Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL1019601

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

Binding
Inhibition of human intestinal carboxylesterase after 24 hrs
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Comparison of benzil and trifluoromethyl ketone (TFK)-mediated carboxylesterase inhibition using classical and 3D-quantitative structure-activity relationship analysis.
Harada T, Nakagawa Y, Wadkins RM, Potter PM, Wheelock CE.
Bioorg Med Chem (2009) 17 : 149 -164
PubMed 19062296 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 8.40 9.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL463556 1 9.40
CHEMBL460808 1 9.30
CHEMBL464002 1 9.30
CHEMBL460806 1 9.30
CHEMBL467450 1 9.00
CHEMBL467451 1 8.96
CHEMBL449475 1 8.92
CHEMBL89506 1 8.46
CHEMBL449775 1 8.43
CHEMBL270374 1 8.34
CHEMBL460809 1 8.32
CHEMBL270375 1 8.27
CHEMBL460807 1 8.24
CHEMBL440542 1 8.19
CHEMBL402615 1 7.78
CHEMBL510996 1 6.93
CHEMBL86668 1 5.69

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL463556 Ki = 0.3981 nM 9.40
CHEMBL460808 Ki = 0.5012 nM 9.30
CHEMBL464002 Ki = 0.5012 nM 9.30
CHEMBL460806 Ki = 0.5012 nM 9.30
CHEMBL467450 Ki = 1.0 nM 9.00
CHEMBL467451 Ki = 1.096 nM 8.96
CHEMBL449475 Ki = 1.202 nM 8.92
CHEMBL89506 Ki = 3.467 nM 8.46
CHEMBL449775 Ki = 3.715 nM 8.43
CHEMBL270374 Ki = 4.571 nM 8.34
CHEMBL460809 Ki = 4.786 nM 8.32
CHEMBL270375 Ki = 5.37 nM 8.27
CHEMBL460807 Ki = 5.754 nM 8.24
CHEMBL440542 Ki = 6.457 nM 8.19
CHEMBL402615 Ki = 16.6 nM 7.78
CHEMBL510996 Ki = 117.49 nM 6.93
CHEMBL86668 Ki = 2041.74 nM 5.69