CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 645 of 649
Non-Antibody Products
Page 645 of 649
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Zileuton-d4 | An internal standard for the quantification of zileuton by GC- or LC-MS | 500 µg | 26761-500 | More Info |
| Zilpaterol-d7 | An internal standard for the quantification of zilpaterol by GC- or LC-MS, | 1 mg | 22903-1 | More Info |
| Zilpaterol (hydrochloride) | A β-adrenergic receptor agonist that putatively through activation of… | 1 mg | 16484-1 | More Info |
| Zilpaterol (hydrochloride) | A β-adrenergic receptor agonist that putatively through activation of… | 10 mg | 16484-10 | More Info |
| Zilpaterol (hydrochloride) | A β-adrenergic receptor agonist that putatively through activation of… | 5 mg | 16484-5 | More Info |
| ZINC00881524 | A ROCK inhibitor; decreases levels of ROCK1 in T47D and CAMA-1 breast canc… | 10 mg | 30788-10 | More Info |
| ZINC00881524 | A ROCK inhibitor; decreases levels of ROCK1 in T47D and CAMA-1 breast canc… | 100 mg | 30788-100 | More Info |
| ZINC00881524 | A ROCK inhibitor; decreases levels of ROCK1 in T47D and CAMA-1 breast canc… | 5 mg | 30788-5 | More Info |
| ZINC00881524 | A ROCK inhibitor; decreases levels of ROCK1 in T47D and CAMA-1 breast canc… | 50 mg | 30788-50 | More Info |
| Zinc Protoporphyrin-9 | A competitive inhibitor of heme oxygenase that also inhibits soluble guany… | 10 mg | 14483-10 | More Info |
| Zinc Protoporphyrin-9 | A competitive inhibitor of heme oxygenase that also inhibits soluble guany… | 100 mg | 14483-100 | More Info |
| Zinc Protoporphyrin-9 | A competitive inhibitor of heme oxygenase that also inhibits soluble guany… | 25 mg | 14483-25 | More Info |
| Zinc Protoporphyrin-9 | A competitive inhibitor of heme oxygenase that also inhibits soluble guany… | 50 mg | 14483-50 | More Info |
| Zinc Pyrithione | A coordination complex of zinc and pyrithione that has antimicrobial and a… | 100 mg | 29154-100 | More Info |
| Zingerone | A phenolic ketone; scavenges DPPH radicals in a cell-free assay (EC50 = 41… | 100 g | 24909-100 | More Info |
| Zingerone | A phenolic ketone; scavenges DPPH radicals in a cell-free assay (EC50 = 41… | 25 g | 24909-25 | More Info |
| Zingerone | A phenolic ketone; scavenges DPPH radicals in a cell-free assay (EC50 = 41… | 250 g | 24909-250 | More Info |
| Zingerone | A phenolic ketone; scavenges DPPH radicals in a cell-free assay (EC50 = 41… | 50 g | 24909-50 | More Info |
| Zingibroside R1 | A triterpene saponin and an active metabolite of ginsenoside Ro; cytotoxic… | 1 mg | 34130-1 | More Info |
| Zingibroside R1 | A triterpene saponin and an active metabolite of ginsenoside Ro; cytotoxic… | 10 mg | 34130-10 | More Info |
| Zingibroside R1 | A triterpene saponin and an active metabolite of ginsenoside Ro; cytotoxic… | 25 mg | 34130-25 | More Info |
| 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 |
| 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 |
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
Return to Profile