Y-27632 dihydrochloride

Y-27632 dihydrochloride

To Order Now: info@anbioq.org

Y-27632 dihydrochloride
A3008-200	ApexBio	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	ApexBio	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	ApexBio	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	MedChemExpress	50mg	EUR 291

Y-27632 dihydrochloride
GK8578-1MG	Glentham Life Sciences	1 mg	EUR 142

Y-27632 dihydrochloride
GK8578-25MG	Glentham Life Sciences	25 mg	EUR 788

Y-27632 dihydrochloride
GK8578-5MG	Glentham Life Sciences	5 mg	EUR 333

Y-27632
B1293-10	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	Abbexa	EUR 272.00 EUR 523.00	1 mg 5 mg
Shipped within 5-12 working days.

Y-27632
E1KS1049	EnoGene	2 mg	EUR 325

Y-27632
HY-10071	MedChemExpress	100mg	EUR 1234

EZSolution? Y-27632
1784-5	Biovision		EUR 446

EZSolution? Y-27632, Sterile-Filtered
1994-1	Biovision		EUR 359

Y 27632 (ROCK kinase inhibitor)
SIH-486-1MG	Stressmarq	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	Stressmarq	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	MedChemExpress	5mg	EUR 215

SNRPF Polyclonal Antibody
27632-100ul	SAB	100ul	EUR 252

SNRPF Polyclonal Antibody
27632-50ul	SAB	50ul	EUR 187

Vatalanib Dihydrochloride
2025-25	Biovision		EUR 305

Vatalanib Dihydrochloride
2025-5	Biovision		EUR 126

1400W dihydrochloride
2055-25	Biovision		EUR 338

1400W dihydrochloride
2055-5	Biovision		EUR 126

Norquetiapine dihydrochloride
2362-250	Biovision		EUR 414

Norquetiapine dihydrochloride
2362-50	Biovision		EUR 142

Berbamine dihydrochloride
2520-100	Biovision		EUR 131

Berbamine dihydrochloride
2520-500	Biovision		EUR 370

Antipain dihydrochloride
2834-25	Biovision		EUR 327

Antipain dihydrochloride
2834-5	Biovision		EUR 120

Dorsmorphin dihydrochloride
2835-25	Biovision		EUR 588

Dorsmorphin dihydrochloride
2835-5	Biovision		EUR 185

GGACK Dihydrochloride
1847-5	Biovision	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	Biovision		EUR 251

Puromycin Dihydrochloride
1860-100	Biovision		EUR 272

Puromycin Dihydrochloride
1860-1000	Biovision		EUR 1295

Puromycin Dihydrochloride
1860-25	Biovision		EUR 126

Puromycin Dihydrochloride
1860-250	Biovision		EUR 457

Puromycin Dihydrochloride
1860-500	Biovision		EUR 805

Emetine dihydrochloride
1970-250	Biovision		EUR 359

Emetine dihydrochloride
1970-50	Biovision		EUR 137

Dexpramipexole dihydrochloride
B2215-25	Biovision		EUR 457

Dexpramipexole dihydrochloride
B2215-5	Biovision		EUR 153

Daclatasvir dihydrochloride
B2224-25	Biovision		EUR 414

Daclatasvir dihydrochloride
B2224-5	Biovision		EUR 142

Netarsudil dihydrochloride
B2387-25	Biovision		EUR 457

Netarsudil dihydrochloride
B2387-5	Biovision		EUR 153

Furamidine dihydrochloride
B2581-25	Biovision		EUR 544

Furamidine dihydrochloride
B2581-5	Biovision		EUR 175

Vanoxerine dihydrochloride
B3248-10	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	1 g	EUR 150
Description: Spectinomycin Dihydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.

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

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

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

Mizolastine dihydrochloride
B1116-100	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	10 mM (in 1mL DMSO)	EUR 108

Cystamine dihydrochloride
B5785-50	ApexBio	50 mg	EUR 112

Fluphenazine dihydrochloride
B6132-100	ApexBio	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	ApexBio	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	ApexBio	50 mg	EUR 268

Dimaprit dihydrochloride
B6328-100	ApexBio	100 mg	EUR 268

Naloxonazine dihydrochloride
B6366-10	ApexBio	10 mg	EUR 221

Naloxonazine dihydrochloride
B6366-50	ApexBio	50 mg	EUR 772

Ethambutol dihydrochloride
E005-100G	TOKU-E	100 g	EUR 424

Ethambutol dihydrochloride
E005-25G	TOKU-E	25 g	EUR 143

Piperazine Dihydrochloride
abx180858-100g	Abbexa	100 g	EUR 230
Shipped within 1-2 weeks.

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

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

DMPQ Dihydrochloride
20-abx076714	Abbexa	EUR 578.00 EUR 272.00	25 mg 5 mg
Shipped within 5-12 working days.

H89 Dihydrochloride
20-abx076747	Abbexa	EUR 676.00 EUR 300.00	25 mg 5 mg
Shipped within 5-12 working days.

Naftopidil Dihydrochloride
E1KS1387	EnoGene	25mg	EUR 247

Antipain, dihydrochloride
ADJ692	BBI Biotech	5mg	EUR 92.11
Product category: Biochemicals/Enzyme Inhibitors/Protease Inhibitors

Cefotiam Dihydrochloride
C095-100MG	TOKU-E	100 mg	EUR 232

Cefotiam Dihydrochloride
C095-50MG	TOKU-E	50 mg	EUR 144

Chlorhexidine Dihydrochloride
C157-25G	TOKU-E	25 g	EUR 185

Chlorhexidine Dihydrochloride
C157-5G	TOKU-E	5 g	EUR 72

Piribedil dihydrochloride
B6557-10	ApexBio	10 mg	EUR 139

Piribedil dihydrochloride
B6557-100	ApexBio	100 mg	EUR 215

Piribedil dihydrochloride
B6557-200	ApexBio	200 mg	EUR 337

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

Piribedil dihydrochloride
B6557-50	ApexBio	50 mg	EUR 186

Piribedil dihydrochloride
B6557-500	ApexBio	500 mg	EUR 563

Pirenzepine dihydrochloride
B6582-100	ApexBio	100 mg	EUR 134

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

Pirenzepine dihydrochloride
B6582-500	ApexBio	500 mg	EUR 183

Telenzepine dihydrochloride
B6606-10	ApexBio	10 mg	EUR 161

Telenzepine dihydrochloride
B6606-50	ApexBio	50 mg	EUR 480

DMPQ dihydrochloride
B6642-10	ApexBio	10 mg	EUR 186

DMPQ dihydrochloride
B6642-5	ApexBio	5 mg	EUR 154

GNTI dihydrochloride
B6669-10	ApexBio	10 mg	EUR 383

GNTI dihydrochloride
B6669-50	ApexBio	50 mg	EUR 1455

1400W dihydrochloride
B6730-10	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	10 mg	EUR 324

Rimcazole dihydrochloride
B6765-50	ApexBio	50 mg	EUR 1211

Zimelidine dihydrochloride
B6851-10	ApexBio	10 mg	EUR 177

Zimelidine dihydrochloride
B6851-50	ApexBio	50 mg	EUR 593

MPP dihydrochloride
B6910-10	ApexBio	10 mg	EUR 318

MPP dihydrochloride
B6910-50	ApexBio	50 mg	EUR 1178

Linopirdine dihydrochloride
B6916-10	ApexBio	10 mg	EUR 273

Linopirdine dihydrochloride
B6916-5	ApexBio	5 mg	EUR 187

Zoniporide dihydrochloride
B7160-10	ApexBio	10 mg	EUR 389

Zoniporide dihydrochloride
B7160-50	ApexBio	50 mg	EUR 1476

Flupenthixol dihydrochloride
B7578-50	ApexBio	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	ApexBio	10 mM (in 1mL H2O)	EUR 119
Description: Puromycin dihydrochloride [1] is an analog of aminoacyl-tRNA.

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

Veliparib dihydrochloride
A3958-10	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	10 mg	EUR 137
Description: IC50: N/ARetigabine is a first-in-class K+ channel (KCNQ) opener.

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

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

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

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

GGACK Dihydrochloride
A2582-5	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	ApexBio	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	MedChemExpress	10mM/1mL	EUR 141

Vatalanib (dihydrochloride)
HY-12018	MedChemExpress	100mg	EUR 201

AT7867 (dihydrochloride)
HY-12059A	MedChemExpress	100mg	EUR 1413

GSK369796 Dihydrochloride
HY-12082A	MedChemExpress	100mg	EUR 1566

GSK3368715 (dihydrochloride)
HY-128717A	MedChemExpress	10mM/1mL	EUR 549

Vanoxerine (dihydrochloride)
HY-13217	MedChemExpress	10mM/1mL	EUR 126

Dorsomorphin (dihydrochloride)
HY-13418	MedChemExpress	100mg	EUR 670

PF429242 (dihydrochloride)
HY-13447A	MedChemExpress	10mM/1mL	EUR 172

Mitoxantrone (dihydrochloride)
HY-13502A	MedChemExpress	50mg	EUR 119

Cutamesine dihydrochloride
HY-13510	MedChemExpress	10mM/1mL	EUR 230

Banoxantrone (dihydrochloride)
HY-13562A	MedChemExpress	10mg	EUR 243

Quinacrine (dihydrochloride)
HY-13735A	MedChemExpress	500mg	EUR 160

Sardomozide dihydrochloride
HY-13746B	MedChemExpress	10mM/1mL	EUR 226

Latrepirdine (dihydrochloride)
HY-14537	MedChemExpress	10mM/1mL	EUR 113

Inolitazone (dihydrochloride)
HY-14792B	MedChemExpress	5mg	EUR 544

Bavisant (dihydrochloride)
HY-14880A	MedChemExpress	5mg	EUR 326

Mirodenafil (dihydrochloride)
HY-14930A	MedChemExpress	50mg	EUR 2116

SCH79797 (dihydrochloride)
HY-14994	MedChemExpress	10mg	EUR 1175

Ipatasertib dihydrochloride
HY-15186A	MedChemExpress	50mg	EUR 383

GW791343 (dihydrochloride)
HY-15469	MedChemExpress	5mg	EUR 147

Merestinib dihydrochloride
HY-15514A	MedChemExpress	10mg	EUR 354

Mibefradil (dihydrochloride)
HY-15553A	MedChemExpress	10mg	EUR 259

Ceritinib dihydrochloride
HY-15656A	MedChemExpress	5mg	EUR 108

CRT0066101 dihydrochloride
HY-15698A	MedChemExpress	25mg	EUR 463

Flupentixol dihydrochloride
HY-15856B	MedChemExpress	10mg	EUR 131

TMB (dihydrochloride)
HY-15930A	MedChemExpress	10mM/1mL	EUR 113

Histamine dihydrochloride
HB0501	BBI Biotech	5g	EUR 60.44
Product category: Biochemicals/Amino Acids/Derivatives

Eravacycline (dihydrochloride)
HY-16980A	MedChemExpress	10mM/1mL	EUR 146

Pirenzepine (dihydrochloride)
HY-17037	MedChemExpress	500mg	EUR 160

Cetirizine (dihydrochloride)
HY-17042A	MedChemExpress	10mM/1mL	EUR 126

Pramipexole (dihydrochloride)
HY-17355	MedChemExpress	10mg	EUR 119

Dexpramipexole (dihydrochloride)
HY-17355A	MedChemExpress	10mg	EUR 153

Ranolazine (dihydrochloride)
HY-17401	MedChemExpress	10mM/1mL	EUR 156

Manidipine (dihydrochloride)
HY-17403	MedChemExpress	10mM/1mL	EUR 134

Prexasertib (dihydrochloride)
HY-18174A	MedChemExpress	100mg	EUR 1083

Azimilide (Dihydrochloride)
HY-18600A	MedChemExpress	100mg	EUR 1083

1400W (Dihydrochloride)
HY-18731	MedChemExpress	10mM/1mL	EUR 126

MS023 (dihydrochloride)
HY-19615B	MedChemExpress	100mg	EUR 911

DG172 (dihydrochloride)
HY-19737A	MedChemExpress	50mg	EUR 587

Elacestrant (dihydrochloride)
HY-19822A	MedChemExpress	10mM/1mL	EUR 613

Talipexole dihydrochloride
HY-A0008	MedChemExpress	10mM/1mL	EUR 179

Decloxizine (dihydrochloride)
HY-A0075	MedChemExpress	100mg	EUR 243

Fluphenazine (dihydrochloride)
HY-A0081	MedChemExpress	100mg	EUR 133

Sapropterin (dihydrochloride)
HY-A0124A	MedChemExpress	100mg	EUR 243

Y-27632 dihydrochloride