CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 828 of 865
Non-Antibody Products
Page 828 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| U-0124 | An inactive analog of U-0126; has been used as a negative control for the… | 500 µg | 34871-500 | More Info |
| U-0126 | A non ATP-competitive MEK inhibitor (IC50 = 72 and 58 nM for MEK1 and MEK2… | 1 mg | 70970-1 | More Info |
| U-0126 | A non ATP-competitive MEK inhibitor (IC50 = 72 and 58 nM for MEK1 and MEK2… | 10 mg | 70970-10 | More Info |
| U-0126 | A non ATP-competitive MEK inhibitor (IC50 = 72 and 58 nM for MEK1 and MEK2… | 25 mg | 70970-25 | More Info |
| U-0126 | A non ATP-competitive MEK inhibitor (IC50 = 72 and 58 nM for MEK1 and MEK2… | 5 mg | 70970-5 | More Info |
| U-0521 | An inhibitor of COMT (Ki = 7.8 µM for the rat liver enzyme) and tyro… | 100 mg | 36314-100 | More Info |
| U-0521 | An inhibitor of COMT (Ki = 7.8 µM for the rat liver enzyme) and tyro… | 25 mg | 36314-25 | More Info |
| U-0521 | An inhibitor of COMT (Ki = 7.8 µM for the rat liver enzyme) and tyro… | 50 mg | 36314-50 | More Info |
| U-104 | A ureido-sulfonamide inhibitor of carbonic anhydrases IX and CAXII (Kis =… | 10 mg | 16717-10 | More Info |
| U-104 | A ureido-sulfonamide inhibitor of carbonic anhydrases IX and CAXII (Kis =… | 25 mg | 16717-25 | More Info |
| U-104 | A ureido-sulfonamide inhibitor of carbonic anhydrases IX and CAXII (Kis =… | 5 mg | 16717-5 | More Info |
| U-104 | A ureido-sulfonamide inhibitor of carbonic anhydrases IX and CAXII (Kis =… | 50 mg | 16717-50 | More Info |
| U-44069 | A stable analog of PGH2 and a TP receptor agonist; stimulates shape change… | 1 mg | 16440-1 | More Info |
| U-44069 | A stable analog of PGH2 and a TP receptor agonist; stimulates shape change… | 10 mg | 16440-10 | More Info |
| U-44069 | A stable analog of PGH2 and a TP receptor agonist; stimulates shape change… | 5 mg | 16440-5 | More Info |
| U-46619 | TXA2 receptor agonist; causes platelet shape change (EC50 ~6 nM) and aggre… | 1 mg | 16450-1 | More Info |
| U-46619 | TXA2 receptor agonist; causes platelet shape change (EC50 ~6 nM) and aggre… | 10 mg | 16450-10 | More Info |
| U-46619 | TXA2 receptor agonist; causes platelet shape change (EC50 ~6 nM) and aggre… | 5 mg | 16450-5 | More Info |
| U-47109 | An analytical reference standard categorized as an opioid; intended for re… | 1 mg | 21663-1 | More Info |
| U-47109 | An analytical reference standard categorized as an opioid; intended for re… | 5 mg | 21663-5 | More Info |
| U-48520 | An analytical reference standard categorized as a utopioid; intended for r… | 1 mg | 26274-1 | More Info |
| U-48520 | An analytical reference standard categorized as a utopioid; intended for r… | 5 mg | 26274-5 | More Info |
| U-51605 | A stable analog of PGH2 that inhibits both PGI and TX synthases with more… | 1 mg | 16465-1 | More Info |
| U-51605 | A stable analog of PGH2 that inhibits both PGI and TX synthases with more… | 100 µg | 16465-100 | More Info |
| U-51605 | A stable analog of PGH2 that inhibits both PGI and TX synthases with more… | 500 µg | 16465-500 | More Info |
| U-69593 | An analytical reference standard categorized as an opioid; intended for re… | 1 mg | 13255-1 | More Info |
| U-69593 | An analytical reference standard categorized as an opioid; intended for re… | 5 mg | 13255-5 | More Info |
| U-73122 | An inhibitor of PLC-dependent processes by an undefined mechanism; inhibit… | 1 mg | 70740-1 | More Info |
| U-73122 | An inhibitor of PLC-dependent processes by an undefined mechanism; inhibit… | 10 mg | 70740-10 | More Info |
| U-73122 | An inhibitor of PLC-dependent processes by an undefined mechanism; inhibit… | 25 mg | 70740-25 | More Info |
| U-73122 | An inhibitor of PLC-dependent processes by an undefined mechanism; inhibit… | 5 mg | 70740-5 | More Info |
| U-73343 | An inactive analog of U-73122; can be used as a negative control | 1 mg | 17339-1 | More Info |
| U-73343 | An inactive analog of U-73122; can be used as a negative control | 10 mg | 17339-10 | More Info |
| U-73343 | An inactive analog of U-73122; can be used as a negative control | 25 mg | 17339-25 | More Info |
| U-73343 | An inactive analog of U-73122; can be used as a negative control | 5 mg | 17339-5 | More Info |
| U-75302 | A BLT1 receptor antagonist with a Ki value of 159 nM on guinea pig lung me… | 1 mg | 70705-1 | More Info |
| U-75302 | A BLT1 receptor antagonist with a Ki value of 159 nM on guinea pig lung me… | 100 µg | 70705-100 | More Info |
| U-75302 | A BLT1 receptor antagonist with a Ki value of 159 nM on guinea pig lung me… | 50 µg | 70705-50 | More Info |
| U-75302 | A BLT1 receptor antagonist with a Ki value of 159 nM on guinea pig lung me… | 500 µg | 70705-500 | More Info |
| U-93631 | A GABAA receptor ligand; accelerates decay of GABA-induced currents in HEK… | 100 mg | 26417-100 | More Info |
| U-93631 | A GABAA receptor ligand; accelerates decay of GABA-induced currents in HEK… | 25 mg | 26417-25 | More Info |
| U-93631 | A GABAA receptor ligand; accelerates decay of GABA-induced currents in HEK… | 50 mg | 26417-50 | More Info |
| U-18666A | A cell permeable drug that inhibits cholesterol trafficking from late endo… | 10 mg | 10009085-10 | More Info |
| U-18666A | A cell permeable drug that inhibits cholesterol trafficking from late endo… | 25 mg | 10009085-25 | More Info |
| U-18666A | A cell permeable drug that inhibits cholesterol trafficking from late endo… | 5 mg | 10009085-5 | More Info |
| U-18666A | A cell permeable drug that inhibits cholesterol trafficking from late endo… | 50 mg | 10009085-50 | More Info |
| U-92016A | A 5-HT1A receptor agonist (Ki = 0.4 nM); selective for 5-HT1A over 5-HT1D,… | 1 mg | 23807-1 | More Info |
| U-92016A | A 5-HT1A receptor agonist (Ki = 0.4 nM); selective for 5-HT1A over 5-HT1D,… | 10 mg | 23807-10 | More Info |
| U-92016A | A 5-HT1A receptor agonist (Ki = 0.4 nM); selective for 5-HT1A over 5-HT1D,… | 5 mg | 23807-5 | More Info |
| UAMC-3203 | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 1 mg | 26525-1 | More Info |
| UAMC-3203 | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 10 mg | 26525-10 | More Info |
| UAMC-3203 | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 25 mg | 26525-25 | More Info |
| UAMC-3203 | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 5 mg | 26525-5 | More Info |
| UAMC 0039 (hydrochloride) | A potent inhibitor of DPP-2 (IC50 = 0.48 nM); inhibits DPP-4 (IC50 = 165 m… | 1 mg | 15340-1 | More Info |
| UAMC 0039 (hydrochloride) | A potent inhibitor of DPP-2 (IC50 = 0.48 nM); inhibits DPP-4 (IC50 = 165 m… | 10 mg | 15340-10 | More Info |
| UAMC 0039 (hydrochloride) | A potent inhibitor of DPP-2 (IC50 = 0.48 nM); inhibits DPP-4 (IC50 = 165 m… | 5 mg | 15340-5 | More Info |
| UAMC-3203 (hydrochloride) | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 1 mg | 29346-1 | More Info |
| UAMC-3203 (hydrochloride) | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 10 mg | 29346-10 | More Info |
| UAMC-3203 (hydrochloride) | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 25 mg | 29346-25 | More Info |
| UAMC-3203 (hydrochloride) | A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in I… | 5 mg | 29346-5 | More Info |
| Ubiquinol | A reduced form of coenzyme Q10; traps lipid peroxyl radicals and inhibits… | 1 mg | 19677-1 | More Info |
| Ubiquinol | A reduced form of coenzyme Q10; traps lipid peroxyl radicals and inhibits… | 10 mg | 19677-10 | More Info |
| Ubiquinol | A reduced form of coenzyme Q10; traps lipid peroxyl radicals and inhibits… | 5 mg | 19677-5 | More Info |
| Ubiquinol | A reduced form of coenzyme Q10; traps lipid peroxyl radicals and inhibits… | 500 µg | 19677-500 | More Info |
| Ubiquitin (human, recombinant) | Source: Recombinant human ubiquitin expressed in E. coli • Amino acid… | 1 mg | 20487-1 | More Info |
| Ubiquitin (human, recombinant; His-tagged) | Source: Recombinant human N-terminal His-tagged ubiquitin expressed in E.… | 200 µg | 20488-200 | More Info |
| Ubiquitin Isopeptidase Inhibitor I | Induces caspase activation and apoptosis (IC50 = ~1.7 µM) through a… | 10 mg | 21006-10 | More Info |
| Ubiquitin Isopeptidase Inhibitor I | Induces caspase activation and apoptosis (IC50 = ~1.7 µM) through a… | 25 mg | 21006-25 | More Info |
| Ubiquitin Isopeptidase Inhibitor I | Induces caspase activation and apoptosis (IC50 = ~1.7 µM) through a… | 5 mg | 21006-5 | More Info |
| Ubiquitin Remnant (K-ε-GG) Immunoaffinity Sorbent | Consists of Cayman's diglycyl-lysine monoclonal antibody coupled to CNBr-a… | 400 µL | 34699-400 | More Info |
| UBP 301 | An antagonist of the kainate receptor, an ionotropic glutamate receptor (a… | 1 mg | 17597-1 | More Info |
| UBP 301 | An antagonist of the kainate receptor, an ionotropic glutamate receptor (a… | 10 mg | 17597-10 | More Info |
| UBP 301 | An antagonist of the kainate receptor, an ionotropic glutamate receptor (a… | 5 mg | 17597-5 | More Info |
| UBP 302 | An antagonist of GluR5 subunit-containing kainate receptors; inhibits kain… | 1 mg | 24309-1 | More Info |
| UBP 302 | An antagonist of GluR5 subunit-containing kainate receptors; inhibits kain… | 5 mg | 24309-5 | 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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