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.
Selective HDAC4 and HDAC5 inhibitor.
Alkaloid compound originally found in Corydalis...
Valsartan impurity
DP1 antagonist.
ROCK inhibitor.
Amino acid precursor of dopamine.
FAK inhibitor.
Ergot derivative found in Claviceps; α1-adrene...
B-Raf and c-Raf inhibitor.
Somatostatin analog, peptide; somatostatin agon...
Bisphosphonate; FPPS inhibitor.
Endogenous amino acid, forms disulfide bridges ...
Endogenous sugar produced from glucose, require...
Indoleamine 2,3-dioxygenase inhibitor.
Iron chelator.
FIASMA, μOR agonist, potential HCN channel blo...
Walrycin response regulator inhibitor.
β-lactam cephalosporin; penicillin binding pro...
Triterpene aglycone originally found in Centell...
Fermentation impurity