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Assay Detail

CHEMBL5317577

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

Binding
Inhibition of human recombinant N-terminal FLAG-tagged PARP7 (400 to 657 end residues) incubated for 1 hr by ELISA assay
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

Protein mono-ADP-ribosyltransferase TIPARP (CHEMBL2380188)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of the Potent and Highly Selective PARP7 Inhibitor as a Novel Immunotherapeutic Agent for Tumors.
Gu H, Yan W, Wang Y, Xu W, Huang L, Yang J, Zhai B, Wang H, Su Y, Zhu Q, Liu B, Hao H, Zou Y, Xu Y.
J Med Chem (2023) 66 : 473 -490
PubMed 36576395 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 8.21 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5095043 ATAMPARIB 1.0 1 8.30
CHEMBL5395820 1 8.12

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5095043 ATAMPARIB IC50 = 5.0 nM 8.30
CHEMBL5395820 IC50 = 7.6 nM 8.12