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Assay Detail

CHEMBL5362173

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

Binding
Inhibition of PARP1 (unknown origin)
10
Total Activities
10
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

Poly [ADP-ribose] polymerase 1 (CHEMBL3105)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

An overview of compound properties, multiparameter optimization, and computational drug design methods for PARP-1 inhibitor drugs.
Hirlekar BU, Nuthi A, Singh KD, Murty US, Dixit VA.
Eur J Med Chem (2023) 252 : 115300 -115300
PubMed 36989813 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 8.45 10.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5396891 1 10.64
CHEMBL506871 VELIPARIB 3.0 1 10.21
CHEMBL3137320 TALAZOPARIB 4.0 1 8.96
CHEMBL521686 OLAPARIB 4.0 1 8.85
CHEMBL1173055 RUCAPARIB 4.0 1 8.49
CHEMBL4458889 1 7.89
CHEMBL1094636 NIRAPARIB 4.0 1 7.78
CHEMBL5274451 1 7.72
CHEMBL4590570 1 7.72
CHEMBL2347906 1 6.28

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5396891 IC50 = 0.023 nM 10.64
CHEMBL506871 VELIPARIB IC50 = 0.061 nM 10.21
CHEMBL3137320 TALAZOPARIB IC50 = 1.1 nM 8.96
CHEMBL521686 OLAPARIB IC50 = 1.4 nM 8.85
CHEMBL1173055 RUCAPARIB IC50 = 3.2 nM 8.49
CHEMBL4458889 IC50 = 13.0 nM 7.89
CHEMBL1094636 NIRAPARIB IC50 = 16.7 nM 7.78
CHEMBL5274451 IC50 = 19.0 nM 7.72
CHEMBL4590570 IC50 = 19.0 nM 7.72
CHEMBL2347906 IC50 = 530.0 nM 6.28