaDu cells.

Alexidine dihydrochloride

A4542-50 50 mg
EUR 184
Description: Selective inhibitor of protein tyrosine phosphatases localized to mitochondrion 1 (PTPMT1) (IC50 = 1.08 ?M in vitro). Stimulates increased insulin secretion by ?-cells in rat pancreatic islets. Displays antitcancer properties in FaDu cells.

MRT68921 (dihydrochloride)

HY-100006A 10mM/1mL
EUR 141

Vatalanib (dihydrochloride)

HY-12018 100mg
EUR 201

AT7867 (dihydrochloride)

HY-12059A 100mg
EUR 1413

GSK369796 Dihydrochloride

HY-12082A 100mg
EUR 1566

GSK3368715 (dihydrochloride)

HY-128717A 10mM/1mL
EUR 549

Vanoxerine (dihydrochloride)

HY-13217 10mM/1mL
EUR 126

Dorsomorphin (dihydrochloride)

HY-13418 100mg
EUR 670

PF429242 (dihydrochloride)

HY-13447A 10mM/1mL
EUR 172

Mitoxantrone (dihydrochloride)

HY-13502A 50mg
EUR 119

Cutamesine dihydrochloride

HY-13510 10mM/1mL
EUR 230

Banoxantrone (dihydrochloride)

HY-13562A 10mg
EUR 243

Quinacrine (dihydrochloride)

HY-13735A 500mg
EUR 160

Sardomozide dihydrochloride

HY-13746B 10mM/1mL
EUR 226

Latrepirdine (dihydrochloride)

HY-14537 10mM/1mL
EUR 113

Inolitazone (dihydrochloride)

HY-14792B 5mg
EUR 544

Bavisant (dihydrochloride)

HY-14880A 5mg
EUR 326

Mirodenafil (dihydrochloride)

HY-14930A 50mg
EUR 2116

SCH79797 (dihydrochloride)

HY-14994 10mg
EUR 1175

Ipatasertib dihydrochloride

HY-15186A 50mg
EUR 383

GW791343 (dihydrochloride)

HY-15469 5mg
EUR 147

Merestinib dihydrochloride

HY-15514A 10mg
EUR 354

Mibefradil (dihydrochloride)

HY-15553A 10mg
EUR 259

Ceritinib dihydrochloride

HY-15656A 5mg
EUR 108

CRT0066101 dihydrochloride

HY-15698A 25mg
EUR 463

Flupentixol dihydrochloride

HY-15856B 10mg
EUR 131

TMB (dihydrochloride)

HY-15930A 10mM/1mL
EUR 113

Histamine dihydrochloride

HB0501 5g
EUR 60.44
  • Product category: Biochemicals/Amino Acids/Derivatives

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

Decloxizine (dihydrochloride)

HY-A0075 100mg
EUR 243

Fluphenazine (dihydrochloride)

HY-A0081 100mg
EUR 133

Sapropterin (dihydrochloride)

HY-A0124A 100mg
EUR 243

Y-27632 dihydrochloride