(±)-Propranolol (hydrochloride) |
A β-adrenergic receptor antagonist (Kds = 6.91, 0.832, and 117.49 nM… |
25 g |
23349-25 |
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(±)-Propranolol (hydrochloride) |
A β-adrenergic receptor antagonist (Kds = 6.91, 0.832, and 117.49 nM… |
5 g |
23349-5 |
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(±)-Propranolol (hydrochloride) |
A β-adrenergic receptor antagonist (Kds = 6.91, 0.832, and 117.49 nM… |
50 g |
23349-50 |
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(±)-2-propyl-4-Pentenoic Acid |
A metabolite of valproic acid; undergoes β-oxidation to form reactive… |
10 mg |
23090-10 |
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(±)-2-propyl-4-Pentenoic Acid |
A metabolite of valproic acid; undergoes β-oxidation to form reactive… |
100 mg |
23090-100 |
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(±)-2-propyl-4-Pentenoic Acid |
A metabolite of valproic acid; undergoes β-oxidation to form reactive… |
25 mg |
23090-25 |
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(±)-2-propyl-4-Pentenoic Acid |
A metabolite of valproic acid; undergoes β-oxidation to form reactive… |
50 mg |
23090-50 |
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(±)-Rolipram |
A cell-permeable selective PDE4 inhibitor |
10 mg |
10011132-10 |
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(±)-Rolipram |
A cell-permeable selective PDE4 inhibitor |
25 mg |
10011132-25 |
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(±)-Rolipram |
A cell-permeable selective PDE4 inhibitor |
5 mg |
10011132-5 |
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(±)-Salsolidine |
An alkaloid; inhibits COMT (Ki = 190 µM) |
100 mg |
32953-100 |
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(±)-Salsolidine |
An alkaloid; inhibits COMT (Ki = 190 µM) |
25 mg |
32953-25 |
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(±)-Salsolidine |
An alkaloid; inhibits COMT (Ki = 190 µM) |
50 mg |
32953-50 |
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(±)-Salsolinol (hydrochloride) |
A metabolite of ethanol produced in the brain that stimulates dopamineric… |
100 mg |
15597-100 |
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(±)-Salsolinol (hydrochloride) |
A metabolite of ethanol produced in the brain that stimulates dopamineric… |
500 mg |
15597-500 |
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(±)-SDZ-201 106 |
A sodium channel opener that prolongs the open state of cardiac voltage-ga… |
10 mg |
21356-10 |
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(±)-SDZ-201 106 |
A sodium channel opener that prolongs the open state of cardiac voltage-ga… |
25 mg |
21356-25 |
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(±)-Sitagliptin-d4 (hydrochloride) |
An internal standard for the quantification sitagliptin by GC- or LC-MS, |
1 mg |
25042-1 |
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(±)-Sitagliptin-d4 (hydrochloride) |
An internal standard for the quantification sitagliptin by GC- or LC-MS, |
500 µg |
25042-500 |
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(±)-SKF 81297 (hydrobromide) |
A selective agonist of the dopamine D1-like receptor (Ki = 1.9 nM) that de… |
10 mg |
15067-10 |
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(±)-SKF 81297 (hydrobromide) |
A selective agonist of the dopamine D1-like receptor (Ki = 1.9 nM) that de… |
25 mg |
15067-25 |
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(±)-SKF 81297 (hydrobromide) |
A selective agonist of the dopamine D1-like receptor (Ki = 1.9 nM) that de… |
5 mg |
15067-5 |
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(±)-SLV 319 |
A mixture of the potent and selective CB1 receptor antagonist SLV 319 (Ki… |
1 mg |
10009226-1 |
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(±)-SLV 319 |
A mixture of the potent and selective CB1 receptor antagonist SLV 319 (Ki… |
10 mg |
10009226-10 |
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(±)-SLV 319 |
A mixture of the potent and selective CB1 receptor antagonist SLV 319 (Ki… |
5 mg |
10009226-5 |
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