CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 525 of 865
Non-Antibody Products
Page 525 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Mouse RAR-related Orphan Receptor, Gamma Reporter Assay System | mRORγ Reporter Cells are prepared using INDIGO's proprietary CryoMit… | 96 Well | 21401-96 | More Info |
| Mouse/Rat Peroxisome Proliferator-Activated Receptor Gamma Reporter Assay System | mrPPARγ Reporter Cells are prepared using INDIGO's proprietary CryoM… | 3x32 Well | 15761-332 | More Info |
| Mouse/Rat Peroxisome Proliferator-Activated Receptor Gamma Reporter Assay System | mrPPARγ Reporter Cells are prepared using INDIGO's proprietary CryoM… | 96 Well | 15761-96 | More Info |
| Moxalactam (sodium salt) | A β-lactam antibiotic in the cephalosporin class | 1 g | 15869-1 | More Info |
| Moxalactam (sodium salt) | A β-lactam antibiotic in the cephalosporin class | 250 mg | 15869-250 | More Info |
| Moxalactam (sodium salt) | A β-lactam antibiotic in the cephalosporin class | 500 mg | 15869-500 | More Info |
| Moxidectin | A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… | 10 mg | 17165-10 | More Info |
| Moxidectin | A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… | 25 mg | 17165-25 | More Info |
| Moxidectin | A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… | 5 mg | 17165-5 | More Info |
| Moxidectin | A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… | 50 mg | 17165-50 | More Info |
| Moxidectin-d3 | An internal standard for the quantification of moxidectin by GC- or LC-MS | 1 mg | 28766-1 | More Info |
| Moxifloxacin-d4 (hydrochloride) | An internal standard for the quantification of moxifloxacin by GC- or LC-M… | 1 mg | 22564-1 | More Info |
| Moxifloxacin-d4 (hydrochloride) | An internal standard for the quantification of moxifloxacin by GC- or LC-M… | 500 µg | 22564-500 | More Info |
| Moxifloxacin (hydrochloride) | A fluoroquinolone antibiotic; active against 390 clinical isolates of vari… | 1 g | 14830-1 | More Info |
| Moxifloxacin (hydrochloride) | A fluoroquinolone antibiotic; active against 390 clinical isolates of vari… | 100 mg | 14830-100 | More Info |
| Moxifloxacin (hydrochloride) | A fluoroquinolone antibiotic; active against 390 clinical isolates of vari… | 50 mg | 14830-50 | More Info |
| Moxifloxacin (hydrochloride) | A fluoroquinolone antibiotic; active against 390 clinical isolates of vari… | 500 mg | 14830-500 | More Info |
| Moxifloxacin N-Sulfate (sodium salt) | A metabolite of moxifloxacin | 1 mg | 26621-1 | More Info |
| Moxifloxacin N-Sulfate (sodium salt) | A metabolite of moxifloxacin | 10 mg | 26621-10 | More Info |
| Moxifloxacin N-Sulfate (sodium salt) | A metabolite of moxifloxacin | 5 mg | 26621-5 | More Info |
| Moxonidine | An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… | 10 mg | 25639-10 | More Info |
| Moxonidine | An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… | 100 mg | 25639-100 | More Info |
| Moxonidine | An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… | 250 mg | 25639-250 | More Info |
| Moxonidine | An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… | 50 mg | 25639-50 | More Info |
| Mozavaptan-d6 | An internal standard for the quantification of mozavaptan by GC- or LC-MS | 1 mg | 31321-1 | More Info |
| Mozavaptan-d6 | An internal standard for the quantification of mozavaptan by GC- or LC-MS | 500 µg | 31321-500 | More Info |
| Mozavaptan (hydrochloride) | A vasopressin V2 receptor antagonist (Ki = 9.42 nM in HeLa cells expressin… | 10 mg | 16664-10 | More Info |
| Mozavaptan (hydrochloride) | A vasopressin V2 receptor antagonist (Ki = 9.42 nM in HeLa cells expressin… | 100 mg | 16664-100 | More Info |
| Mozavaptan (hydrochloride) | A vasopressin V2 receptor antagonist (Ki = 9.42 nM in HeLa cells expressin… | 5 mg | 16664-5 | More Info |
| Mozavaptan (hydrochloride) | A vasopressin V2 receptor antagonist (Ki = 9.42 nM in HeLa cells expressin… | 50 mg | 16664-50 | More Info |
| MOZ-IN-2 | An inhibitor of KAT6A / MOZ (IC50 = 125 µM) | 1 mg | 27686-1 | More Info |
| MOZ-IN-2 | An inhibitor of KAT6A / MOZ (IC50 = 125 µM) | 10 mg | 27686-10 | More Info |
| MOZ-IN-2 | An inhibitor of KAT6A / MOZ (IC50 = 125 µM) | 25 mg | 27686-25 | More Info |
| MOZ-IN-2 | An inhibitor of KAT6A / MOZ (IC50 = 125 µM) | 5 mg | 27686-5 | More Info |
| MOZ-IN-3 | An inhibitor of KAT6A and KAT6B (IC50s = 8 and 28 nM, respectively); selec… | 1 mg | 27402-1 | More Info |
| MOZ-IN-3 | An inhibitor of KAT6A and KAT6B (IC50s = 8 and 28 nM, respectively); selec… | 5 mg | 27402-5 | More Info |
| MOZ-IN-3 | An inhibitor of KAT6A and KAT6B (IC50s = 8 and 28 nM, respectively); selec… | 500 µg | 27402-500 | More Info |
| MP-A08 | An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… | 1 mg | 21903-1 | More Info |
| MP-A08 | An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… | 10 mg | 21903-10 | More Info |
| MP-A08 | An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… | 25 mg | 21903-25 | More Info |
| MP-A08 | An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… | 5 mg | 21903-5 | More Info |
| MPC-3100 | An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… | 1 mg | 22496-1 | More Info |
| MPC-3100 | An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… | 10 mg | 22496-10 | More Info |
| MPC-3100 | An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… | 25 mg | 22496-25 | More Info |
| MPC-3100 | An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… | 5 mg | 22496-5 | More Info |
| MPC-6827 (hydrochloride) | An inhibitor of tubulin polymerization with anticancer activity; inhibits… | 1 mg | 32872-1 | More Info |
| MPC-6827 (hydrochloride) | An inhibitor of tubulin polymerization with anticancer activity; inhibits… | 10 mg | 32872-10 | More Info |
| MPC-6827 (hydrochloride) | An inhibitor of tubulin polymerization with anticancer activity; inhibits… | 5 mg | 32872-5 | More Info |
| 8-M-PDOT | An MT2 receptor agonist (Ki = 1.12 nM); is 5.2-fold selective for MT2 over… | 10 mg | 29521-10 | More Info |
| 8-M-PDOT | An MT2 receptor agonist (Ki = 1.12 nM); is 5.2-fold selective for MT2 over… | 25 mg | 29521-25 | More Info |
| 8-M-PDOT | An MT2 receptor agonist (Ki = 1.12 nM); is 5.2-fold selective for MT2 over… | 5 mg | 29521-5 | More Info |
| 8-M-PDOT | An MT2 receptor agonist (Ki = 1.12 nM); is 5.2-fold selective for MT2 over… | 50 mg | 29521-50 | More Info |
| MPEG(30000)-NHS ester | A PEGylated and esterified form of NHS | 1 g | 39743-1 | More Info |
| MPEG(30000)-NHS ester | A PEGylated and esterified form of NHS | 250 mg | 39743-250 | More Info |
| MPEG(30000)-NHS ester | A PEGylated and esterified form of NHS | 500 mg | 39743-500 | More Info |
| MPEP (hydrochloride) | A potent, highly selective, and centrally active antagonist at the mGlu5a… | 10 mg | 14536-10 | More Info |
| MPEP (hydrochloride) | A potent, highly selective, and centrally active antagonist at the mGlu5a… | 25 mg | 14536-25 | More Info |
| MPEP (hydrochloride) | A potent, highly selective, and centrally active antagonist at the mGlu5a… | 5 mg | 14536-5 | More Info |
| MPEP (hydrochloride) | A potent, highly selective, and centrally active antagonist at the mGlu5a… | 50 mg | 14536-50 | More Info |
| M2 Peptide | An M2 TAM-targeting peptide; has been used in the generation of anticancer… | 1 mg | 40263-1 | More Info |
| MPI-0441138 | A potent inducer of apoptosis and growth inhibitor (EC50 = 2 nM for both p… | 1 mg | 13098-1 | More Info |
| MPI-0441138 | A potent inducer of apoptosis and growth inhibitor (EC50 = 2 nM for both p… | 10 mg | 13098-10 | More Info |
| MPI-0441138 | A potent inducer of apoptosis and growth inhibitor (EC50 = 2 nM for both p… | 25 mg | 13098-25 | More Info |
| MPI-0441138 | A potent inducer of apoptosis and growth inhibitor (EC50 = 2 nM for both p… | 5 mg | 13098-5 | More Info |
| MPI-0479605 | A potent inhibitor of MPS1 (IC50 = 1.8 nM); selective for MPS1 over a pane… | 1 mg | 22136-1 | More Info |
| MPI-0479605 | A potent inhibitor of MPS1 (IC50 = 1.8 nM); selective for MPS1 over a pane… | 10 mg | 22136-10 | More Info |
| MPI-0479605 | A potent inhibitor of MPS1 (IC50 = 1.8 nM); selective for MPS1 over a pane… | 25 mg | 22136-25 | More Info |
| MPI-0479605 | A potent inhibitor of MPS1 (IC50 = 1.8 nM); selective for MPS1 over a pane… | 5 mg | 22136-5 | More Info |
| MPO-IN-28 | An adenosine A2B receptor antagonist (Ki = 2.15 µM in HEK293 cells e… | 1 mg | 37192-1 | More Info |
| MPO-IN-28 | An adenosine A2B receptor antagonist (Ki = 2.15 µM in HEK293 cells e… | 10 mg | 37192-10 | More Info |
| MPO-IN-28 | An adenosine A2B receptor antagonist (Ki = 2.15 µM in HEK293 cells e… | 25 mg | 37192-25 | More Info |
| MPO-IN-28 | An adenosine A2B receptor antagonist (Ki = 2.15 µM in HEK293 cells e… | 5 mg | 37192-5 | More Info |
| MPP-BUTINACA | An analytical reference standard that is structurally similar to known syn… | 1 mg | 36852-1 | More Info |
| MPP-BUTINACA | An analytical reference standard that is structurally similar to known syn… | 5 mg | 36852-5 | More Info |
| MPP+ Iodide | An active metabolite of MPTP, a neurotoxin used to cause selective destruc… | 100 mg | 16958-100 | 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
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