CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 189 of 859
Non-Antibody Products
Page 189 of 859
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| CP 226,269 | A dopamine D4 receptor agonist; induces calcium flux in HEK293 cells co-ex… | 5 mg | 36493-5 | More Info |
| CP 316,819 | An inhibitor of glycogen phosphorylase A (IC50 = 40 nM for the human liver… | 1 mg | 32856-1 | More Info |
| CP 316,819 | An inhibitor of glycogen phosphorylase A (IC50 = 40 nM for the human liver… | 5 mg | 32856-5 | More Info |
| CP 346,086 | An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… | 1 mg | 39156-1 | More Info |
| CP 346,086 | An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… | 10 mg | 39156-10 | More Info |
| CP 346,086 | An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… | 25 mg | 39156-25 | More Info |
| CP 346,086 | An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… | 5 mg | 39156-5 | More Info |
| CP 376,395 | A CRF1 antagonist (IC50 = 5.1 nM); inhibits adenylate cyclase activity sti… | 1 mg | 29188-1 | More Info |
| CP 376,395 | A CRF1 antagonist (IC50 = 5.1 nM); inhibits adenylate cyclase activity sti… | 10 mg | 29188-10 | More Info |
| CP 376,395 | A CRF1 antagonist (IC50 = 5.1 nM); inhibits adenylate cyclase activity sti… | 5 mg | 29188-5 | More Info |
| CP 424,174 | An inhibitor of stimulus-coupled IL-1β post-translational processing;… | 1 mg | 29675-1 | More Info |
| CP 424,174 | An inhibitor of stimulus-coupled IL-1β post-translational processing;… | 10 mg | 29675-10 | More Info |
| CP 424,174 | An inhibitor of stimulus-coupled IL-1β post-translational processing;… | 25 mg | 29675-25 | More Info |
| CP 424,174 | An inhibitor of stimulus-coupled IL-1β post-translational processing;… | 5 mg | 29675-5 | More Info |
| CP 466,722 | An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… | 1 mg | 25417-1 | More Info |
| CP 466,722 | An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… | 10 mg | 25417-10 | More Info |
| CP 466,722 | An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… | 25 mg | 25417-25 | More Info |
| CP 466,722 | An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… | 5 mg | 25417-5 | More Info |
| CP 471,474 | A broad-spectrum MMP inhibitor (IC50s = 0.7, 16, 13, and 0.9 nM for MMP-2,… | 1 mg | 29442-1 | More Info |
| CP 471,474 | A broad-spectrum MMP inhibitor (IC50s = 0.7, 16, 13, and 0.9 nM for MMP-2,… | 10 mg | 29442-10 | More Info |
| CP 471,474 | A broad-spectrum MMP inhibitor (IC50s = 0.7, 16, 13, and 0.9 nM for MMP-2,… | 5 mg | 29442-5 | More Info |
| CP 544,326 | A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… | 1 mg | 22945-1 | More Info |
| CP 544,326 | A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… | 10 mg | 22945-10 | More Info |
| CP 544,326 | A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… | 25 mg | 22945-25 | More Info |
| CP 544,326 | A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… | 5 mg | 22945-5 | More Info |
| CP 547,632 | A potent inhibitor of VEGFR2 and bFGF (IC50s = 11 and 9 nM, respectively);… | 1 mg | 21773-1 | More Info |
| CP 547,632 | A potent inhibitor of VEGFR2 and bFGF (IC50s = 11 and 9 nM, respectively);… | 5 mg | 21773-5 | More Info |
| CP 547,632 | A potent inhibitor of VEGFR2 and bFGF (IC50s = 11 and 9 nM, respectively);… | 500 µg | 21773-500 | More Info |
| CP 640,186 | An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… | 1 mg | 17691-1 | More Info |
| CP 640,186 | An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… | 10 mg | 17691-10 | More Info |
| CP 640,186 | An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… | 25 mg | 17691-25 | More Info |
| CP 640,186 | An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… | 5 mg | 17691-5 | More Info |
| CP 671,305 | A potent PDE4D inhibitor (IC50 = 3 nM); selective for PDE4D over PDE4A, -B… | 1 mg | 26743-1 | More Info |
| CP 671,305 | A potent PDE4D inhibitor (IC50 = 3 nM); selective for PDE4D over PDE4A, -B… | 10 mg | 26743-10 | More Info |
| CP 671,305 | A potent PDE4D inhibitor (IC50 = 3 nM); selective for PDE4D over PDE4A, -B… | 5 mg | 26743-5 | More Info |
| CP 673,451 | A selective inhibitor of PDGFRβ and PDGFRα kinases (IC50s = 1 a… | 1 mg | 19170-1 | More Info |
| CP 673,451 | A selective inhibitor of PDGFRβ and PDGFRα kinases (IC50s = 1 a… | 10 mg | 19170-10 | More Info |
| CP 673,451 | A selective inhibitor of PDGFRβ and PDGFRα kinases (IC50s = 1 a… | 5 mg | 19170-5 | More Info |
| CP 724,714 | A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… | 1 mg | 19172-1 | More Info |
| CP 724,714 | A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… | 10 mg | 19172-10 | More Info |
| CP 724,714 | A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… | 25 mg | 19172-25 | More Info |
| CP 724,714 | A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… | 5 mg | 19172-5 | More Info |
| CP 775,146 | A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… | 1 mg | 28290-1 | More Info |
| CP 775,146 | A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… | 10 mg | 28290-10 | More Info |
| CP 775,146 | A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… | 25 mg | 28290-25 | More Info |
| CP 775,146 | A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… | 5 mg | 28290-5 | More Info |
| CP 80,633 | A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… | 1 mg | 13183-1 | More Info |
| CP 80,633 | A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… | 10 mg | 13183-10 | More Info |
| CP 80,633 | A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… | 5 mg | 13183-5 | More Info |
| CP 80,633 | A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… | 500 µg | 13183-500 | More Info |
| CP 809,101 | A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… | 10 mg | 24214-10 | More Info |
| CP 809,101 | A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… | 25 mg | 24214-25 | More Info |
| CP 809,101 | A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… | 5 mg | 24214-5 | More Info |
| CP 809,101 | A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… | 50 mg | 24214-50 | More Info |
| CP 91,149 | An inhibitor of LGPa, MGPa, and MGPb (IC50s = 0.13, 0.2, and 0.3 µM,… | 10 mg | 17709-10 | More Info |
| CP 91,149 | An inhibitor of LGPa, MGPa, and MGPb (IC50s = 0.13, 0.2, and 0.3 µM,… | 25 mg | 17709-25 | More Info |
| CP 91,149 | An inhibitor of LGPa, MGPa, and MGPb (IC50s = 0.13, 0.2, and 0.3 µM,… | 5 mg | 17709-5 | More Info |
| CP102 | An iron chelator; decreases hepatic total non-heme and ferritin-stored iro… | 1 mg | 33324-1 | More Info |
| CP102 | An iron chelator; decreases hepatic total non-heme and ferritin-stored iro… | 10 mg | 33324-10 | More Info |
| CP102 | An iron chelator; decreases hepatic total non-heme and ferritin-stored iro… | 5 mg | 33324-5 | More Info |
| CP21 | An iron chelator; active against P. falciparum at 10 and 100 µM; inh… | 1 mg | 33318-1 | More Info |
| CP21 | An iron chelator; active against P. falciparum at 10 and 100 µM; inh… | 10 mg | 33318-10 | More Info |
| CP21 | An iron chelator; active against P. falciparum at 10 and 100 µM; inh… | 25 mg | 33318-25 | More Info |
| CP21 | An iron chelator; active against P. falciparum at 10 and 100 µM; inh… | 5 mg | 33318-5 | More Info |
| CP94 | An iron chelator; enhances protoporphyrin IX photobleaching and decreases… | 1 mg | 33323-1 | More Info |
| CP94 | An iron chelator; enhances protoporphyrin IX photobleaching and decreases… | 10 mg | 33323-10 | More Info |
| CP94 | An iron chelator; enhances protoporphyrin IX photobleaching and decreases… | 25 mg | 33323-25 | More Info |
| CP94 | An iron chelator; enhances protoporphyrin IX photobleaching and decreases… | 5 mg | 33323-5 | More Info |
| CP 105,696 | A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… | 1 mg | 17620-1 | More Info |
| CP 105,696 | A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… | 10 mg | 17620-10 | More Info |
| CP 105,696 | A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… | 25 mg | 17620-25 | More Info |
| CP 105,696 | A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… | 5 mg | 17620-5 | More Info |
| CPCCOEt | A low affinity, selective, non-competitive antagonist of mGluR1b (IC50 = 6… | 1 mg | 21486-1 | More Info |
| CPCCOEt | A low affinity, selective, non-competitive antagonist of mGluR1b (IC50 = 6… | 10 mg | 21486-10 | More Info |
| CPCCOEt | A low affinity, selective, non-competitive antagonist of mGluR1b (IC50 = 6… | 5 mg | 21486-5 | 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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