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Assay Detail

CHEMBL3591401

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

Binding
Binding affinity to TAF1 in human HUT78 cells incubated for 45 mins by mass spectrometry based bromosphere chemoproteomic assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HuT78
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Transcription initiation factor TFIID subunit 1 (CHEMBL3217390)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Based Optimization of Naphthyridones into Potent ATAD2 Bromodomain Inhibitors.
Bamborough P, Chung CW, Furze RC, Grandi P, Michon AM, Sheppard RJ, Barnett H, Diallo H, Dixon DP, Douault C, Jones EJ, Karamshi B, Mitchell DJ, Prinjha RK, Rau C, Watson RJ, Werner T, Demont EH.
J Med Chem (2015) 58 : 6151 -6178
PubMed 26230603 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 3 5.40 5.90

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3590408 1 5.90
CHEMBL3590405 1 5.80
CHEMBL3590389 1 4.50

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3590408 Kd = 1258.93 nM 5.90
CHEMBL3590405 Kd = 1584.89 nM 5.80
CHEMBL3590389 Kd = 31622.78 nM 4.50