CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 1 of 1
Non-Antibody Products
Page 1,064 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Rosuvastatin lactone | The lactone form of rosuvastatin; an inhibitor of CYP2C9.1 and CYP2C9.3 (I… | 50 mg | 33885-50 | More Info |
| Rotenone | An inhibitor of mitochondrial complex I; inhibits NADH / DB oxidoreductase… | 100 mg | 13995-100 | More Info |
| Rotenone | An inhibitor of mitochondrial complex I; inhibits NADH / DB oxidoreductase… | 25 mg | 13995-25 | More Info |
| Rotenone | An inhibitor of mitochondrial complex I; inhibits NADH / DB oxidoreductase… | 50 mg | 13995-50 | More Info |
| Rotigotine | A non-selective dopamine receptor agonist (pEC50s = 9.6, 10.4, 8.2, 7.7, a… | 5 mg | 20246-5 | More Info |
| Rotigotine | A non-selective dopamine receptor agonist (pEC50s = 9.6, 10.4, 8.2, 7.7, a… | 1 mg | 20246-1 | More Info |
| Rotigotine | A non-selective dopamine receptor agonist (pEC50s = 9.6, 10.4, 8.2, 7.7, a… | 10 mg | 20246-10 | More Info |
| Rotigotine | A non-selective dopamine receptor agonist (pEC50s = 9.6, 10.4, 8.2, 7.7, a… | 25 mg | 20246-25 | More Info |
| Rottlerin | Inhibits PKCδ (IC50 = 3 µM), CAM kinase III, and a wide range… | 10 mg | 12006-10 | More Info |
| Rottlerin | Inhibits PKCδ (IC50 = 3 µM), CAM kinase III, and a wide range… | 50 mg | 12006-50 | More Info |
| Roxadustat | An analog of 2-OG that has been developed as an inhibitor of HIF-PHs | 10 mg | 15294-10 | More Info |
| Roxadustat | An analog of 2-OG that has been developed as an inhibitor of HIF-PHs | 25 mg | 15294-25 | More Info |
| Roxadustat | An analog of 2-OG that has been developed as an inhibitor of HIF-PHs | 5 mg | 15294-5 | More Info |
| Roxadustat | An analog of 2-OG that has been developed as an inhibitor of HIF-PHs | 50 mg | 15294-50 | More Info |
| Roxadustat-d5 | An internal standard for the quantification of roxadustat by GC- or LC-MS | 1 mg | 34235-1 | More Info |
| Roxatidine | A histamine H2 receptor antagonist and major active metabolite of roxatidi… | 1 mg | 36111-1 | More Info |
| Roxatidine | A histamine H2 receptor antagonist and major active metabolite of roxatidi… | 10 mg | 36111-10 | More Info |
| Roxatidine | A histamine H2 receptor antagonist and major active metabolite of roxatidi… | 5 mg | 36111-5 | More Info |
| Roxatidine | A histamine H2 receptor antagonist and major active metabolite of roxatidi… | 500 µg | 36111-500 | More Info |
| Roxatidine Acetate (hydrochloride) | A competitive histamine H2 receptor antagonist upon conversion to its acti… | 1 g | 21248-1 | More Info |
| Roxatidine Acetate (hydrochloride) | A competitive histamine H2 receptor antagonist upon conversion to its acti… | 250 mg | 21248-250 | More Info |
| Roxatidine Acetate (hydrochloride) | A competitive histamine H2 receptor antagonist upon conversion to its acti… | 5 g | 21248-5 | More Info |
| Roxatidine Acetate (hydrochloride) | A competitive histamine H2 receptor antagonist upon conversion to its acti… | 500 mg | 21248-500 | More Info |
| Roxatidine-d10 (hemioxalate) | An internal standard for the quantification of roxatidine by GC- or LC-MS | 1 mg | 34007-1 | More Info |
| Roxatidine-d10 (hemioxalate) | An internal standard for the quantification of roxatidine by GC- or LC-MS | 5 mg | 34007-5 | More Info |
| Roxithromycin | A macrolide antibiotic; active against five strains each of Staphylococcus… | 1 g | 19465-1 | More Info |
| Roxithromycin | A macrolide antibiotic; active against five strains each of Staphylococcus… | 10 g | 19465-10 | More Info |
| Roxithromycin | A macrolide antibiotic; active against five strains each of Staphylococcus… | 5 g | 19465-5 | More Info |
| (R)-3-Oxo-cyclopentaneacetic acid methyl ester | A synthetic intermediate useful for pharmaceutical synthesis. | 50 mg | 11415-50 | More Info |
| (R)-3-Oxo-cyclopentanecarboxylic acid methyl ester | A synthetic intermediate useful for pharmaceutical synthesis. | 50 mg | 11416-50 | More Info |
| RP 70676 | An inhibitor of ACAT (IC50 = 44 nM for the rabbit enzyme); reduces plasma… | 100 mg | 39529-100 | More Info |
| RP 70676 | An inhibitor of ACAT (IC50 = 44 nM for the rabbit enzyme); reduces plasma… | 25 mg | 39529-25 | More Info |
| RP 70676 | An inhibitor of ACAT (IC50 = 44 nM for the rabbit enzyme); reduces plasma… | 50 mg | 39529-50 | More Info |
| Rp-Adenosine-5'-O-(1-thiodiphosphate) (sodium salt) | An isomer of ADP-α-S; inhibitor of phosphorylase kinase (Ki = 0.53 &… | 2.2 mg | 38533-22 | More Info |
| Rp-Adenosine-5'-O-(1-thiotriphosphate) (sodium salt) | An isomer of ATP-α-S and a P2Y1 receptor agonist; increases calcium… | 2.6 mg | 38535-26 | More Info |
| 10(R)-PAHSA | A stereoisomer of 10-PAHSA | 1 mg | 21362-1 | More Info |
| 10(R)-PAHSA | A stereoisomer of 10-PAHSA | 500 µg | 21362-500 | More Info |
| 9(R)-PAHSA | A stereoisomer of 9-PAHSA; the predominant form of 9-PAHSA that accumulate… | 1 mg | 18022-1 | More Info |
| 9(R)-PAHSA | A stereoisomer of 9-PAHSA; the predominant form of 9-PAHSA that accumulate… | 500 µg | 18022-500 | More Info |
| R-Palmitoyl-(1-methyl) Ethanolamide | A synthetic analog of PEA which incorporates an (R)-methyl group vicinal t… | 10 mg | 90353-10 | More Info |
| R-Palmitoyl-(1-methyl) Ethanolamide | A synthetic analog of PEA which incorporates an (R)-methyl group vicinal t… | 5 mg | 90353-5 | More Info |
| R-Palmitoyl-(1-methyl) Ethanolamide | A synthetic analog of PEA which incorporates an (R)-methyl group vicinal t… | 50 mg | 90353-50 | More Info |
| R-Palmitoyl-(2-methyl) Ethanolamide | A metabolically stable analog of the anti-inflammatory endogenous CB, PEA;… | 10 mg | 90357-10 | More Info |
| R-Palmitoyl-(2-methyl) Ethanolamide | A metabolically stable analog of the anti-inflammatory endogenous CB, PEA;… | 5 mg | 90357-5 | More Info |
| R-Palmitoyl-(2-methyl) Ethanolamide | A metabolically stable analog of the anti-inflammatory endogenous CB, PEA;… | 50 mg | 90357-50 | More Info |
| Rp-8-bromo-Cyclic AMPS (sodium salt) | A membrane-permeable antagonist of cAMP-dependent PKAs; resistant to hydro… | 1 mg | 21584-1 | More Info |
| Rp-8-bromo-Cyclic AMPS (sodium salt) | A membrane-permeable antagonist of cAMP-dependent PKAs; resistant to hydro… | 5 mg | 21584-5 | More Info |
| Rp-8-bromo-Cyclic AMPS (sodium salt) | A membrane-permeable antagonist of cAMP-dependent PKAs; resistant to hydro… | 500 µg | 21584-500 | More Info |
| Rp-8-bromo-Cyclic GMPS (sodium salt) | A cell-permeable cGMP analog that binds cGK without activating it, resulti… | 1 mg | 18441-1 | More Info |
| Rp-8-bromo-Cyclic GMPS (sodium salt) | A cell-permeable cGMP analog that binds cGK without activating it, resulti… | 5 mg | 18441-5 | 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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