13925 Results for: "Ranitidine+hydrochloride"

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 slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 10 mg

Supplier: Cayman Chemical

A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 10 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 * 100 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 * 100 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 * 10 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 * 10 mg

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LY2584702 Hydrochloride_5mg pack 1 * 5 mg

Supplier: Apollo Scientific

LY2584702 Hydrochloride_5mg pack 1 * 5 mg

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1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 1 mg

Supplier: Cayman Chemical

1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 1 mg

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An active metabolite of proguanil, produced by CYP2C19 1 * 50 mg

Supplier: Cayman Chemical

An active metabolite of proguanil, produced by CYP2C19 1 * 50 mg

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A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 5 mg

Supplier: Cayman Chemical

A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 5 mg

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A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 5 mg

Supplier: Cayman Chemical

A selective antagonist of GABAB receptors (IC50 = 43 µM) 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 * 1 g

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 * 1 g

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A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 10 mg

Supplier: Cayman Chemical

A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 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 * 50 mg

Supplier: Cayman Chemical

A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 50 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 slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 5 mg

Supplier: Cayman Chemical

A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 5 mg

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A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 10 mg

Supplier: Cayman Chemical

A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 10 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 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