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18023 results for "Fluoxetine+hydrochloride"

18023 Results for: "Fluoxetine+hydrochloride"

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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SB_203580 Hydrochloride_100mg pack 1 * 100 mg

Supplier: Apollo Scientific

SB_203580 Hydrochloride_100mg pack 1 * 100 mg

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Ulixertinib hydrochloride_50mg pack 1 * 50 mg

Supplier: Apollo Scientific

Ulixertinib hydrochloride_50mg pack 1 * 50 mg

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BMS_582949 hydrochloride_25mg pack 1 * 25 mg

Supplier: Apollo Scientific

BMS_582949 hydrochloride_25mg pack 1 * 25 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 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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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 potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 5 mg

Supplier: Cayman Chemical

A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 5 mg

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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 * 1 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 * 1 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 * 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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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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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 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 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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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 -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 5 mg

Supplier: Cayman Chemical

A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 5 mg

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A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 5 mg

Supplier: Cayman Chemical

A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 5 mg

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Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 1 mg

Supplier: Cayman Chemical

Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 1 mg

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Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 5 mg

Supplier: Cayman Chemical

Selectively inhibits human NHE-1 with an IC50 value of 14 nM 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 * 5 mg

Supplier: Cayman Chemical

1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 5 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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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

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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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A first generation tricyclic antidepressant 1 * 5 g

Supplier: Cayman Chemical

A first generation tricyclic antidepressant 1 * 5 g

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