CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 526 of 865
Non-Antibody Products
Page 526 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| MPP+ Iodide | An active metabolite of MPTP, a neurotoxin used to cause selective destruc… | 250 mg | 16958-250 | More Info |
| MPP+ Iodide | An active metabolite of MPTP, a neurotoxin used to cause selective destruc… | 50 mg | 16958-50 | More Info |
| MPP-PICA | An analytical reference standard that is structurally similar to known syn… | 1 mg | 31268-1 | More Info |
| MPP-PICA | An analytical reference standard that is structurally similar to known syn… | 5 mg | 31268-5 | More Info |
| Mpro Inhibitor 11b | An inhibitor of Mpro (IC50 = 0.04 µM in a TR-FRET assay); reduces vi… | 1 mg | 31345-1 | More Info |
| Mpro Inhibitor 11b | An inhibitor of Mpro (IC50 = 0.04 µM in a TR-FRET assay); reduces vi… | 10 mg | 31345-10 | More Info |
| Mpro Inhibitor 11b | An inhibitor of Mpro (IC50 = 0.04 µM in a TR-FRET assay); reduces vi… | 5 mg | 31345-5 | More Info |
| Mps1-IN-1 | A selective inhibitor of Mps1 kinase (IC50 = 367 nM); disrupts the recruit… | 1 mg | 19175-1 | More Info |
| Mps1-IN-1 | A selective inhibitor of Mps1 kinase (IC50 = 367 nM); disrupts the recruit… | 10 mg | 19175-10 | More Info |
| Mps1-IN-1 | A selective inhibitor of Mps1 kinase (IC50 = 367 nM); disrupts the recruit… | 5 mg | 19175-5 | More Info |
| Mps1-IN-1 | A selective inhibitor of Mps1 kinase (IC50 = 367 nM); disrupts the recruit… | 500 µg | 19175-500 | More Info |
| Mps1-IN-2 | An inhibitor of Mps1 (IC50 = 145 nM); 1,000-fold selective for Mps1 over a… | 1 mg | 19401-1 | More Info |
| Mps1-IN-2 | An inhibitor of Mps1 (IC50 = 145 nM); 1,000-fold selective for Mps1 over a… | 10 mg | 19401-10 | More Info |
| Mps1-IN-2 | An inhibitor of Mps1 (IC50 = 145 nM); 1,000-fold selective for Mps1 over a… | 25 mg | 19401-25 | More Info |
| Mps1-IN-2 | An inhibitor of Mps1 (IC50 = 145 nM); 1,000-fold selective for Mps1 over a… | 5 mg | 19401-5 | More Info |
| Mps1/TTK Inhibitor | An inhibitor of Mps1 / TTK (IC50 = 5.8 nM); inhibits Mps1 phosphorylation… | 1 mg | 25554-1 | More Info |
| Mps1/TTK Inhibitor | An inhibitor of Mps1 / TTK (IC50 = 5.8 nM); inhibits Mps1 phosphorylation… | 10 mg | 25554-10 | More Info |
| Mps1/TTK Inhibitor | An inhibitor of Mps1 / TTK (IC50 = 5.8 nM); inhibits Mps1 phosphorylation… | 25 mg | 25554-25 | More Info |
| Mps1/TTK Inhibitor | An inhibitor of Mps1 / TTK (IC50 = 5.8 nM); inhibits Mps1 phosphorylation… | 5 mg | 25554-5 | More Info |
| MPT0B014 | A tubulin polymerization inhibitor; inhibits proliferation of A549, H1299,… | 1 mg | 21718-1 | More Info |
| MPT0B014 | A tubulin polymerization inhibitor; inhibits proliferation of A549, H1299,… | 10 mg | 21718-10 | More Info |
| MPT0B014 | A tubulin polymerization inhibitor; inhibits proliferation of A549, H1299,… | 25 mg | 21718-25 | More Info |
| MPT0B014 | A tubulin polymerization inhibitor; inhibits proliferation of A549, H1299,… | 5 mg | 21718-5 | More Info |
| MR2938 | An AChE inhibitor (IC50 = 5.04 µM); selective for AChE over BChE (IC… | 1 mg | 39035-1 | More Info |
| MR2938 | An AChE inhibitor (IC50 = 5.04 µM); selective for AChE over BChE (IC… | 10 mg | 39035-10 | More Info |
| MR2938 | An AChE inhibitor (IC50 = 5.04 µM); selective for AChE over BChE (IC… | 5 mg | 39035-5 | More Info |
| MR1/β2-Microglobulin Complex (human, recombinant) | Source: Recombinant human MR1 and β2-microglobulin expressed in E. co… | 20 µg | 30585-20 | More Info |
| MRE-269 | A stable analogue of prostacyclin that potently and selectively activates… | 1 mg | 10010412-1 | More Info |
| MRE-269 | A stable analogue of prostacyclin that potently and selectively activates… | 10 mg | 10010412-10 | More Info |
| MRE-269 | A stable analogue of prostacyclin that potently and selectively activates… | 5 mg | 10010412-5 | More Info |
| MRE-269 | A stable analogue of prostacyclin that potently and selectively activates… | 50 mg | 10010412-50 | More Info |
| MreB Perturbing Compound A22 | A benzylisothiourea compound that interacts with the ATP binding site of M… | 10 mg | 15870-10 | More Info |
| MreB Perturbing Compound A22 | A benzylisothiourea compound that interacts with the ATP binding site of M… | 25 mg | 15870-25 | More Info |
| MreB Perturbing Compound A22 | A benzylisothiourea compound that interacts with the ATP binding site of M… | 50 mg | 15870-50 | More Info |
| MR1 Immunoaffinity Sorbent | Consists of Cayman's MR1 monoclonal antibody coupled to CNBr-activated Sep… | 400 µL | 38215-400 | More Info |
| MRK-016 | An inverse agonist of α5 subunit-containing GABAA receptors; selecti… | 1 mg | 36656-1 | More Info |
| MRK-016 | An inverse agonist of α5 subunit-containing GABAA receptors; selecti… | 10 mg | 36656-10 | More Info |
| MRK-016 | An inverse agonist of α5 subunit-containing GABAA receptors; selecti… | 25 mg | 36656-25 | More Info |
| MRK-016 | An inverse agonist of α5 subunit-containing GABAA receptors; selecti… | 5 mg | 36656-5 | More Info |
| MRK-560 | A potent inhibitor of γ-secretase (IC50 = 0.65 nM); reduces diethano… | 1 mg | 27599-1 | More Info |
| MRK-560 | A potent inhibitor of γ-secretase (IC50 = 0.65 nM); reduces diethano… | 5 mg | 27599-5 | More Info |
| MRS1523 | An adenosine A3 receptor antagonist; binds to the human adenosine A3 recep… | 1 mg | 17128-1 | More Info |
| MRS1523 | An adenosine A3 receptor antagonist; binds to the human adenosine A3 recep… | 10 mg | 17128-10 | More Info |
| MRS1523 | An adenosine A3 receptor antagonist; binds to the human adenosine A3 recep… | 25 mg | 17128-25 | More Info |
| MRS1523 | An adenosine A3 receptor antagonist; binds to the human adenosine A3 recep… | 5 mg | 17128-5 | More Info |
| MRS1706 | A selective adenosine A2B receptor inverse agonist (Ki = 1.39 nM) | 1 mg | 17417-1 | More Info |
| MRS1706 | A selective adenosine A2B receptor inverse agonist (Ki = 1.39 nM) | 10 mg | 17417-10 | More Info |
| MRS1706 | A selective adenosine A2B receptor inverse agonist (Ki = 1.39 nM) | 5 mg | 17417-5 | More Info |
| MRS1706 | A selective adenosine A2B receptor inverse agonist (Ki = 1.39 nM) | 50 mg | 17417-50 | More Info |
| MRS1754 | An adenosine A2B receptor antagonist (Ki = 1.97 nM); selective for adenosi… | 10 mg | 33501-10 | More Info |
| MRS1754 | An adenosine A2B receptor antagonist (Ki = 1.97 nM); selective for adenosi… | 25 mg | 33501-25 | More Info |
| MRS1754 | An adenosine A2B receptor antagonist (Ki = 1.97 nM); selective for adenosi… | 5 mg | 33501-5 | More Info |
| MRS1754 | An adenosine A2B receptor antagonist (Ki = 1.97 nM); selective for adenosi… | 50 mg | 33501-50 | More Info |
| MRS1845 | An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… | 1 mg | 36814-1 | More Info |
| MRS1845 | An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… | 10 mg | 36814-10 | More Info |
| MRS1845 | An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… | 5 mg | 36814-5 | More Info |
| MRS1845 | An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… | 500 µg | 36814-500 | More Info |
| MRS2578 | A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… | 10 mg | 19704-10 | More Info |
| MRS2578 | A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… | 25 mg | 19704-25 | More Info |
| MRS2578 | A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… | 5 mg | 19704-5 | More Info |
| MRS2578 | A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… | 50 mg | 19704-50 | More Info |
| MRS2179 (ammonium salt hydrate) | A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… | 1 mg | 10011450-1 | More Info |
| MRS2179 (ammonium salt hydrate) | A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… | 10 mg | 10011450-10 | More Info |
| MRS2179 (ammonium salt hydrate) | A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… | 5 mg | 10011450-5 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 1 mg | 22138-1 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 10 mg | 22138-10 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 25 mg | 22138-25 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 5 mg | 22138-5 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 1 mg | 19905-1 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 10 mg | 19905-10 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 25 mg | 19905-25 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 5 mg | 19905-5 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 1 mg | 19916-1 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 10 mg | 19916-10 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 25 mg | 19916-25 | 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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