32304 Results for: "tert-Butylhydrazine+hydrochloride"
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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An epimer of chlortetracycline 1 * 1 mg
Supplier: Cayman Chemical
An epimer of chlortetracycline 1 * 1 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 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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1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 10 mg
Supplier: Cayman Chemical
1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 10 mg
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A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 1 mg
Supplier: Cayman Chemical
A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 1 mg
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An inhibitor of JAK3 (IC50 = 79 nM) 1 * 1 mg
Supplier: Cayman Chemical
An inhibitor of JAK3 (IC50 = 79 nM) 1 * 1 mg
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A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 1 mg
Supplier: Cayman Chemical
A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 1 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 * 50 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 * 50 mg
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A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 5 mg
Supplier: Cayman Chemical
A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 5 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 * 1 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 * 1 mg
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An active metabolite of proguanil, produced by CYP2C19 1 * 10 mg
Supplier: Cayman Chemical
An active metabolite of proguanil, produced by CYP2C19 1 * 10 mg
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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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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 5 mg
Supplier: Cayman Chemical
A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 5 mg
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A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 100 mg
Supplier: Cayman Chemical
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 100 mg
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A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 1 mg
Supplier: Cayman Chemical
A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 1 mg
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A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 100 mg
Supplier: Cayman Chemical
A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 100 mg
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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 100 mg
Supplier: Cayman Chemical
1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 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 * 1 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 * 1 g
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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 * 5 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 * 5 g
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A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric channels (IC50 = 0.75 and 0.71 µM, respectively) as well as KCNQ2+3 heteromultimers (IC50 = 0.6 µM) 1 * 5 mg
Supplier: Cayman Chemical
A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric channels (IC50 = 0.75 and 0.71 µM, respectively) as well as KCNQ2+3 heteromultimers (IC50 = 0.6 µM) 1 * 5 mg
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An inhibitor of PARPs which can be used in cells or in animals 1 * 10 mg
Supplier: Cayman Chemical
An inhibitor of PARPs which can be used in cells or in animals 1 * 10 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
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A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 5 mg
Supplier: Cayman Chemical
A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 5 mg
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A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 5 mg
Supplier: Cayman Chemical
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 5 mg
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A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 10 mg
Supplier: Cayman Chemical
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 10 mg
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A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 50 mg
Supplier: Cayman Chemical
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 50 mg
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A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 10 mg
Supplier: Cayman Chemical
A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 10 mg
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An orally active, selective inhibitor of Cdk4 (IC50 = 11 nM) and Cdk6 (IC50 = 16 nM) with antiproliferative activity against retinob lastoma-positive tumor cells, blocking retinoblastoma phosphorylation and inducing G1 arrest 1 * 25 mg
Supplier: Cayman Chemical
An orally active, selective inhibitor of Cdk4 (IC50 = 11 nM) and Cdk6 (IC50 = 16 nM) with antiproliferative activity against retinob lastoma-positive tumor cells, blocking retinoblastoma phosphorylation and inducing G1 arrest 1 * 25 mg