Mouse RAR-related Orphan Receptor, Gamma Reporter Assay System |
mRORγ Reporter Cells are prepared using INDIGO's proprietary CryoMit… |
96 Well |
21401-96 |
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Mouse/Rat Peroxisome Proliferator-Activated Receptor Gamma Reporter Assay System |
mrPPARγ Reporter Cells are prepared using INDIGO's proprietary CryoM… |
3x32 Well |
15761-332 |
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Mouse/Rat Peroxisome Proliferator-Activated Receptor Gamma Reporter Assay System |
mrPPARγ Reporter Cells are prepared using INDIGO's proprietary CryoM… |
96 Well |
15761-96 |
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|
Moxalactam (sodium salt) |
A β-lactam antibiotic in the cephalosporin class |
1 g |
15869-1 |
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Moxalactam (sodium salt) |
A β-lactam antibiotic in the cephalosporin class |
250 mg |
15869-250 |
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Moxalactam (sodium salt) |
A β-lactam antibiotic in the cephalosporin class |
500 mg |
15869-500 |
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Moxidectin |
A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… |
10 mg |
17165-10 |
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Moxidectin |
A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… |
25 mg |
17165-25 |
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Moxidectin |
A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… |
5 mg |
17165-5 |
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Moxidectin |
A macrocyclic lactone endectocide and a derivative of nemadectin; reduces… |
50 mg |
17165-50 |
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|
Moxidectin-d3 |
An internal standard for the quantification of moxidectin by GC- or LC-MS |
1 mg |
28766-1 |
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Moxifloxacin-d4 (hydrochloride) |
An internal standard for the quantification of moxifloxacin by GC- or LC-M… |
1 mg |
22564-1 |
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Moxifloxacin-d4 (hydrochloride) |
An internal standard for the quantification of moxifloxacin by GC- or LC-M… |
500 µg |
22564-500 |
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|
Moxifloxacin (hydrochloride) |
A fluoroquinolone antibiotic; active against 390 clinical isolates of vari… |
1 g |
14830-1 |
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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 |
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Moxifloxacin N-Sulfate (sodium salt) |
A metabolite of moxifloxacin |
10 mg |
26621-10 |
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|
Moxifloxacin N-Sulfate (sodium salt) |
A metabolite of moxifloxacin |
5 mg |
26621-5 |
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Moxonidine |
An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… |
10 mg |
25639-10 |
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Moxonidine |
An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… |
100 mg |
25639-100 |
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Moxonidine |
An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… |
250 mg |
25639-250 |
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Moxonidine |
An imidazoline I1 and α2A-AR agonist (Kis = 56 and 150 nM, respectiv… |
50 mg |
25639-50 |
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Mozavaptan-d6 |
An internal standard for the quantification of mozavaptan by GC- or LC-MS |
1 mg |
31321-1 |
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Mozavaptan-d6 |
An internal standard for the quantification of mozavaptan by GC- or LC-MS |
500 µg |
31321-500 |
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Mozavaptan (hydrochloride) |
A vasopressin V2 receptor antagonist (Ki = 9.42 nM in HeLa cells expressin… |
10 mg |
16664-10 |
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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
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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 |
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MOZ-IN-2 |
An inhibitor of KAT6A / MOZ (IC50 = 125 µM) |
10 mg |
27686-10 |
More Info
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MOZ-IN-2 |
An inhibitor of KAT6A / MOZ (IC50 = 125 µM) |
25 mg |
27686-25 |
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MOZ-IN-2 |
An inhibitor of KAT6A / MOZ (IC50 = 125 µM) |
5 mg |
27686-5 |
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MOZ-IN-3 |
An inhibitor of KAT6A and KAT6B (IC50s = 8 and 28 nM, respectively); selec… |
1 mg |
27402-1 |
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MOZ-IN-3 |
An inhibitor of KAT6A and KAT6B (IC50s = 8 and 28 nM, respectively); selec… |
5 mg |
27402-5 |
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MOZ-IN-3 |
An inhibitor of KAT6A and KAT6B (IC50s = 8 and 28 nM, respectively); selec… |
500 µg |
27402-500 |
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MP-A08 |
An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… |
1 mg |
21903-1 |
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MP-A08 |
An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… |
10 mg |
21903-10 |
More Info
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MP-A08 |
An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… |
25 mg |
21903-25 |
More Info
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MP-A08 |
An inhibitor of SPHK1 and SPHK2 (Kis = 27 and 6.9 µM, respectively);… |
5 mg |
21903-5 |
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MPC-3100 |
An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… |
1 mg |
22496-1 |
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MPC-3100 |
An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… |
10 mg |
22496-10 |
More Info
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MPC-3100 |
An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… |
25 mg |
22496-25 |
More Info
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MPC-3100 |
An inhibitor of Hsp90 (IC50 = 0.14 µM); inhibits proliferation of a… |
5 mg |
22496-5 |
More Info
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MPC-6827 (hydrochloride) |
An inhibitor of tubulin polymerization with anticancer activity; inhibits… |
1 mg |
32872-1 |
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MPC-6827 (hydrochloride) |
An inhibitor of tubulin polymerization with anticancer activity; inhibits… |
10 mg |
32872-10 |
More Info
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MPC-6827 (hydrochloride) |
An inhibitor of tubulin polymerization with anticancer activity; inhibits… |
5 mg |
32872-5 |
More Info
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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
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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
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