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Assay Detail

CHEMBL4146960

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

ADMET
Cytotoxicity against human K562 cells assessed as reduction in cell viability after 72 hrs by MTS assay
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Cell Type K562
Confidence 1 — Organism
Curated By Intermediate

Target

K562 (CHEMBL385)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and biological evaluation of bifendate derivatives bearing 6,7-dihydro-dibenzo[c,e]azepine scaffold as potential P-glycoprotein and tumor metastasis inhibitors.
Gu X, Jiang Y, Qu Y, Chen J, Feng D, Li C, Yin X.
Eur J Med Chem (2018) 145 : 379 -388
PubMed 29335204 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 4.91 6.41

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL359744 DOXORUBICIN HYDROCHLORIDE 4.0 1 6.41
CHEMBL4170740 1 5.29
CHEMBL4162802 1 5.23
CHEMBL4167348 1 5.09
CHEMBL4162271 1 4.96
CHEMBL4159444 1 4.93
CHEMBL4160523 1 4.90
CHEMBL4171124 1 4.86
CHEMBL4172945 1 4.85
CHEMBL4172197 1 4.84
CHEMBL4174561 1 4.82
CHEMBL4164308 1 4.77
CHEMBL4176636 1 4.64
CHEMBL4168776 1 4.53
CHEMBL4163907 1 4.52
CHEMBL4161527 1 4.46
CHEMBL2012363 1 4.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL359744 DOXORUBICIN HYDROCHLORIDE IC50 = 390.0 nM 6.41
CHEMBL4170740 IC50 = 5070.0 nM 5.29
CHEMBL4162802 IC50 = 5850.0 nM 5.23
CHEMBL4167348 IC50 = 8180.0 nM 5.09
CHEMBL4162271 IC50 = 10960.0 nM 4.96
CHEMBL4159444 IC50 = 11820.0 nM 4.93
CHEMBL4160523 IC50 = 12540.0 nM 4.90
CHEMBL4171124 IC50 = 13670.0 nM 4.86
CHEMBL4172945 IC50 = 14110.0 nM 4.85
CHEMBL4172197 IC50 = 14440.0 nM 4.84
CHEMBL4174561 IC50 = 15030.0 nM 4.82
CHEMBL4164308 IC50 = 16870.0 nM 4.77
CHEMBL4176636 IC50 = 23050.0 nM 4.64
CHEMBL4168776 IC50 = 29820.0 nM 4.53
CHEMBL4163907 IC50 = 30490.0 nM 4.52
CHEMBL4161527 IC50 = 34780.0 nM 4.46
CHEMBL2012363 IC50 = 51350.0 nM 4.29