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18023 results for "Fluoxetine+hydrochloride"

18023 Results for: "Fluoxetine+hydrochloride"

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

Supplier: Cayman Chemical

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

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1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 5 mg

Supplier: Cayman Chemical

1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 5 mg

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An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg

Supplier: Cayman Chemical

An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg

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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g

Supplier: Cayman Chemical

A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g

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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g

Supplier: Cayman Chemical

A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g

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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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A gastroprotective histamine H2 receptor antagonist (pKi = 7.1) that decreases gastric acid secretion and inhibits intracellular cAM P production (IC50 = 1 µM) 1 * 1 g

Supplier: Cayman Chemical

A gastroprotective histamine H2 receptor antagonist (pKi = 7.1) that decreases gastric acid secretion and inhibits intracellular cAM P production (IC50 = 1 µM) 1 * 1 g

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A gastroprotective histamine H2 receptor antagonist (pKi = 7.1) that decreases gastric acid secretion and inhibits intracellular cAM P production (IC50 = 1 µM) 1 * 5 g

Supplier: Cayman Chemical

A gastroprotective histamine H2 receptor antagonist (pKi = 7.1) that decreases gastric acid secretion and inhibits intracellular cAM P production (IC50 = 1 µM) 1 * 5 g

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2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 50 mg

Supplier: Cayman Chemical

2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 50 mg

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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg

Supplier: Cayman Chemical

A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg

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A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg

Supplier: Cayman Chemical

A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 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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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 first generation tricyclic antidepressant 1 * 5 g

Supplier: Cayman Chemical

A first generation tricyclic antidepressant 1 * 5 g

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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 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 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 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 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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GDC_0994 hydrochloride_5mg pack 1 * 5 mg

Supplier: Apollo Scientific

GDC_0994 hydrochloride_5mg pack 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 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 prodrug of benazeprilat inhibits enzymatic activity of partially purified ACE isolated from rabbit lung (IC50 = 2 nM) 1 * 50 mg

Supplier: Cayman Chemical

A prodrug of benazeprilat inhibits enzymatic activity of partially purified ACE isolated from rabbit lung (IC50 = 2 nM) 1 * 50 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

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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 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 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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