Rauwolscine (hydrochloride)

HY-12710A 10mM/1mL
EUR 126

Gemcitabine HCl

A1402-100 100 mg
EUR 108
Description: Gemcitabine HCl is an inhibitor of DNA synthesis with the IC50 value of 240.4±29.0 ?M (CCRF-CEM/dCK-/- cells), 14.7±2.8 nM (TC-1 cells), 36.7 ± 5.1 ?M (TC-1-GR cells), and 50 nM (PANC1 cells).

Gemcitabine HCl

A1402-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Gemcitabine HCl is an inhibitor of DNA synthesis with the IC50 value of 240.4±29.0 ?M (CCRF-CEM/dCK-/- cells), 14.7±2.8 nM (TC-1 cells), 36.7 ± 5.1 ?M (TC-1-GR cells), and 50 nM (PANC1 cells).

Granisetron HCl

A1295-100 100 mg
EUR 189
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Granisetron HCl

A1295-5 5 mg
EUR 108
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Granisetron HCl

A1295-5.1 10 mM (in 1mL DMSO)
EUR 119
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Granisetron HCl

A1295-50 50 mg
EUR 131
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Metomidate HCL

50R-R7315 50 mg
EUR 176
Description: Metomidate HCL chemical reference substance

Raloxifene HCl

B1515-100 100 mg
EUR 142
Description: Raloxifene HCl?LY139481?is a potent and selective of estrogen receptor (ER) with the IC50 value of 2.9~5.7nM [1].Raloxifene HCl?LY139481?is a selective and uncompetitive of estrogen receptor (ER) with the IC50 value of 2.9~5.7nM for phthalazine oxidase in human liver cytosol

Raloxifene HCl

B1515-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: Raloxifene HCl?LY139481?is a potent and selective of estrogen receptor (ER) with the IC50 value of 2.9~5.7nM [1].Raloxifene HCl?LY139481?is a selective and uncompetitive of estrogen receptor (ER) with the IC50 value of 2.9~5.7nM for phthalazine oxidase in human liver cytosol

Raloxifene HCl

B1515-50 50 mg
EUR 108
Description: Raloxifene HCl?LY139481?is a potent and selective of estrogen receptor (ER) with the IC50 value of 2.9~5.7nM [1].Raloxifene HCl?LY139481?is a selective and uncompetitive of estrogen receptor (ER) with the IC50 value of 2.9~5.7nM for phthalazine oxidase in human liver cytosol

Bazedoxifene HCl

B1519-10 10 mg
EUR 622
Description: Bazedoxifene HCl is a novel, non-steroidal and indole-based estrogen receptor modulator (SERM). The IC50 value of bazedoxifene against ER? and ER? is 23 nM and 89 nM, respectively [1,2]. The estrogen receptor (ER) contains two subtypes, ER? and ER?.

Bazedoxifene HCl

B1519-5.1 10 mM (in 1mL DMSO)
EUR 502
Description: Bazedoxifene HCl is a novel, non-steroidal and indole-based estrogen receptor modulator (SERM). The IC50 value of bazedoxifene against ER? and ER? is 23 nM and 89 nM, respectively [1,2]. The estrogen receptor (ER) contains two subtypes, ER? and ER?.

Gabapentin HCl

B1529-100 100 mg
EUR 224
Description: Gabapentin (Neurontin) is a pharmaceutical drug, specifically a GABA analog. It was originally developed to treatepilepsy, and currently is also used to relieve neuropathic pain.

Gabapentin HCl

B1529-20 20 mg
EUR 108
Description: Gabapentin (Neurontin) is a pharmaceutical drug, specifically a GABA analog. It was originally developed to treatepilepsy, and currently is also used to relieve neuropathic pain.

Gabapentin HCl

B1529-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Gabapentin (Neurontin) is a pharmaceutical drug, specifically a GABA analog. It was originally developed to treatepilepsy, and currently is also used to relieve neuropathic pain.

Buclizine HCl

B1546-50 50 mg
EUR 128
Description: Buclizine HCL is an antihistamine and anticholinergic of the piperazine derivative family.

Tripelennamine HCl

B1553-100 100 mg
EUR 177
Description: Tripelennamine Hcl, a H1-receptor antagonist, is a psychoactive drug and member of the pyridine andethylenediamine classes that is used as an antipruritic and first-generation antihistamine.

Tripelennamine HCl

B1553-50 50 mg
EUR 131
Description: Tripelennamine Hcl, a H1-receptor antagonist, is a psychoactive drug and member of the pyridine andethylenediamine classes that is used as an antipruritic and first-generation antihistamine.

Azelastine HCl

B1568-100 100 mg
EUR 96
Description: Azelastine HCl is a potent, second-generation, selective, histamine antagonist.

Azelastine HCl

B1568-200 200 mg
EUR 108
Description: Azelastine HCl is a potent, second-generation, selective, histamine antagonist.

Azelastine HCl

B1568-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Azelastine HCl is a potent, second-generation, selective, histamine antagonist.

Azelastine HCl

B1568-S Evaluation Sample
EUR 81
Description: Azelastine HCl is a potent, second-generation, selective, histamine antagonist.

Fexofenadine HCl

B1573-10 10 mg
EUR 108
Description: Fexofenadine inhibits histamine H1 receptor with IC50 of 246 nM.

Fexofenadine HCl

B1573-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Fexofenadine inhibits histamine H1 receptor with IC50 of 246 nM.

Fexofenadine HCl

B1573-50 50 mg
EUR 189
Description: Fexofenadine inhibits histamine H1 receptor with IC50 of 246 nM.

Fexofenadine HCl

B1573-S Evaluation Sample
EUR 81
Description: Fexofenadine inhibits histamine H1 receptor with IC50 of 246 nM.

Olopatadine HCl

B1576-10 10 mg
EUR 128
Description: Olopatadine HCl is a histamine blocker used to treat allergic conjunctivitis.Olopatadine is one of the second-generation histamine H1 receptor antagonists that are treated for allergic disorders. Olopatadine significantly inhibited the ear swelling and th

Olopatadine HCl

B1576-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Olopatadine HCl is a histamine blocker used to treat allergic conjunctivitis.Olopatadine is one of the second-generation histamine H1 receptor antagonists that are treated for allergic disorders. Olopatadine significantly inhibited the ear swelling and th

Olopatadine HCl

B1576-50 50 mg
EUR 187
Description: Olopatadine HCl is a histamine blocker used to treat allergic conjunctivitis.Olopatadine is one of the second-generation histamine H1 receptor antagonists that are treated for allergic disorders. Olopatadine significantly inhibited the ear swelling and th

Olopatadine HCl

B1576-S Evaluation Sample
EUR 81
Description: Olopatadine HCl is a histamine blocker used to treat allergic conjunctivitis.Olopatadine is one of the second-generation histamine H1 receptor antagonists that are treated for allergic disorders. Olopatadine significantly inhibited the ear swelling and th

EPZ004777 HCl

B1581-5 5 mg
EUR 177
Description: EPZ004777 is a potent and selective inhibitor of DOT1L, a protein methyltransferase catalyzing the methylation of lysine 4 of histone H3 (H3K4), with the half maximal inhibition concentration IC50 value of 400 pM [1].

EPZ004777 HCl

B1581-50 50 mg
EUR 688
Description: EPZ004777 is a potent and selective inhibitor of DOT1L, a protein methyltransferase catalyzing the methylation of lysine 4 of histone H3 (H3K4), with the half maximal inhibition concentration IC50 value of 400 pM [1].

Biperiden HCl

B1598-100 100 mg
EUR 413
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Biperiden HCl

B1598-25 25 mg
EUR 147
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Biperiden HCl

B1598-5.1 10 mM (in 1mL DMSO)
EUR 154
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Biperiden HCl

B1598-500 500 mg
EUR 717
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Donepezil HCl

B1602-1000 1 g
EUR 135
Description: Donepezil Hydrochloride (Donepezil HCL) is a novel, potent and selective inhibitor of acetylcholinesterase (AChE), an enzyme possibly involved in cognitive dysfunction of patients suffering Alzheimer?s disease (AD), with the half maximal inhibition concentration IC50 value of 6.7 nM [1].

Donepezil HCl

B1602-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: Donepezil Hydrochloride (Donepezil HCL) is a novel, potent and selective inhibitor of acetylcholinesterase (AChE), an enzyme possibly involved in cognitive dysfunction of patients suffering Alzheimer?s disease (AD), with the half maximal inhibition concentration IC50 value of 6.7 nM [1].

Donepezil HCl

B1602-5000 5 g
EUR 309
Description: Donepezil Hydrochloride (Donepezil HCL) is a novel, potent and selective inhibitor of acetylcholinesterase (AChE), an enzyme possibly involved in cognitive dysfunction of patients suffering Alzheimer?s disease (AD), with the half maximal inhibition concentration IC50 value of 6.7 nM [1].

Alizapride HCl

B1653-100 100 mg
EUR 142
Description: Alizapride HCl

Alizapride HCl

B1653-1000 1 g
EUR 564
Description: Alizapride HCl

Alizapride HCl

B1653-250 250 mg
EUR 255
Description: Alizapride HCl

Amprolium HCl

B1663-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Amprolium chloride is a thiamin antagonist, which prevents carbohydrate synthesis by blocking thiamine uptake.

Amprolium HCl

B1663-50 50 mg
EUR 128
Description: Amprolium chloride is a thiamin antagonist, which prevents carbohydrate synthesis by blocking thiamine uptake.

Antazoline HCl

B1664-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Antazoline HCl is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine.

Antazoline HCl

B1664-50 50 mg
EUR 128
Description: Antazoline HCl is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine.

Benzydamine HCl

B1677-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Benzydamine hydrochloride is a topical nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, antipyretic and local anesthetic activity.

Benzydamine HCl

B1677-50 50 mg
EUR 128
Description: Benzydamine hydrochloride is a topical nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, antipyretic and local anesthetic activity.

Buspirone HCl

B1687-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Buspirone HCl

Buspirone HCl

B1687-50 50 mg
EUR 128
Description: Buspirone HCl

Chlorhexidine HCl

B1695-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Chlorhexidine hydrochloride is an antiseptic effective against a wide variety of gram-negative and gram-positive organisms.

Chlorhexidine HCl

B1695-50 50 mg
EUR 128
Description: Chlorhexidine hydrochloride is an antiseptic effective against a wide variety of gram-negative and gram-positive organisms.

Chlortetracycline HCl

B1699-250 250 mg
EUR 134
Description: Chlortetracycline HCl is the first identified tetracycline antibiotic.

Chlortetracycline HCl

B1699-5.1 10 mM (in 1mL H2O)
EUR 150
Description: Chlortetracycline HCl is the first identified tetracycline antibiotic.

Clorprenaline HCL

B1713-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Clorprenaline HCl is a ?2-receptor agonist, it has a significant expansion of the bronchial effect.

Clorprenaline HCL

B1713-50 50 mg
EUR 128
Description: Clorprenaline HCl is a ?2-receptor agonist, it has a significant expansion of the bronchial effect.

Cysteamine HCl

B1719-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Cysteamine is an agent for the treatment of nephropathic cystinosis and an antioxidant.

Cysteamine HCl

B1719-50 50 mg
EUR 128
Description: Cysteamine is an agent for the treatment of nephropathic cystinosis and an antioxidant.

Epinastine HCl

B1744-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Epinastine is an antihistamine and mast cell stabilizer that is used in eye drops to treat allergic conjunctivitis.

Epinastine HCl

B1744-50 50 mg
EUR 128
Description: Epinastine is an antihistamine and mast cell stabilizer that is used in eye drops to treat allergic conjunctivitis.

Esmolol HCl

B1748-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Esmolol is a cardioselective b-blocker, used to control rapid heartbeats or abnormal heart rhythms.

Esmolol HCl

B1748-50 50 mg
EUR 128
Description: Esmolol is a cardioselective b-blocker, used to control rapid heartbeats or abnormal heart rhythms.

Fenspiride HCl

B1754-25000 25 g
EUR 255
Description: Fenspiride Hcl is an ? adrenergic and H1 histamine receptor antagonist.

Fenspiride HCl

B1754-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: Fenspiride Hcl is an ? adrenergic and H1 histamine receptor antagonist.

Fenspiride HCl

B1754-5000 5 g
EUR 134
Description: Fenspiride Hcl is an ? adrenergic and H1 histamine receptor antagonist.

Furaltadone HCl

B1764-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Furaltadone HCl is an antibacterial and has distinct curative effect in the treatment of coccidiosis.

Furaltadone HCl

B1764-50 50 mg
EUR 128
Description: Furaltadone HCl is an antibacterial and has distinct curative effect in the treatment of coccidiosis.

Levobetaxolol HCl

B1778-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Levobetaxolol exhibits a higher affinity at cloned human ?1 and ?2 receptors with Ki value of 0.76 nM and 32.6 nM, respectively.

Levobetaxolol HCl

B1778-50 50 mg
EUR 128
Description: Levobetaxolol exhibits a higher affinity at cloned human ?1 and ?2 receptors with Ki value of 0.76 nM and 32.6 nM, respectively.

Lomefloxacin HCl

B1781-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Lomefloxacin HCl is a fluoroquinolone antibiotic.

Lomefloxacin HCl

B1781-50 50 mg
EUR 128
Description: Lomefloxacin HCl is a fluoroquinolone antibiotic.

Lomerizine HCl

B1782-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Lomerizine dihydrochloride is a relatively new L- and T-type calcium channel blocker used in the treatment of migraine.

Lomerizine HCl

B1782-50 50 mg
EUR 128
Description: Lomerizine dihydrochloride is a relatively new L- and T-type calcium channel blocker used in the treatment of migraine.

Levobupivacaine HCl

B1784-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Levobupivacaine HCl, the pure S(-)-enantiomer of bupivacaine, is a long-acting local anesthetic.

Levobupivacaine HCl

B1784-50 50 mg
EUR 128
Description: Levobupivacaine HCl, the pure S(-)-enantiomer of bupivacaine, is a long-acting local anesthetic.

Mechlorethamine HCl

B1785-5.1 10 mM (in 1mL DMSO)
EUR 119
Description: Mechlorethamine is the prototype of alkylating agents, it works by binding to DNA, crosslinking two strands and preventing cell duplication.

Mechlorethamine HCl

B1785-50 50 mg
EUR 128
Description: Mechlorethamine is the prototype of alkylating agents, it works by binding to DNA, crosslinking two strands and preventing cell duplication.

Mexiletine HCl

B1789-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: Mexiletine HCl belongs to Class IB anti-arrhythmic group of medicines, inhibits sodium channels to reduce the inward sodium current.

Mexiletine HCl

B1789-50 50 mg
EUR 128
Description: Mexiletine HCl belongs to Class IB anti-arrhythmic group of medicines, inhibits sodium channels to reduce the inward sodium current.

Minocycline HCl

B1791-100 100 mg
EUR 119
Description: Minocycline is a tetracycline antibiotic with neuroprotective, antiapoptotic, anti-inflammatory and antimicrobial effects.

Minocycline HCl

B1791-50 50 mg
EUR 108
Description: Minocycline is a tetracycline antibiotic with neuroprotective, antiapoptotic, anti-inflammatory and antimicrobial effects.

Nefopam HCl

B1794-10 10 mg
EUR 119
Description: Nefopam HCl is an centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.

Nefopam HCl

B1794-5.1 10 mM (in 1mL H2O)
EUR 132
Description: Nefopam HCl is an centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.

Nefopam HCl

B1794-50 50 mg
EUR 174
Description: Nefopam HCl is an centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.