CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 190 of 859
Non-Antibody Products
Page 190 of 859
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| CP 47,497-C6-homolog | An analog of CP 47,497; intended for research and forensic applications | 1 mg | 9001448-1 | More Info |
| CP 47,497-C6-homolog | An analog of CP 47,497; intended for research and forensic applications | 5 mg | 9001448-5 | More Info |
| CP 47,497-C9-homolog | An analog of CP 47,497; intended for research and forensic applications | 1 mg | 9001449-1 | More Info |
| CP 47,497-C9-homolog | An analog of CP 47,497; intended for research and forensic applications | 5 mg | 9001449-5 | More Info |
| CP 47,497-C8-homolog C-8-hydroxy metabolite | A potential metabolite of CP 47,497-C8-homolog; intended for research and… | 1 mg | 9000773-1 | More Info |
| CP 47,497-C8-homolog C-8-hydroxy metabolite | A potential metabolite of CP 47,497-C8-homolog; intended for research and… | 100 µg | 9000773-100 | More Info |
| CP 47,497-C8-homolog C-8-hydroxy metabolite | A potential metabolite of CP 47,497-C8-homolog; intended for research and… | 500 µg | 9000773-500 | More Info |
| CpdA | A non-steroidal selective glucocorticoid receptor modulator; contradictory… | 10 mg | 21438-10 | More Info |
| CpdA | A non-steroidal selective glucocorticoid receptor modulator; contradictory… | 100 mg | 21438-100 | More Info |
| CpdA | A non-steroidal selective glucocorticoid receptor modulator; contradictory… | 25 mg | 21438-25 | More Info |
| CpdA | A non-steroidal selective glucocorticoid receptor modulator; contradictory… | 50 mg | 21438-50 | More Info |
| 8-cPeT NAD+ (sodium salt) | A derivative of NAD+; has been used in the screening of analog-sensitive P… | 800 µg | 38480-800 | More Info |
| (-)-CP 47,497 (exempt preparation) | A bicyclic CB analog with potent analgesic activity; comparable or more po… | 1 mg | 13218-1 | More Info |
| (-)-CP 47,497 (exempt preparation) | A bicyclic CB analog with potent analgesic activity; comparable or more po… | 5 mg | 13218-5 | More Info |
| (+)-CP 47,497 (exempt preparation) | A bicyclic CB analog with potent analgesic activity; comparable or more po… | 1 mg | 13219-1 | More Info |
| (+)-CP 47,497 (exempt preparation) | A bicyclic CB analog with potent analgesic activity; comparable or more po… | 5 mg | 13219-5 | More Info |
| CPHPC | An inhibitor of the protein-protein interaction between SAP and amyloid fi… | 10 mg | 75500-10 | More Info |
| CPHPC | An inhibitor of the protein-protein interaction between SAP and amyloid fi… | 5 mg | 75500-5 | More Info |
| CPHPC | An inhibitor of the protein-protein interaction between SAP and amyloid fi… | 50 mg | 75500-50 | More Info |
| 2C-P (hydrochloride) | A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… | 10 mg | 11696-10 | More Info |
| 2C-P (hydrochloride) | A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… | 5 mg | 11696-5 | More Info |
| 2C-P (hydrochloride) | A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… | 50 mg | 11696-50 | More Info |
| 3C-P (hydrochloride) | A phenethylamine with structural similarity to amphetamine and proscaline | 1 mg | 14954-1 | More Info |
| 3C-P (hydrochloride) | A phenethylamine with structural similarity to amphetamine and proscaline | 5 mg | 14954-5 | More Info |
| CP 100,356 (hydrochloride) | A P-glycoprotein inhibitor (IC50 = 0.5 µM); selective for P-gp over… | 1 mg | 32853-1 | More Info |
| CP 100,356 (hydrochloride) | A P-glycoprotein inhibitor (IC50 = 0.5 µM); selective for P-gp over… | 10 mg | 32853-10 | More Info |
| CP 100,356 (hydrochloride) | A P-glycoprotein inhibitor (IC50 = 0.5 µM); selective for P-gp over… | 5 mg | 32853-5 | More Info |
| CP 154,526 (hydrochloride) | An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… | 1 mg | 20732-1 | More Info |
| CP 154,526 (hydrochloride) | An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… | 10 mg | 20732-10 | More Info |
| CP 154,526 (hydrochloride) | An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… | 5 mg | 20732-5 | More Info |
| CP 154,526 (hydrochloride) | An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… | 500 µg | 20732-500 | More Info |
| CP 24,879 (hydrochloride) | A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… | 1 mg | 10120-1 | More Info |
| CP 24,879 (hydrochloride) | A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… | 10 mg | 10120-10 | More Info |
| CP 24,879 (hydrochloride) | A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… | 5 mg | 10120-5 | More Info |
| CP 24,879 (hydrochloride) | A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… | 50 mg | 10120-50 | More Info |
| CP 31,398 (hydrochloride) | A p53 stabilizing agent; increases active mutant p53 and p53 reporter gene… | 1 mg | 27455-1 | More Info |
| CP 31,398 (hydrochloride) | A p53 stabilizing agent; increases active mutant p53 and p53 reporter gene… | 10 mg | 27455-10 | More Info |
| CP 31,398 (hydrochloride) | A p53 stabilizing agent; increases active mutant p53 and p53 reporter gene… | 5 mg | 27455-5 | More Info |
| CP 809,101 (hydrochloride) | A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… | 10 mg | 33283-10 | More Info |
| CP 809,101 (hydrochloride) | A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… | 25 mg | 33283-25 | More Info |
| CP 809,101 (hydrochloride) | A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… | 5 mg | 33283-5 | More Info |
| CP 809,101 (hydrochloride) | A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… | 50 mg | 33283-50 | More Info |
| CP 93,129 (hydrochloride) | A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… | 1 mg | 34548-1 | More Info |
| CP 93,129 (hydrochloride) | A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… | 10 mg | 34548-10 | More Info |
| CP 93,129 (hydrochloride) | A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… | 25 mg | 34548-25 | More Info |
| CP 93,129 (hydrochloride) | A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… | 5 mg | 34548-5 | More Info |
| CP 94,253 (hydrochloride) | A 5-HT1B agonist (Ki = 2 nM in a radioligand binding assay); selective for… | 10 mg | 29486-10 | More Info |
| CP 94,253 (hydrochloride) | A 5-HT1B agonist (Ki = 2 nM in a radioligand binding assay); selective for… | 25 mg | 29486-25 | More Info |
| CP 94,253 (hydrochloride) | A 5-HT1B agonist (Ki = 2 nM in a radioligand binding assay); selective for… | 5 mg | 29486-5 | More Info |
| CP 945,598 (hydrochloride) | A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… | 1 mg | 11955-1 | More Info |
| CP 945,598 (hydrochloride) | A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… | 10 mg | 11955-10 | More Info |
| CP 945,598 (hydrochloride) | A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… | 25 mg | 11955-25 | More Info |
| CP 945,598 (hydrochloride) | A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… | 5 mg | 11955-5 | More Info |
| CP 99,994 (hydrochloride) | A nonpeptide NK1 receptor antagonist (Ki = 0.25 nM in a radioligand bindin… | 1 mg | 27669-1 | More Info |
| CP 99,994 (hydrochloride) | A nonpeptide NK1 receptor antagonist (Ki = 0.25 nM in a radioligand bindin… | 10 mg | 27669-10 | More Info |
| CP 99,994 (hydrochloride) | A nonpeptide NK1 receptor antagonist (Ki = 0.25 nM in a radioligand bindin… | 5 mg | 27669-5 | More Info |
| 2C-P (hydrochloride) (exempt preparation) | A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… | 1 mg | 15718-1 | More Info |
| C18 Phytoceramide-d3 (t18:0/18:0-d3) | An internal standard for the quantification of C18 phytoceramide by GC- or… | 1 mg | 27199-1 | More Info |
| C22 Phytoceramide-d3 (t18:0/22:0-d3) | An internal standard for the quantification of C22 phytoceramide by GC- or… | 1 mg | 9003465-1 | More Info |
| C22 Phytoceramide-d3 (t18:0/22:0-d3) | An internal standard for the quantification of C22 phytoceramide by GC- or… | 500 µg | 9003465-500 | More Info |
| C16 Phytoceramide (t18:0/16:0) | A phytoceramide; levels increase following heat stress in S. cerevisiae; u… | 5 mg | 22826-5 | More Info |
| C18 Phytoceramide (t18:0/18:0) | A bioactive sphingolipid found in S. cerevisiae, wheat grains, and mammali… | 5 mg | 22686-5 | More Info |
| C2 Phytoceramide (t18:0/2:0) | A bioactive sphingolipid; inhibits formyl peptide-induced oxidant release… | 5 mg | 22823-5 | More Info |
| C22 Phytoceramide (t18:0/22:0) | A sphingolipid; has been found in Moro blood orange (C. sinensis) peels an… | 1 mg | 9003464-1 | More Info |
| C22 Phytoceramide (t18:0/22:0) | A sphingolipid; has been found in Moro blood orange (C. sinensis) peels an… | 5 mg | 9003464-5 | More Info |
| C24 Phytoceramide (t18:0/24:0) | A sphingolipid and phytoceramide; used with other ceramides to create stra… | 1 mg | 22827-1 | More Info |
| C24 Phytoceramide (t18:0/24:0) | A sphingolipid and phytoceramide; used with other ceramides to create stra… | 5 mg | 22827-5 | More Info |
| C6 Phytoceramide (t18:0/6:0) | A bioactive sphingolipid and cell-permeable analog of phytoceramide; induc… | 5 mg | 24438-5 | More Info |
| C8 Phytoceramide (t18:0/8:0) | A sphingolipid; a cell-permeable analog of phytosphingosine | 5 mg | 24357-5 | More Info |
| CPI-1189 | A benzamide; inhibits phosphorylation of p38 MAPK in IL-1β-stimulated… | 100 mg | 29187-100 | More Info |
| CPI-1189 | A benzamide; inhibits phosphorylation of p38 MAPK in IL-1β-stimulated… | 25 mg | 29187-25 | More Info |
| CPI-1189 | A benzamide; inhibits phosphorylation of p38 MAPK in IL-1β-stimulated… | 250 mg | 29187-250 | More Info |
| CPI-1189 | A benzamide; inhibits phosphorylation of p38 MAPK in IL-1β-stimulated… | 50 mg | 29187-50 | More Info |
| CPI-169 | A selective EZH2 inhibitor (IC50s = 0.24, 0.51, and 6.1 nM for wild-type E… | 1 mg | 18299-1 | More Info |
| CPI-169 | A selective EZH2 inhibitor (IC50s = 0.24, 0.51, and 6.1 nM for wild-type E… | 5 mg | 18299-5 | 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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