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Assay Detail

CHEMBL3131237

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

Binding
Inhibition of Escherichia coli FabH expressed in Escherichia coli BL21 (DE3) after 25 mins
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Escherichia coli
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design and synthesis of 2-styryl of 5-Nitroimidazole derivatives and antimicrobial activities as FabH inhibitors.
Duan YT, Wang ZC, Sang YL, Tao XX, Teraiya SB, Wang PF, Wen Q, Zhou XJ, Ding L, Yang YH, Zhu HL.
Eur J Med Chem (2014) 76 : 387 -396
PubMed 24594526 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 5.26 5.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3127229 1 5.68
CHEMBL1384 KANAMYCIN 4.0 1 5.51
CHEMBL3127243 1 5.47
CHEMBL3127232 1 5.38
CHEMBL3127233 1 5.36
CHEMBL3127234 1 5.19
CHEMBL3127238 1 4.99
CHEMBL3127242 1 4.96
CHEMBL3127226 1 4.78

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3127229 IC50 = 2100.0 nM 5.68
CHEMBL1384 KANAMYCIN IC50 = 3100.0 nM 5.51
CHEMBL3127243 IC50 = 3400.0 nM 5.47
CHEMBL3127232 IC50 = 4200.0 nM 5.38
CHEMBL3127233 IC50 = 4400.0 nM 5.36
CHEMBL3127234 IC50 = 6500.0 nM 5.19
CHEMBL3127238 IC50 = 10200.0 nM 4.99
CHEMBL3127242 IC50 = 11000.0 nM 4.96
CHEMBL3127226 IC50 = 16500.0 nM 4.78