Zardaverine |
A dual inhibitor of PDE3 and PDE4 (IC50s = 0.617 and 1.738 µM, respe… |
5 mg |
29685-5 |
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Z-Asp-CH2-DCB |
A pan-caspase inhibitor that blocks apoptosis, prevents the production of… |
10 mg |
15143-10 |
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Z-Asp-CH2-DCB |
A pan-caspase inhibitor that blocks apoptosis, prevents the production of… |
25 mg |
15143-25 |
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Z-Asp-CH2-DCB |
A pan-caspase inhibitor that blocks apoptosis, prevents the production of… |
5 mg |
15143-5 |
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Z-Asp-CH2-DCB |
A pan-caspase inhibitor that blocks apoptosis, prevents the production of… |
50 mg |
15143-50 |
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Zatebradine (hydrochloride) |
Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… |
10 mg |
18608-10 |
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Zatebradine (hydrochloride) |
Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… |
25 mg |
18608-25 |
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Zatebradine (hydrochloride) |
Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… |
5 mg |
18608-5 |
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Zatebradine (hydrochloride) |
Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… |
50 mg |
18608-50 |
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(Z)-Capsaicin |
An alkaloid with diverse biological activities; an agonist of TRPV1 (EC50… |
10 mg |
39929-10 |
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(Z)-Capsaicin |
An alkaloid with diverse biological activities; an agonist of TRPV1 (EC50… |
100 mg |
39929-100 |
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(Z)-Capsaicin |
An alkaloid with diverse biological activities; an agonist of TRPV1 (EC50… |
5 mg |
39929-5 |
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(Z)-Capsaicin |
An alkaloid with diverse biological activities; an agonist of TRPV1 (EC50… |
50 mg |
39929-50 |
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Z-CITCO |
An agonist of CAR (EC50 = 3.9 µM for the human receptor in a reporte… |
1 mg |
39172-1 |
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Z-CITCO |
An agonist of CAR (EC50 = 3.9 µM for the human receptor in a reporte… |
10 mg |
39172-10 |
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Z-CITCO |
An agonist of CAR (EC50 = 3.9 µM for the human receptor in a reporte… |
25 mg |
39172-25 |
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Z-CITCO |
An agonist of CAR (EC50 = 3.9 µM for the human receptor in a reporte… |
5 mg |
39172-5 |
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ZCL 278 |
A cell-permeable inhibitor of Cdc42, blocking interaction with the GEF int… |
10 mg |
14849-10 |
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ZCL 278 |
A cell-permeable inhibitor of Cdc42, blocking interaction with the GEF int… |
25 mg |
14849-25 |
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ZCL 278 |
A cell-permeable inhibitor of Cdc42, blocking interaction with the GEF int… |
5 mg |
14849-5 |
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ZCL 278 |
A cell-permeable inhibitor of Cdc42, blocking interaction with the GEF int… |
50 mg |
14849-50 |
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ZD 7288 |
A potent blocker of HCN channels that inhibits HCN4 more potently than HCN… |
10 mg |
15228-10 |
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ZD 7288 |
A potent blocker of HCN channels that inhibits HCN4 more potently than HCN… |
25 mg |
15228-25 |
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ZD 7288 |
A potent blocker of HCN channels that inhibits HCN4 more potently than HCN… |
5 mg |
15228-5 |
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ZD 7288 |
A potent blocker of HCN channels that inhibits HCN4 more potently than HCN… |
50 mg |
15228-50 |
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Z-D-Arg-Gly-Arg-pNA (hydrochloride) |
A colorimetric Factor Xa substrate; cleavage of the RGR peptide sequence r… |
1 mg |
27583-1 |
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Z-D-Arg-Gly-Arg-pNA (hydrochloride) |
A colorimetric Factor Xa substrate; cleavage of the RGR peptide sequence r… |
10 mg |
27583-10 |
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Z-D-Arg-Gly-Arg-pNA (hydrochloride) |
A colorimetric Factor Xa substrate; cleavage of the RGR peptide sequence r… |
25 mg |
27583-25 |
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Z-D-Arg-Gly-Arg-pNA (hydrochloride) |
A colorimetric Factor Xa substrate; cleavage of the RGR peptide sequence r… |
5 mg |
27583-5 |
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Z-DEVD-AFC |
A fluorogenic substrate for caspase-3; AFC is released upon cleavage by ca… |
1 mg |
24564-1 |
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Z-DEVD-CMK (trifluoroacetate salt) |
An irreversible protease inhibitor; irreversibly inhibits recombinant casp… |
1 mg |
27149-1 |
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Z-DEVD-CMK (trifluoroacetate salt) |
An irreversible protease inhibitor; irreversibly inhibits recombinant casp… |
5 mg |
27149-5 |
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Z-DEVD-CMK (trifluoroacetate salt) |
An irreversible protease inhibitor; irreversibly inhibits recombinant casp… |
500 µg |
27149-500 |
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Z-DEVD-FMK |
A cell-permeable irreversible inhibitor of caspase-3 (IC50 = 130 nM); pote… |
1 mg |
14414-1 |
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Z-DEVD-FMK |
A cell-permeable irreversible inhibitor of caspase-3 (IC50 = 130 nM); pote… |
5 mg |
14414-5 |
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Z-DEVD-FMK |
A cell-permeable irreversible inhibitor of caspase-3 (IC50 = 130 nM); pote… |
500 µg |
14414-500 |
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(Z-DEVD)2-Rh 110 (trifluoroacetate salt) |
A fluorogenic substrate for caspase-3; rhodamine 110 is released upon enzy… |
1 mg |
27432-1 |
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(Z-DEVD)2-Rh 110 (trifluoroacetate salt) |
A fluorogenic substrate for caspase-3; rhodamine 110 is released upon enzy… |
500 µg |
27432-500 |
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ZD 7155 (hydrochloride) |
An AT1 receptor antagonist (IC50 = 3.3 nM); inhibits angiotensin II-induce… |
1 mg |
36576-1 |
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ZD 7155 (hydrochloride) |
An AT1 receptor antagonist (IC50 = 3.3 nM); inhibits angiotensin II-induce… |
10 mg |
36576-10 |
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ZD 7155 (hydrochloride) |
An AT1 receptor antagonist (IC50 = 3.3 nM); inhibits angiotensin II-induce… |
25 mg |
36576-25 |
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ZD 7155 (hydrochloride) |
An AT1 receptor antagonist (IC50 = 3.3 nM); inhibits angiotensin II-induce… |
5 mg |
36576-5 |
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11(Z)-Docosenoic Acid |
A 22-carbon monounsaturated fatty acid; has been found in fish oil |
1 mg |
34582-1 |
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13(Z)-Docosenoic Acid |
13(Z)-Docosenoic acid is a 22-carbon monounsaturated fatty acid. It is fou… |
100 mg |
90175-100 |
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13(Z)-Docosenoic Acid |
13(Z)-Docosenoic acid is a 22-carbon monounsaturated fatty acid. It is fou… |
250 mg |
90175-250 |
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13(Z)-Docosenoic Acid |
13(Z)-Docosenoic acid is a 22-carbon monounsaturated fatty acid. It is fou… |
50 mg |
90175-50 |
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13(Z)-Docosenoic Acid |
13(Z)-Docosenoic acid is a 22-carbon monounsaturated fatty acid. It is fou… |
500 mg |
90175-500 |
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13(Z)-Docosenoic Acid methyl ester |
A fatty acid methyl ester; a flavor-active, volatile, and aromatic compoun… |
100 mg |
20568-100 |
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13(Z)-Docosenoic Acid methyl ester |
A fatty acid methyl ester; a flavor-active, volatile, and aromatic compoun… |
250 mg |
20568-250 |
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13(Z)-Docosenoic Acid methyl ester |
A fatty acid methyl ester; a flavor-active, volatile, and aromatic compoun… |
50 mg |
20568-50 |
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