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Assay Detail

CHEMBL5368518

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of wildtype IDH2 (unknown origin)
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Isocitrate dehydrogenase [NADP], mitochondrial (CHEMBL3991501)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Based Drug Design of Novel Triaminotriazine Derivatives as Orally Bioavailable IDH2<sup>R140Q</sup> Inhibitors with High Selectivity and Reduced hERG Inhibitory Activity for the Treatment of Acute Myeloid Leukemia.
Wei Q, Yao K, Yang J, Zhou Q, Liu P, Chen J, Liu H, Lai Y, Cao P.
J Med Chem (2023) 66 : 12894 -12910
PubMed 37706660 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 6.72 6.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3392845 1 6.72
CHEMBL5415614 1 6.71

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3392845 IC50 = 190.0 nM 6.72
CHEMBL5415614 IC50 = 196.2 nM 6.71