CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 649 of 652
Non-Antibody Products
Page 649 of 652
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Zingibroside R1 | A triterpene saponin and an active metabolite of ginsenoside Ro; cytotoxic… | 5 mg | 34130-5 | More Info |
| Zinnol | A fungal metabolite | 1 mg | 29168-1 | More Info |
| Zinpyr-1 | A cell-permeable, fluorescein-based probe for zinc detection; undergoes a… | 1 mg | 15122-1 | More Info |
| Zinpyr-1 | A cell-permeable, fluorescein-based probe for zinc detection; undergoes a… | 10 mg | 15122-10 | More Info |
| Zinpyr-1 | A cell-permeable, fluorescein-based probe for zinc detection; undergoes a… | 5 mg | 15122-5 | More Info |
| Zinquin ethyl ester | A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… | 1 mg | 15133-1 | More Info |
| Zinquin ethyl ester | A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… | 10 mg | 15133-10 | More Info |
| Zinquin ethyl ester | A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… | 5 mg | 15133-5 | More Info |
| Zinquin ethyl ester | A cell-permeable, quinolone-based fluorescent probe used as a zinc indicat… | 500 µg | 15133-500 | More Info |
| Ziprasidone-d8 | An internal standard for the quantification of ziprasidone by GC- or LC-MS | 1 mg | 30737-1 | More Info |
| Ziprasidone (hydrochloride hydrate) | An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… | 10 mg | 15031-10 | More Info |
| Ziprasidone (hydrochloride hydrate) | An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… | 25 mg | 15031-25 | More Info |
| Ziprasidone (hydrochloride hydrate) | An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… | 5 mg | 15031-5 | More Info |
| Ziprasidone (hydrochloride hydrate) | An atypical antipsychotic; an agonist of 5-HT1A receptors (EC50 = 36.31 nM… | 50 mg | 15031-50 | More Info |
| Ziptide (trifluoroacetate salt) | A peptide substrate for various serine / threonine protein kinases; has be… | 1 mg | 37466-1 | More Info |
| Ziptide (trifluoroacetate salt) | A peptide substrate for various serine / threonine protein kinases; has be… | 10 mg | 37466-10 | More Info |
| Ziptide (trifluoroacetate salt) | A peptide substrate for various serine / threonine protein kinases; has be… | 25 mg | 37466-25 | More Info |
| Ziptide (trifluoroacetate salt) | A peptide substrate for various serine / threonine protein kinases; has be… | 5 mg | 37466-5 | More Info |
| Ziyuglycoside I | A triterpenoid saponin with diverse biological activities; increases the s… | 1 mg | 37320-1 | More Info |
| Ziyuglycoside I | A triterpenoid saponin with diverse biological activities; increases the s… | 10 mg | 37320-10 | More Info |
| Ziyuglycoside I | A triterpenoid saponin with diverse biological activities; increases the s… | 25 mg | 37320-25 | More Info |
| Ziyuglycoside I | A triterpenoid saponin with diverse biological activities; increases the s… | 5 mg | 37320-5 | More Info |
| Ziyuglycoside II | A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… | 10 mg | 40831-10 | More Info |
| Ziyuglycoside II | A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… | 25 mg | 40831-25 | More Info |
| Ziyuglycoside II | A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… | 5 mg | 40831-5 | More Info |
| Ziyuglycoside II | A glycoside with diverse biological activities; cytotoxic to SMMC-7721, PC… | 50 mg | 40831-50 | More Info |
| ZK 159222 | An antagonist of the vitamin D receptor; inhibits VDR-mediated target gene… | 500 µg | 9001925-500 | More Info |
| ZK 824859 | An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… | 10 mg | 37789-10 | More Info |
| ZK 824859 | An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… | 25 mg | 37789-25 | More Info |
| ZK 824859 | An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… | 5 mg | 37789-5 | More Info |
| ZK 824859 | An inhibitor of uPA (IC50s = 79 and 410 nM for the human and mouse protein… | 50 mg | 37789-50 | More Info |
| ZK 756326 (hydrochloride) | A non-peptide agonist of CCR8; inhibits binding of CCL1 to human CCR8 (IC5… | 10 mg | 28454-10 | More Info |
| ZK 756326 (hydrochloride) | A non-peptide agonist of CCR8; inhibits binding of CCL1 to human CCR8 (IC5… | 25 mg | 28454-25 | More Info |
| ZK 756326 (hydrochloride) | A non-peptide agonist of CCR8; inhibits binding of CCL1 to human CCR8 (IC5… | 5 mg | 28454-5 | More Info |
| ZK118182 isopropyl ester | A prodrug formulation of a potent DP-receptor agonist that is designed to… | 100 µg | 13673-100 | More Info |
| ZK118182 isopropyl ester | A prodrug formulation of a potent DP-receptor agonist that is designed to… | 500 µg | 13673-500 | More Info |
| ZL006 | An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… | 10 mg | 34147-10 | More Info |
| ZL006 | An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… | 25 mg | 34147-25 | More Info |
| ZL006 | An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… | 5 mg | 34147-5 | More Info |
| ZL006 | An nNOS / PSD-95 interaction inhibitor; inhibits NMDA-induced lactate dehy… | 50 mg | 34147-50 | More Info |
| ZL0420 | A BRD4 inhibitor; inhibits BD1 and BD2 in BRD4 (IC50s = 27 and 32 nM, resp… | 10 mg | 30741-10 | More Info |
| ZL0420 | A BRD4 inhibitor; inhibits BD1 and BD2 in BRD4 (IC50s = 27 and 32 nM, resp… | 25 mg | 30741-25 | More Info |
| ZL0420 | A BRD4 inhibitor; inhibits BD1 and BD2 in BRD4 (IC50s = 27 and 32 nM, resp… | 5 mg | 30741-5 | More Info |
| Z-(L-Arg)-AMC (hydrochloride) | A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… | 10 mg | 30797-10 | More Info |
| Z-(L-Arg)-AMC (hydrochloride) | A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… | 100 mg | 30797-100 | More Info |
| Z-(L-Arg)-AMC (hydrochloride) | A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… | 25 mg | 30797-25 | More Info |
| Z-(L-Arg)-AMC (hydrochloride) | A fluorogenic substrate for trypsin, cathepsin B, and cathepsin H; AMC is… | 50 mg | 30797-50 | More Info |
| ZLD1039 | An inhibitor of EZH2 (IC50 = 5.6 nM); selective for EZH2 over EZH1 (IC50 =… | 1 mg | 19218-1 | More Info |
| ZLD1039 | An inhibitor of EZH2 (IC50 = 5.6 nM); selective for EZH2 over EZH1 (IC50 =… | 5 mg | 19218-5 | More Info |
| Z-Leu-Leu-Leu-B(OH)2 | A proteasome inhibitor with diverse biological activities; inhibits LPS-in… | 1 mg | 10008311-1 | More Info |
| Z-Leu-Leu-Leu-B(OH)2 | A proteasome inhibitor with diverse biological activities; inhibits LPS-in… | 200 µg | 10008311-200 | More Info |
| (Z)-Ligustilide | A phthalide with diverse biological activities; inhibits autophagy and res… | 100 mg | 26908-100 | More Info |
| (Z)-Ligustilide | A phthalide with diverse biological activities; inhibits autophagy and res… | 25 mg | 26908-25 | More Info |
| (Z)-Ligustilide | A phthalide with diverse biological activities; inhibits autophagy and res… | 50 mg | 26908-50 | More Info |
| 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 |
| 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 |
| 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 |
| 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 |
| Z-LLE-AMC | A fluorogenic substrate for the caspase-like post-glutamate peptide hydrol… | 1 mg | 10008117-1 | More Info |
| Z-LLE-AMC | A fluorogenic substrate for the caspase-like post-glutamate peptide hydrol… | 10 mg | 10008117-10 | More Info |
| Z-LLE-AMC | A fluorogenic substrate for the caspase-like post-glutamate peptide hydrol… | 5 mg | 10008117-5 | More Info |
| Z-LLL-AMC | A fluorogenic substrate for the chymotrypsin-like activity of the 26S prot… | 1 mg | 10008118-1 | More Info |
| Z-LLL-AMC | A fluorogenic substrate for the chymotrypsin-like activity of the 26S prot… | 10 mg | 10008118-10 | More Info |
| Z-LLL-AMC | A fluorogenic substrate for the chymotrypsin-like activity of the 26S prot… | 5 mg | 10008118-5 | More Info |
| ZLN005 | A small molecule that stimulates the expression of PGC-1α and downst… | 10 mg | 14121-10 | More Info |
| ZLN005 | A small molecule that stimulates the expression of PGC-1α and downst… | 25 mg | 14121-25 | More Info |
| ZLN005 | A small molecule that stimulates the expression of PGC-1α and downst… | 5 mg | 14121-5 | More Info |
| ZLN005 | A small molecule that stimulates the expression of PGC-1α and downst… | 50 mg | 14121-50 | More Info |
| ZLN024 | An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… | 10 mg | 21644-10 | More Info |
| ZLN024 | An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… | 25 mg | 21644-25 | More Info |
| ZLN024 | An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… | 5 mg | 21644-5 | More Info |
| ZLN024 | An allosteric activator of AMPK heterotrimers (EC50s = 0.42 and 0.95 &micr… | 50 mg | 21644-50 | More Info |
| ZLN005 (hydrochloride) | A small molecule that stimulates the expression of PGC-1α and downst… | 10 mg | 9002449-10 | More Info |
| ZLN005 (hydrochloride) | A small molecule that stimulates the expression of PGC-1α and downst… | 25 mg | 9002449-25 | More Info |
| ZLN005 (hydrochloride) | A small molecule that stimulates the expression of PGC-1α and downst… | 5 mg | 9002449-5 | More Info |
| ZLN005 (hydrochloride) | A small molecule that stimulates the expression of PGC-1α and downst… | 50 mg | 9002449-50 | More Info |
| 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 |
| 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 |
| 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 |
| Z-LRGG-AMC (trifluoroacetate salt) | A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… | 10 mg | 26641-10 | More Info |
| Z-LRGG-AMC (trifluoroacetate salt) | A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… | 25 mg | 26641-25 | More Info |
| Z-LRGG-AMC (trifluoroacetate salt) | A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… | 5 mg | 26641-5 | More Info |
| Z-LRGG-AMC (trifluoroacetate salt) | A fluorogenic substrate for isopeptidase T; AMC is released upon enzymatic… | 50 mg | 26641-50 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 10 mg | 31485-10 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 25 mg | 31485-25 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 5 mg | 31485-5 | More Info |
| ZLY032 | A dual agonist of FFAR1 / GPR40 (EC50 = 68 nM in a FLIPR assay) and PPAR&d… | 50 mg | 31485-50 | More Info |
| ZLY28 | An FXR agonist and inhibitor of FABP1; selectively induces reporter gene e… | 1 mg | 38864-1 | More Info |
| ZLY28 | An FXR agonist and inhibitor of FABP1; selectively induces reporter gene e… | 5 mg | 38864-5 | More Info |
| Z-Lys-OBzl (benzenesulfonate) | An amino acid-containing building block | 1 g | 30916-1 | More Info |
| Z-Lys-OBzl (benzenesulfonate) | An amino acid-containing building block | 500 mg | 30916-500 | More Info |
| Z-Lys-OH | An amino acid building block; has been used in the synthesis of peptidomim… | 1 g | 30460-1 | More Info |
| Z-Lys-OH | An amino acid building block; has been used in the synthesis of peptidomim… | 10 g | 30460-10 | More Info |
| Z-Lys-OH | An amino acid building block; has been used in the synthesis of peptidomim… | 5 g | 30460-5 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 1 g | 30804-1 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 100 mg | 30804-100 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 250 mg | 30804-250 | More Info |
| Z-Lys-OMe (hydrochloride) | A synthetic intermediate; has been used in the synthesis of peptide enzyme… | 500 mg | 30804-500 | More Info |
| ZM 241385 | A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… | 1 mg | 20447-1 | More Info |
| ZM 241385 | A potent, selective antagonist of A2A adenosine receptors (pIC50 = 9.52 fo… | 10 mg | 20447-10 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
Sales: sales@caymanchem.com
http://www.caymanchem.com
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