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Assay Detail

CHEMBL5507502

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

Binding
Binding affinity to menin (unknown origin) incubated for 1 hr by fluorescence polarization assay
15
Total Activities
15
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

Menin (CHEMBL1615381)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of novel pyrrolo[2,3-d]pyrimidines as potent menin-mixed lineage leukemia interaction inhibitors.
Bai H, Yang Z, Lei H, Wu Y, Liu J, Yuan B, Ma M, Gao L, Zhang SQ, Xin M.
Eur J Med Chem (2024) 268 : 116226 -116226
PubMed 38367493 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.18 6.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5565919 1 6.60
CHEMBL5527907 1 6.42
CHEMBL5555656 1 6.35
CHEMBL5557085 1 6.33
CHEMBL5557705 1 6.28
CHEMBL3586089 1 6.22
CHEMBL5518084 1 6.14
CHEMBL5560342 1 5.98
CHEMBL5562800 1 5.94
CHEMBL5559575 1 5.91
CHEMBL5558500 1 5.83
CHEMBL5557241 1 -
CHEMBL5560540 1 -
CHEMBL5532611 1 -
CHEMBL5566849 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5565919 IC50 = 250.0 nM 6.60
CHEMBL5527907 IC50 = 380.0 nM 6.42
CHEMBL5555656 IC50 = 450.0 nM 6.35
CHEMBL5557085 IC50 = 470.0 nM 6.33
CHEMBL5557705 IC50 = 530.0 nM 6.28
CHEMBL3586089 IC50 = 600.0 nM 6.22
CHEMBL5518084 IC50 = 730.0 nM 6.14
CHEMBL5560342 IC50 = 1040.0 nM 5.98
CHEMBL5562800 IC50 = 1140.0 nM 5.94
CHEMBL5559575 IC50 = 1220.0 nM 5.91
CHEMBL5558500 IC50 = 1470.0 nM 5.83
CHEMBL5557241 IC50 > 10000.0 nM -
CHEMBL5560540 IC50 > 10000.0 nM -
CHEMBL5532611 IC50 > 10000.0 nM -
CHEMBL5566849 IC50 > 10000.0 nM -