CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 856 of 865
Non-Antibody Products
Page 856 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Yunaconitine | A diterpenoid alkaloid with diverse biological activities; active against… | 10 mg | 34127-10 | More Info |
| Yunaconitine | A diterpenoid alkaloid with diverse biological activities; active against… | 25 mg | 34127-25 | More Info |
| Yunaconitine | A diterpenoid alkaloid with diverse biological activities; active against… | 5 mg | 34127-5 | More Info |
| YVAD-CHO (trifluoroacetate salt) | A caspase-1 / ICE inhibitor; prevents ICE-like and CPP32-like proteinase a… | 1 mg | 27420-1 | More Info |
| YVAD-CHO (trifluoroacetate salt) | A caspase-1 / ICE inhibitor; prevents ICE-like and CPP32-like proteinase a… | 5 mg | 27420-5 | More Info |
| YW1128 | An inhibitor of Wnt signaling (IC50 = 4.1 nM); decreases lipid accumulatio… | 1 mg | 27450-1 | More Info |
| YW1128 | An inhibitor of Wnt signaling (IC50 = 4.1 nM); decreases lipid accumulatio… | 10 mg | 27450-10 | More Info |
| YW1128 | An inhibitor of Wnt signaling (IC50 = 4.1 nM); decreases lipid accumulatio… | 5 mg | 27450-5 | More Info |
| YW1159 | An inhibitor of Wnt signaling (IC50 = 1.2 nM); not cytotoxic to HEK293 cel… | 1 mg | 27451-1 | More Info |
| YW1159 | An inhibitor of Wnt signaling (IC50 = 1.2 nM); not cytotoxic to HEK293 cel… | 10 mg | 27451-10 | More Info |
| YW1159 | An inhibitor of Wnt signaling (IC50 = 1.2 nM); not cytotoxic to HEK293 cel… | 5 mg | 27451-5 | More Info |
| YYA-021 | A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… | 1 mg | 22915-1 | More Info |
| YYA-021 | A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… | 10 mg | 22915-10 | More Info |
| YYA-021 | A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… | 25 mg | 22915-25 | More Info |
| YYA-021 | A small molecule CD4 mimetic; inhibits gp120 and CD4 interaction, preventi… | 5 mg | 22915-5 | More Info |
| YZ9 | A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… | 10 mg | 15352-10 | More Info |
| YZ9 | A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… | 100 mg | 15352-100 | More Info |
| YZ9 | A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… | 5 mg | 15352-5 | More Info |
| YZ9 | A potent inhibitor of the glycolysis enzyme PFKFB3, with an IC50 value of… | 50 mg | 15352-50 | More Info |
| Z944 | A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… | 1 mg | 27679-1 | More Info |
| Z944 | A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… | 10 mg | 27679-10 | More Info |
| Z944 | A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… | 25 mg | 27679-25 | More Info |
| Z944 | A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human… | 5 mg | 27679-5 | More Info |
| Z-AEVD-FMK | An irreversible inhibitor of caspase-10 and related caspases that at 10 &m… | 1 mg | 14987-1 | More Info |
| Z-AEVD-FMK | An irreversible inhibitor of caspase-10 and related caspases that at 10 &m… | 5 mg | 14987-5 | More Info |
| Z-AEVD-FMK | An irreversible inhibitor of caspase-10 and related caspases that at 10 &m… | 500 µg | 14987-500 | More Info |
| Zafirlukast | A CysLT1 receptor antagonist (IC50 = 0.014 µM in a cell-based calciu… | 10 mg | 10008282-10 | More Info |
| Zafirlukast | A CysLT1 receptor antagonist (IC50 = 0.014 µM in a cell-based calciu… | 100 mg | 10008282-100 | More Info |
| Zafirlukast | A CysLT1 receptor antagonist (IC50 = 0.014 µM in a cell-based calciu… | 1000 mg | 10008282-1 | More Info |
| Zafirlukast | A CysLT1 receptor antagonist (IC50 = 0.014 µM in a cell-based calciu… | 500 mg | 10008282-500 | More Info |
| (Z-Ala-Ala-Ala-Ala)2Rh110 | A sensitive fluorogenic elastase substrate that is selectively cleaved by… | 1 mg | 11675-1 | More Info |
| (Z-Ala-Ala-Ala-Ala)2Rh110 | A sensitive fluorogenic elastase substrate that is selectively cleaved by… | 10 mg | 11675-10 | More Info |
| (Z-Ala-Ala-Ala-Ala)2Rh110 | A sensitive fluorogenic elastase substrate that is selectively cleaved by… | 5 mg | 11675-5 | More Info |
| Zalcitabine | A NRTI; reduces the replication of laboratory-adapted and clinical isolate… | 100 mg | 16019-100 | More Info |
| Zalcitabine | A NRTI; reduces the replication of laboratory-adapted and clinical isolate… | 25 mg | 16019-25 | More Info |
| Zalcitabine | A NRTI; reduces the replication of laboratory-adapted and clinical isolate… | 250 mg | 16019-250 | More Info |
| Zalcitabine | A NRTI; reduces the replication of laboratory-adapted and clinical isolate… | 500 mg | 16019-500 | More Info |
| Zaltoprofen | An NSAID that displays slight preferential inhibition for COX-2 (IC50s = 1… | 10 mg | 14662-10 | More Info |
| Zaltoprofen | An NSAID that displays slight preferential inhibition for COX-2 (IC50s = 1… | 100 mg | 14662-100 | More Info |
| Zaltoprofen | An NSAID that displays slight preferential inhibition for COX-2 (IC50s = 1… | 250 mg | 14662-250 | More Info |
| Zaltoprofen | An NSAID that displays slight preferential inhibition for COX-2 (IC50s = 1… | 50 mg | 14662-50 | More Info |
| Zamifenacin (fumarate) | An antagonist of M3 muscarinic acetylcholine receptors (Ki = 10 nM for the… | 1 mg | 32848-1 | More Info |
| Zamifenacin (fumarate) | An antagonist of M3 muscarinic acetylcholine receptors (Ki = 10 nM for the… | 10 mg | 32848-10 | More Info |
| Zamifenacin (fumarate) | An antagonist of M3 muscarinic acetylcholine receptors (Ki = 10 nM for the… | 5 mg | 32848-5 | More Info |
| Zanamivir | An inhibitor of influenza neuraminidase; inhibits neuraminidase activity i… | 1 mg | 15123-1 | More Info |
| Zanamivir | An inhibitor of influenza neuraminidase; inhibits neuraminidase activity i… | 10 mg | 15123-10 | More Info |
| Zanamivir | An inhibitor of influenza neuraminidase; inhibits neuraminidase activity i… | 25 mg | 15123-25 | More Info |
| Zanamivir | An inhibitor of influenza neuraminidase; inhibits neuraminidase activity i… | 5 mg | 15123-5 | More Info |
| Zanamivir-13C,15N2 (hydrate) | An internal standard for the quantification of zanamivir by GC- or LC-MS | 250 µg | 30733-250 | More Info |
| Zanubrutinib | A potent and covalent BTK inhibitor (IC50 = 0.3 nM); selective for BTK ove… | 1 mg | 28924-1 | More Info |
| Zanubrutinib | A potent and covalent BTK inhibitor (IC50 = 0.3 nM); selective for BTK ove… | 10 mg | 28924-10 | More Info |
| Zanubrutinib | A potent and covalent BTK inhibitor (IC50 = 0.3 nM); selective for BTK ove… | 25 mg | 28924-25 | More Info |
| Zanubrutinib | A potent and covalent BTK inhibitor (IC50 = 0.3 nM); selective for BTK ove… | 5 mg | 28924-5 | More Info |
| Zapnometinib | A MEK inhibitor (IC50 = 5.73 nM) and an active metabolite of CI-1040; redu… | 10 mg | 38517-10 | More Info |
| Zapnometinib | A MEK inhibitor (IC50 = 5.73 nM) and an active metabolite of CI-1040; redu… | 25 mg | 38517-25 | More Info |
| Zapnometinib | A MEK inhibitor (IC50 = 5.73 nM) and an active metabolite of CI-1040; redu… | 5 mg | 38517-5 | More Info |
| Zapnometinib | A MEK inhibitor (IC50 = 5.73 nM) and an active metabolite of CI-1040; redu… | 50 mg | 38517-50 | More Info |
| Zaprinast | A cGMP phosphodiesterase inhibitor (IC50s = 0.5-0.76 and 0.15 µM for… | 10 mg | 10010421-10 | More Info |
| Zaprinast | A cGMP phosphodiesterase inhibitor (IC50s = 0.5-0.76 and 0.15 µM for… | 100 mg | 10010421-100 | More Info |
| Zaprinast | A cGMP phosphodiesterase inhibitor (IC50s = 0.5-0.76 and 0.15 µM for… | 250 mg | 10010421-250 | More Info |
| Zaprinast | A cGMP phosphodiesterase inhibitor (IC50s = 0.5-0.76 and 0.15 µM for… | 50 mg | 10010421-50 | More Info |
| Zaragozic Acid A | A reversible competitive inhibitor of squalene synthase (Ki = 78 pM in vit… | 1 mg | 17452-1 | More Info |
| Zaragozic Acid A | A reversible competitive inhibitor of squalene synthase (Ki = 78 pM in vit… | 5 mg | 17452-5 | More Info |
| Zardaverine | A dual inhibitor of PDE3 and PDE4 (IC50s = 0.617 and 1.738 µM, respe… | 1 mg | 29685-1 | More Info |
| Zardaverine | A dual inhibitor of PDE3 and PDE4 (IC50s = 0.617 and 1.738 µM, respe… | 10 mg | 29685-10 | More Info |
| Zardaverine | A dual inhibitor of PDE3 and PDE4 (IC50s = 0.617 and 1.738 µM, respe… | 25 mg | 29685-25 | More Info |
| Zardaverine | A dual inhibitor of PDE3 and PDE4 (IC50s = 0.617 and 1.738 µM, respe… | 5 mg | 29685-5 | More Info |
| Z-Asp-CH2-DCB | A pan-caspase inhibitor that blocks apoptosis, prevents the production of… | 10 mg | 15143-10 | More Info |
| Z-Asp-CH2-DCB | A pan-caspase inhibitor that blocks apoptosis, prevents the production of… | 25 mg | 15143-25 | More Info |
| Z-Asp-CH2-DCB | A pan-caspase inhibitor that blocks apoptosis, prevents the production of… | 5 mg | 15143-5 | More Info |
| Z-Asp-CH2-DCB | A pan-caspase inhibitor that blocks apoptosis, prevents the production of… | 50 mg | 15143-50 | More Info |
| Zatebradine (hydrochloride) | Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… | 10 mg | 18608-10 | More Info |
| Zatebradine (hydrochloride) | Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… | 25 mg | 18608-25 | More Info |
| Zatebradine (hydrochloride) | Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… | 5 mg | 18608-5 | More Info |
| Zatebradine (hydrochloride) | Blocks If currents through HCN channels in sinoatrial node cells (IC50s =… | 50 mg | 18608-50 | 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
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