Zingibroside R1 |
A triterpene saponin and an active metabolite of ginsenoside Ro; cytotoxic… |
5 mg |
34130-5 |
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Zinnol |
A fungal metabolite |
1 mg |
29168-1 |
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Zinpyr-1 |
A cell-permeable, fluorescein-based probe for zinc detection; undergoes a… |
1 mg |
15122-1 |
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Zinpyr-1 |
A cell-permeable, fluorescein-based probe for zinc detection; undergoes a… |
10 mg |
15122-10 |
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Zinpyr-1 |
A cell-permeable, fluorescein-based probe for zinc detection; undergoes a… |
5 mg |
15122-5 |
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Zinquin ethyl ester |
A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… |
1 mg |
15133-1 |
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Zinquin ethyl ester |
A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… |
10 mg |
15133-10 |
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Zinquin ethyl ester |
A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… |
5 mg |
15133-5 |
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Zinquin ethyl ester |
A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… |
500 µg |
15133-500 |
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Ziprasidone-d8 |
An internal standard for the quantification of ziprasidone by GC- or LC-MS |
1 mg |
30737-1 |
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Ziprasidone (hydrochloride hydrate) |
An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… |
10 mg |
15031-10 |
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Ziprasidone (hydrochloride hydrate) |
An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… |
25 mg |
15031-25 |
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Ziprasidone (hydrochloride hydrate) |
An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… |
5 mg |
15031-5 |
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Ziprasidone (hydrochloride hydrate) |
An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… |
50 mg |
15031-50 |
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Ziptide (trifluoroacetate salt) |
A peptide substrate for various serine / threonine protein kinases; has be… |
1 mg |
37466-1 |
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Ziptide (trifluoroacetate salt) |
A peptide substrate for various serine / threonine protein kinases; has be… |
10 mg |
37466-10 |
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Ziptide (trifluoroacetate salt) |
A peptide substrate for various serine / threonine protein kinases; has be… |
25 mg |
37466-25 |
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Ziptide (trifluoroacetate salt) |
A peptide substrate for various serine / threonine protein kinases; has be… |
5 mg |
37466-5 |
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Ziyuglycoside I |
A triterpenoid saponin with diverse biological activities; increases the s… |
1 mg |
37320-1 |
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Ziyuglycoside I |
A triterpenoid saponin with diverse biological activities; increases the s… |
10 mg |
37320-10 |
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Ziyuglycoside I |
A triterpenoid saponin with diverse biological activities; increases the s… |
25 mg |
37320-25 |
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Ziyuglycoside I |
A triterpenoid saponin with diverse biological activities; increases the s… |
5 mg |
37320-5 |
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Ziyuglycoside II |
A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… |
10 mg |
40831-10 |
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Ziyuglycoside II |
A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… |
25 mg |
40831-25 |
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Ziyuglycoside II |
A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… |
5 mg |
40831-5 |
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Ziyuglycoside II |
A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… |
50 mg |
40831-50 |
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ZK 159222 |
An antagonist of the vitamin D receptor; inhibits VDR-mediated target gene… |
500 µg |
9001925-500 |
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ZK 824859 |
An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… |
10 mg |
37789-10 |
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ZK 824859 |
An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… |
25 mg |
37789-25 |
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ZK 824859 |
An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… |
5 mg |
37789-5 |
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ZK 824859 |
An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… |
50 mg |
37789-50 |
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ZK 756326 (hydrochloride) |
A non-peptide agonist of CCR8; inhibits binding of CCL1 to human CCR8 (IC5… |
10 mg |
28454-10 |
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ZK 756326 (hydrochloride) |
A non-peptide agonist of CCR8; inhibits binding of CCL1 to human CCR8 (IC5… |
25 mg |
28454-25 |
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ZK 756326 (hydrochloride) |
A non-peptide agonist of CCR8; inhibits binding of CCL1 to human CCR8 (IC5… |
5 mg |
28454-5 |
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ZK118182 isopropyl ester |
A prodrug formulation of a potent DP-receptor agonist that is designed to… |
100 µg |
13673-100 |
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ZK118182 isopropyl ester |
A prodrug formulation of a potent DP-receptor agonist that is designed to… |
500 µg |
13673-500 |
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ZL006 |
An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… |
10 mg |
34147-10 |
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ZL006 |
An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… |
25 mg |
34147-25 |
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ZL006 |
An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… |
5 mg |
34147-5 |
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ZL006 |
An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… |
50 mg |
34147-50 |
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ZL0420 |
A BRD4 inhibitor; inhibits BD1 and BD2 in BRD4 (IC50s = 27 and 32 nM, resp… |
10 mg |
30741-10 |
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ZL0420 |
A BRD4 inhibitor; inhibits BD1 and BD2 in BRD4 (IC50s = 27 and 32 nM, resp… |
25 mg |
30741-25 |
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ZL0420 |
A BRD4 inhibitor; inhibits BD1 and BD2 in BRD4 (IC50s = 27 and 32 nM, resp… |
5 mg |
30741-5 |
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Z-(L-Arg)-AMC (hydrochloride) |
A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… |
10 mg |
30797-10 |
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Z-(L-Arg)-AMC (hydrochloride) |
A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… |
100 mg |
30797-100 |
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Z-(L-Arg)-AMC (hydrochloride) |
A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… |
25 mg |
30797-25 |
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Z-(L-Arg)-AMC (hydrochloride) |
A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… |
50 mg |
30797-50 |
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ZLD1039 |
An inhibitor of EZH2 (IC50 = 5.6 nM); selective for EZH2 over EZH1 (IC50 =… |
1 mg |
19218-1 |
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ZLD1039 |
An inhibitor of EZH2 (IC50 = 5.6 nM); selective for EZH2 over EZH1 (IC50 =… |
5 mg |
19218-5 |
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Z-Leu-Leu-Leu-B(OH)2 |
A proteasome inhibitor with diverse biological activities; inhibits LPS-in… |
1 mg |
10008311-1 |
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