Description
AGI-6780 is an inhibitor of isocitrate dehydrogenase (IDH) that displays anticancer activity. This compound induces differentiation in acute myeloid leukemia (AML) and TF-1 erythroleukemia cells.
| Product Unit Size | Cost | Quantity | Stock |
|---|
AGI-6780 is an inhibitor of isocitrate dehydrogenase (IDH) that displays anticancer activity. This compound induces differentiation in acute myeloid leukemia (AML) and TF-1 erythroleukemia cells.
| Cas No. | 1432660-47-3 |
|---|---|
| Purity | ≥98% |
| Formula | C21H18F3N3O3S2 |
| Formula Wt. | 481.51 |
| IUPAC Name | N-Cyclopropyl-4-(3-thienyl)-3-({[3-(trifluoromethyl)phenyl]carbamoyl}amino)benzenesulfonamide |
| Synonym | AGI 6780, AGI6780 |
| Solubility | DMSO 96 mg/mL (199.37 mM) Ethanol 96 mg/mL (199.37 mM) Water Insoluble |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Lee WY, Chen KC, Chen HY, et al. Potential mitochondrial isocitrate dehydrogenase R140Q mutant inhibitor from traditional Chinese medicine against cancers. Biomed Res Int. 2014;2014:364625. PMID: 24995286.
Wang F, Travins J, DeLaBarre B, et al. Targeted inhibition of mutant IDH2 in leukemia cells induces cellular differentiation. Science. 2013 May 3;340(6132):622-6. PMID: 23558173.
Peptide, HIV-1 RT A2.1 epitope.
Estradiol metabolite.
Imidzoline derivative; MDM2 inhibitor.
Polypeptide; peptidoglycan inhibitor.
Potential ATP-sensitive K+ channel blocker, pot...
NSAID; TRPA1 agonist, COX-2 inhibitor.
Xanthine derivative; adenosine antagonist, PDE ...
ITC, radical scavenger.
5-Fluorouracil prodrug, pyrimidine nucleoside a...
CB2 receptor antagonist.
Alkaloid originally found in species of Nicotia...
Dipeptide.
Promotes Aβ clearance.
Used to study embryonic cloning; microtubule po...
CDK1/2 inhibitor.
VEGF-C/Nrp2 inhibitor. Leukotriene receptor ant...
Voltage-gated K+ channel blocker.
Tetracycline; protein translation inhibitor, MM...
Diterpenoid epoxide found in Tripterygium.
Peptide, inactive mastoparan analog used to mea...