18149 Results for: "Fluoxetine+hydrochloride"

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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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 pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 10 mg

Supplier: Cayman Chemical

A pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 10 mg

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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 10 mg

Supplier: Cayman Chemical

A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 10 mg

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A major active metabolite of saxagliptin inhibits DPP-4 (Ki = 2.6 nM for human recombinant enzyme) 1 * 1 mg

Supplier: Cayman Chemical

A major active metabolite of saxagliptin inhibits DPP-4 (Ki = 2.6 nM for human recombinant enzyme) 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 * 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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A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 1 mg

Supplier: Cayman Chemical

A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 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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GDC_0994 hydrochloride_25mg pack 1 * 25 mg

Supplier: Apollo Scientific

GDC_0994 hydrochloride_25mg pack 1 * 25 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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BMS_582949 hydrochloride_5mg pack 1 * 5 mg

Supplier: Apollo Scientific

BMS_582949 hydrochloride_5mg pack 1 * 5 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 slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 500 µG

Supplier: Cayman Chemical

A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 500 µG

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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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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 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