17603 Results for: "3-Nitrobenzylamine+hydrochloride"

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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 * 250 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 * 250 mg

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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 50 mg

Supplier: Cayman Chemical

1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 50 mg

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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 10 mg

Supplier: Cayman Chemical

1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 10 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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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 * 500 mg

Supplier: Cayman Chemical

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An ATP-competitive, pan-Akt kinase inhibitor (IC50s = 2, 13, and 9 nM for Akt1, 2, and 3, respectively) that inhibits proliferation and induces apoptosis in various human tumor cells in vitro and in xenografts in immunocompromised mice 1 * 25 mg

Supplier: Cayman Chemical

An ATP-competitive, pan-Akt kinase inhibitor (IC50s = 2, 13, and 9 nM for Akt1, 2, and 3, respectively) that inhibits proliferation and induces apoptosis in various human tumor cells in vitro and in xenografts in immunocompromised mice 1 * 25 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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GDC_0994 hydrochloride_1mg pack 1 * 1 mg

Supplier: Apollo Scientific

GDC_0994 hydrochloride_1mg pack 1 * 1 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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A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 10 mg

Supplier: Cayman Chemical

A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 10 mg

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A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 5 mg

Supplier: Cayman Chemical

A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 5 mg

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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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GDC_0994 hydrochloride_25mg pack 1 * 25 mg

Supplier: Apollo Scientific

GDC_0994 hydrochloride_25mg pack 1 * 25 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 * 10 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 * 10 mg

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A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 10 mg

Supplier: Cayman Chemical

A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 10 mg

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A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 25 mg

Supplier: Cayman Chemical

A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 25 mg

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LY2584702 Hydrochloride_25mg pack 1 * 25 mg

Supplier: Apollo Scientific

LY2584702 Hydrochloride_25mg pack 1 * 25 mg

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An ATP-competitive, pan-Akt kinase inhibitor (IC50s = 2, 13, and 9 nM for Akt1, 2, and 3, respectively) that inhibits proliferation and induces apoptosis in various human tumor cells in vitro and in xenografts in immunocompromised mice 1 * 10 mg

Supplier: Cayman Chemical

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An antibiotic that can inhibit cell wall synthesis in plant-pathogenic oomycetes (MIC = 25 µg/ml for P. medicaginis M2913) and certa in fungi as well as some bacterial species (MIC = 400 µg/ml for S. aureus) 1 * 5 mg

Supplier: Cayman Chemical

An antibiotic that can inhibit cell wall synthesis in plant-pathogenic oomycetes (MIC = 25 µg/ml for P. medicaginis M2913) and certa in fungi as well as some bacterial species (MIC = 400 µg/ml for S. aureus) 1 * 5 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 * 5 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 * 5 mg