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Assay Detail

CHEMBL5528524

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

Functional
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MCF7
Confidence 1 — Organism
Curated By Autocuration

Target

MCF7 (CHEMBL387)
Type CELL-LINE
Organism Homo sapiens

Publication

Design and synthesis of the first PARP-1 and proteasome dual inhibitors to treat breast cancer.
He H, Yang W, Shi Y, Chen X, Chen X, Hu X, Li X, Yang Y, Liu Z, Ye T, Wang N, Yu L.
Eur J Med Chem (2024) 264 : 115943 -115943
PubMed 38039793 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.89 7.84

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5571547 1 7.84
CHEMBL5565652 1 7.68
CHEMBL5571367 1 7.39
CHEMBL5569313 1 7.35
CHEMBL5575779 1 7.30
CHEMBL5555633 1 7.23
CHEMBL5574533 1 7.22
CHEMBL5565731 1 7.06
CHEMBL5574128 1 6.89
CHEMBL2141296 IXAZOMIB 3.0 1 6.87
CHEMBL5591486 1 6.76
CHEMBL5571281 1 6.45
CHEMBL5567244 1 6.31
CHEMBL5570683 1 6.01
CHEMBL521686 OLAPARIB 4.0 1 4.98

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5571547 IC50 = 14.6 nM 7.84
CHEMBL5565652 IC50 = 20.8 nM 7.68
CHEMBL5571367 IC50 = 40.8 nM 7.39
CHEMBL5569313 IC50 = 45.1 nM 7.35
CHEMBL5575779 IC50 = 49.5 nM 7.30
CHEMBL5555633 IC50 = 58.6 nM 7.23
CHEMBL5574533 IC50 = 60.1 nM 7.22
CHEMBL5565731 IC50 = 87.9 nM 7.06
CHEMBL5574128 IC50 = 129.9 nM 6.89
CHEMBL2141296 IXAZOMIB IC50 = 135.2 nM 6.87
CHEMBL5591486 IC50 = 173.6 nM 6.76
CHEMBL5571281 IC50 = 355.4 nM 6.45
CHEMBL5567244 IC50 = 493.3 nM 6.31
CHEMBL5570683 IC50 = 980.3 nM 6.01
CHEMBL521686 OLAPARIB IC50 = 10580.0 nM 4.98