1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl) 99 % Coupling reagent for peptide synthesis Empirical formula C8H17N3 . HCl Molar mass (M) 191,7 g/mol Melting point (mp)110-115 °C Solubility soluble (H2O, 20 °C) Storage temp.: - 1 * 5 g
Supplier: Roth Carl
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl) 99 % Coupling reagent for peptide synthesis Empirical formula C8H17N3 . HCl Molar mass (M) 191,7 g/mol Melting point (mp)110-115 °C Solubility soluble (H2O, 20 °C) Storage temp.: - 1 * 5 g
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2-pyrimidinemethanamine, monohydrochloride 1 * 1 g
Supplier: Cayman Chemical
2-pyrimidinemethanamine, monohydrochloride 1 * 1 g
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A tricyclic antidepressant that potently inhibits serotonin and norepinephrine reuptake (Kis = 7.4 and 96 nM, respectively) 1 * 1 g
Supplier: Cayman Chemical
A tricyclic antidepressant that potently inhibits serotonin and norepinephrine reuptake (Kis = 7.4 and 96 nM, respectively) 1 * 1 g
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An epimer of chlortetracycline 1 * 5 mg
Supplier: Cayman Chemical
An epimer of chlortetracycline 1 * 5 mg
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An epimer of chlortetracycline 1 * 500 µG
Supplier: Cayman Chemical
An epimer of chlortetracycline 1 * 500 µG
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A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 5 g
Supplier: Cayman Chemical
A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 5 g
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An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg
Supplier: Cayman Chemical
An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg
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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g
Supplier: Cayman Chemical
A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g
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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g
Supplier: Cayman Chemical
A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g
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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg
Supplier: Cayman Chemical
A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg
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A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg
Supplier: Cayman Chemical
A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg
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A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 25 mg
Supplier: Cayman Chemical
A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 25 mg
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A potent, cell-permeable inhibitor of SET7/9 (IC50 = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases 1 * 5 mg
Supplier: Cayman Chemical
A potent, cell-permeable inhibitor of SET7/9 (IC50 = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases 1 * 5 mg
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GDC_0994 hydrochloride_5mg pack 1 * 5 mg
Supplier: Apollo Scientific
GDC_0994 hydrochloride_5mg pack 1 * 5 mg
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A prodrug of benazeprilat inhibits enzymatic activity of partially purified ACE isolated from rabbit lung (IC50 = 2 nM) 1 * 50 mg
Supplier: Cayman Chemical
A prodrug of benazeprilat inhibits enzymatic activity of partially purified ACE isolated from rabbit lung (IC50 = 2 nM) 1 * 50 mg
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A β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that relaxes human arteries and veins with ED50 val ues of 40-50 µM in vitro 1 * 1 mg
Supplier: Cayman Chemical
A β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that relaxes human arteries and veins with ED50 val ues of 40-50 µM in vitro 1 * 1 mg
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A β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that relaxes human arteries and veins with ED50 val ues of 40-50 µM in vitro 1 * 5 mg
Supplier: Cayman Chemical
A β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that relaxes human arteries and veins with ED50 val ues of 40-50 µM in vitro 1 * 5 mg
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A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 1 mg
Supplier: Cayman Chemical
A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 1 mg
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LY2584702 Hydrochloride_50mg pack 1 * 50 mg
Supplier: Apollo Scientific
LY2584702 Hydrochloride_50mg pack 1 * 50 mg
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SB_203580 Hydrochloride_50mg pack 1 * 50 mg
Supplier: Apollo Scientific
SB_203580 Hydrochloride_50mg pack 1 * 50 mg
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A first generation tricyclic antidepressant 1 * 5 g
Supplier: Cayman Chemical
A first generation tricyclic antidepressant 1 * 5 g
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An active metabolite of proguanil, produced by CYP2C19 1 * 25 mg
Supplier: Cayman Chemical
An active metabolite of proguanil, produced by CYP2C19 1 * 25 mg
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An inhibitor of JAK3 (IC50 = 79 nM) 1 * 5 mg
Supplier: Cayman Chemical
An inhibitor of JAK3 (IC50 = 79 nM) 1 * 5 mg
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A fluoroquinolone antibiotic that displays broad spectrum antibacterial activity by inhibiting the bacterial regulatory enzyme DNA g yrase (IC50 = 0.92 µg/ml) as well as topoisomerase IV (IC50 = 1.62 µg/ml) 1 * 100 mg
Supplier: Cayman Chemical
A fluoroquinolone antibiotic that displays broad spectrum antibacterial activity by inhibiting the bacterial regulatory enzyme DNA g yrase (IC50 = 0.92 µg/ml) as well as topoisomerase IV (IC50 = 1.62 µg/ml) 1 * 100 mg
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A conventional antipsychotic drug that potently activates several neuroreceptors, including serotonin (Kis = 10, 60, and 57 nM for 5 -HT2A, 5-HT2C, and 5-HT6, respectively), dopamine D2 (Ki = 11 nM), and adrenergic 1A (Ki = 5 nM) receptors 1 * 25 g
Supplier: Cayman Chemical
A conventional antipsychotic drug that potently activates several neuroreceptors, including serotonin (Kis = 10, 60, and 57 nM for 5 -HT2A, 5-HT2C, and 5-HT6, respectively), dopamine D2 (Ki = 11 nM), and adrenergic 1A (Ki = 5 nM) receptors 1 * 25 g
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A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 1 mg
Supplier: Cayman Chemical
A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 1 mg
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A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 10 mg
Supplier: Cayman Chemical
A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 10 mg
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1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 5 mg
Supplier: Cayman Chemical
1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 5 mg
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A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 100 mg
Supplier: Cayman Chemical
A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 100 mg