PPACK Dihydrochloride 

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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.

PPACK II, trifluoroacetate
B2151-5
EUR 294

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.

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

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.

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

PPACK Dihydrochloride