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 |
More Info
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Ziprasidone (hydrochloride hydrate) |
An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… |
5 mg |
15031-5 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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Z-Leu-Leu-Leu-B(OH)2 |
A proteasome inhibitor with diverse biological activities; inhibits LPS-in… |
200 µg |
10008311-200 |
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(Z)-Ligustilide |
A phthalide with diverse biological activities; inhibits autophagy and res… |
100 mg |
26908-100 |
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(Z)-Ligustilide |
A phthalide with diverse biological activities; inhibits autophagy and res… |
25 mg |
26908-25 |
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(Z)-Ligustilide |
A phthalide with diverse biological activities; inhibits autophagy and res… |
50 mg |
26908-50 |
More Info
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ZLJ-6 |
A dual inhibitor of COX and 5-LO enzymes (IC50 = 0.73, 0.31, and 0.99 &mic… |
1 mg |
13271-1 |
More Info
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ZLJ-6 |
A dual inhibitor of COX and 5-LO enzymes (IC50 = 0.73, 0.31, and 0.99 &mic… |
10 mg |
13271-10 |
More Info
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ZLJ-6 |
A dual inhibitor of COX and 5-LO enzymes (IC50 = 0.73, 0.31, and 0.99 &mic… |
25 mg |
13271-25 |
More Info
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ZLJ-6 |
A dual inhibitor of COX and 5-LO enzymes (IC50 = 0.73, 0.31, and 0.99 &mic… |
5 mg |
13271-5 |
More Info
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Z-LLE-AMC |
A fluorogenic substrate for the caspase-like post-glutamate peptide hydrol… |
1 mg |
10008117-1 |
More Info
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Z-LLE-AMC |
A fluorogenic substrate for the caspase-like post-glutamate peptide hydrol… |
10 mg |
10008117-10 |
More Info
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Z-LLE-AMC |
A fluorogenic substrate for the caspase-like post-glutamate peptide hydrol… |
5 mg |
10008117-5 |
More Info
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Z-LLL-AMC |
A fluorogenic substrate for the chymotrypsin-like activity of the 26S prot… |
1 mg |
10008118-1 |
More Info
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Z-LLL-AMC |
A fluorogenic substrate for the chymotrypsin-like activity of the 26S prot… |
10 mg |
10008118-10 |
More Info
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Z-LLL-AMC |
A fluorogenic substrate for the chymotrypsin-like activity of the 26S prot… |
5 mg |
10008118-5 |
More Info
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ZLN005 |
A small molecule that stimulates the expression of PGC-1α and downst… |
10 mg |
14121-10 |
More Info
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ZLN005 |
A small molecule that stimulates the expression of PGC-1α and downst… |
25 mg |
14121-25 |
More Info
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ZLN005 |
A small molecule that stimulates the expression of PGC-1α and downst… |
5 mg |
14121-5 |
More Info
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ZLN005 |
A small molecule that stimulates the expression of PGC-1α and downst… |
50 mg |
14121-50 |
More Info
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ZLN024 |
An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… |
10 mg |
21644-10 |
More Info
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ZLN024 |
An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… |
25 mg |
21644-25 |
More Info
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ZLN024 |
An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… |
5 mg |
21644-5 |
More Info
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ZLN024 |
An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… |
50 mg |
21644-50 |
More Info
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ZLN005 (hydrochloride) |
A small molecule that stimulates the expression of PGC-1α and downst… |
10 mg |
9002449-10 |
More Info
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ZLN005 (hydrochloride) |
A small molecule that stimulates the expression of PGC-1α and downst… |
25 mg |
9002449-25 |
More Info
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ZLN005 (hydrochloride) |
A small molecule that stimulates the expression of PGC-1α and downst… |
5 mg |
9002449-5 |
More Info
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ZLN005 (hydrochloride) |
A small molecule that stimulates the expression of PGC-1α and downst… |
50 mg |
9002449-50 |
More Info
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Z-L-Phe-CMK |
An inhibitor of SARS-CoV Mpro (Ki = 306 nM); selective for SARS-CoV Mpro o… |
1 g |
15225-1 |
More Info
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Z-L-Phe-CMK |
An inhibitor of SARS-CoV Mpro (Ki = 306 nM); selective for SARS-CoV Mpro o… |
250 mg |
15225-250 |
More Info
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Z-L-Phe-CMK |
An inhibitor of SARS-CoV Mpro (Ki = 306 nM); selective for SARS-CoV Mpro o… |
500 mg |
15225-500 |
More Info
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Z-LRGG-AMC (trifluoroacetate salt) |
A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… |
10 mg |
26641-10 |
More Info
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Z-LRGG-AMC (trifluoroacetate salt) |
A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… |
25 mg |
26641-25 |
More Info
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Z-LRGG-AMC (trifluoroacetate salt) |
A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… |
5 mg |
26641-5 |
More Info
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Z-LRGG-AMC (trifluoroacetate salt) |
A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… |
50 mg |
26641-50 |
More Info
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ZLY032 |
A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… |
10 mg |
31485-10 |
More Info
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ZLY032 |
A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… |
25 mg |
31485-25 |
More Info
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ZLY032 |
A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… |
5 mg |
31485-5 |
More Info
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ZLY032 |
A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… |
50 mg |
31485-50 |
More Info
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ZLY28 |
An FXR agonist and inhibitor of FABP1; selectively induces reporter gene e… |
1 mg |
38864-1 |
More Info
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ZLY28 |
An FXR agonist and inhibitor of FABP1; selectively induces reporter gene e… |
5 mg |
38864-5 |
More Info
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Z-Lys-OBzl (benzenesulfonate) |
An amino acid-containing building block |
1 g |
30916-1 |
More Info
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Z-Lys-OBzl (benzenesulfonate) |
An amino acid-containing building block |
500 mg |
30916-500 |
More Info
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Z-Lys-OH |
An amino acid building block; has been used in the synthesis of peptidomim… |
1 g |
30460-1 |
More Info
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Z-Lys-OH |
An amino acid building block; has been used in the synthesis of peptidomim… |
10 g |
30460-10 |
More Info
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Z-Lys-OH |
An amino acid building block; has been used in the synthesis of peptidomim… |
5 g |
30460-5 |
More Info
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Z-Lys-OMe (hydrochloride) |
A synthetic intermediate; has been used in the synthesis of peptide enzyme… |
1 g |
30804-1 |
More Info
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Z-Lys-OMe (hydrochloride) |
A synthetic intermediate; has been used in the synthesis of peptide enzyme… |
100 mg |
30804-100 |
More Info
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Z-Lys-OMe (hydrochloride) |
A synthetic intermediate; has been used in the synthesis of peptide enzyme… |
250 mg |
30804-250 |
More Info
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Z-Lys-OMe (hydrochloride) |
A synthetic intermediate; has been used in the synthesis of peptide enzyme… |
500 mg |
30804-500 |
More Info
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ZM 241385 |
A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… |
1 mg |
20447-1 |
More Info
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ZM 241385 |
A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… |
10 mg |
20447-10 |
More Info
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