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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T6820 | D-α-Hydroxyglutaric acid disodium | D-alpha-Hydroxyglutaric acid disodium salt,Disodium (R)-2-Hydroxyglutarate | ATPase , Others , Reactive Oxygen Species , Endogenous Metabolite , mTOR |
D-α-Hydroxyglutaric acid disodium (Disodium (R)-2-Hydroxyglutarate) is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases with Ki of 0.628 mM. | |||
T79745 | IDH2R140Q-IN-2 | Dehydrogenase | |
IDH2R140Q-IN-2 is an orally active and potent IDH2R140Q inhibitor with an IC50 of 29 nM.IDH2R140Q-IN-2 possesses potential antitumour activity, reducing D2HG production in TF-1 cell lines carrying the IDH2R140Q mutation ... | |||
T63193 | IDH2R140Q-IN-1 | ||
IDH2R140Q-IN-1 is a potent inhibitor of IDH2R140Q (IC50: 6.1 nM) and can be used in studies of acute myeloid leukemia. | |||
T2346 | Enasidenib | AG-221 | Dehydrogenase , Isocitrate Dehydrogenase (IDH) |
Enasidenib (AG-221) is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity. | |||
T1809 | AGI-6780 | Dehydrogenase , Isocitrate Dehydrogenase (IDH) | |
AGI-6780 is a potent and selective inhibitor of IDH2 R140Q mutant. | |||
T2346L | Enasidenib mesylate | AG221 mesylate,AG 221 mesylate,AG-221 mesylate | Dehydrogenase |
Enasidenib mesylate (AG-221 mesylate) is a potent and selective IDH2 mutase inhibitor that promotes differentiation of leukemia myeloid cells for the treatment of acute myeloid leukemia. | |||
T7307 | Vorasidenib | PVM/MA,AG-881 | Isocitrate Dehydrogenase (IDH) |
Vorasidenib (PVM/MA) is an inhibitor of mutant isocitrate dehydrogenase (IDH; IC50s = 31.9 and 31.7 nM for IDH1R132H and IDH2R140Q, respectively) | |||
T39716 | Mutant IDH1-IN-6 | Mutant IDH1-IN-6 | |
Mutant IDH1-IN-6 is an orally active compound that effectively inhibits mutant isocitrate dehydrogenase (IDH) enzymes. It demonstrates potency and selectivity, with IC50 values of 6.27, 3.71, 36.9, and 11.5 nM for IDH1 R... | |||
T63402 | (S,R)-WT IDH1 Inhibitor 2 | ||
(S,R)-WT IDH1 Inhibitor 2 is a selective and potent mutant IDH1 inhibitor that inhibits R132G (IC50: 2.9 nM), R132C (IC50: 3.8 nM), R132H (IC50: 4.6 nM) and WT IDH1 (IC50: 46 nM) with 100-fold higher selectivity than IDH... | |||
T78758 | IHMT-IDH1-053 | Isocitrate Dehydrogenase (IDH) | |
IHMT-IDH1-053 (compound 16) is an irreversible inhibitor exhibiting high selectivity for the IDH1 R132H mutant, achieving an IC50 of 4.7 nM. It preferentially targets IDH1 mutants over wild-type IDH1 and IDH2, both wild-... |