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.
Wnt/beta-catenin/CBP inhibitor
Steroid; glucocorticoid agonist.
Caffeic acid ester found in Melissa, Salvia, an...
Endogenous purine nucleotide base, required for...
Imidazole; 14-α demethylase inhibitor.
Polyphenol found in Camilla sinensis; HIV integ...
Endogenous opioid peptide; μOR agonist.
Cdc42 inhibitor.
Bioactive compound from olive tree.
Endogenous opioid peptide derived from the β-c...
Synthetic quinone CoQ analog, promotes mitochon...
L-type Ca2+ channel blocker.
Amino sugar, sorbitol derivative, used as a bul...
Fermentation impurity
ALK inhibitor.
BK/SK, Kv1, Kv3, TASK-2 K+ channel blocker, vol...
T-type Ca2+ and voltage-gated Na+ channel block...
Triazole; 14-α demethylase inhibitor, voltage-...
Coumarin, more potent isomer; VKORC1 inhibitor....
Aldosterone antagonist.