21863 Results for: "Benzyl+thioacetimidate+hydrochloride"

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A tricyclic antidepressant that potently inhibits serotonin and norepinephrine reuptake (Kis = 7.4 and 96 nM, respectively) 1 * 1 g

Supplier: Cayman Chemical

A tricyclic antidepressant that potently inhibits serotonin and norepinephrine reuptake (Kis = 7.4 and 96 nM, respectively) 1 * 1 g

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An epimer of chlortetracycline 1 * 5 mg

Supplier: Cayman Chemical

An epimer of chlortetracycline 1 * 5 mg

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An epimer of chlortetracycline 1 * 500 µG

Supplier: Cayman Chemical

An epimer of chlortetracycline 1 * 500 µG

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A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 5 g

Supplier: Cayman Chemical

A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 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 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 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

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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 cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 5 mg

Supplier: Cayman Chemical

A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 5 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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A pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 1 mg

Supplier: Cayman Chemical

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

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A pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 5 mg

Supplier: Cayman Chemical

A pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 5 mg

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A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 1 g

Supplier: Cayman Chemical

A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 1 g

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

Supplier: Cayman Chemical

An inhibitor of JAK3 (IC50 = 79 nM) 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 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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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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GDC_0994 hydrochloride_5mg pack 1 * 5 mg

Supplier: Apollo Scientific

GDC_0994 hydrochloride_5mg pack 1 * 5 mg

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2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 10 mg

Supplier: Cayman Chemical

2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 10 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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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 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