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

CHEMBL828256

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

Binding
Inhibition constant against rabbit liver carboxylesterase (rCE) using nitrophenyl acetate (o-NPA) as substrate
61
Total Activities
61
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Oryctolagus cuniculus
Confidence 9 — Direct single protein target
Curated By Expert

Target

Liver carboxylesterase 1 (CHEMBL2623)
Type SINGLE PROTEIN
Organism Oryctolagus cuniculus

Publication

Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases.
Wadkins RM, Hyatt JL, Wei X, Yoon KJ, Wierdl M, Edwards CC, Morton CL, Obenauer JC, Damodaran K, Beroza P, Danks MK, Potter PM.
J Med Chem (2005) 48 : 2906 -2915
PubMed 15828829 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 61 6.89 8.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL193228 1 8.39
CHEMBL362996 1 8.21
CHEMBL191739 1 8.06
CHEMBL192139 1 8.02
CHEMBL191847 1 7.92
CHEMBL192241 1 7.82
CHEMBL192252 1 7.79
CHEMBL193229 1 7.76
CHEMBL192589 1 7.66
CHEMBL192180 1 7.62
CHEMBL191822 1 7.44
CHEMBL193180 1 7.32
CHEMBL192625 1 7.30
CHEMBL366205 1 7.27
CHEMBL192627 CHLORANIL 1 7.26
CHEMBL370059 1 7.19
CHEMBL435109 1 7.14
CHEMBL189886 BENZIL 1 6.99
CHEMBL193140 1 6.97
CHEMBL371858 1 6.92
CHEMBL192474 1 6.70
CHEMBL365392 1 6.66
CHEMBL191796 1 6.57
CHEMBL192410 1 6.40
CHEMBL365517 1 6.28
CHEMBL191513 1 6.24
CHEMBL365161 1 6.13
CHEMBL195713 1 6.08
CHEMBL364729 1 5.99
CHEMBL191676 1 5.67

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL193228 Ki = 4.1 nM 8.39
CHEMBL362996 Ki = 6.1 nM 8.21
CHEMBL191739 Ki = 8.7 nM 8.06
CHEMBL192139 Ki = 9.5 nM 8.02
CHEMBL191847 Ki = 11.9 nM 7.92
CHEMBL192241 Ki = 15.0 nM 7.82
CHEMBL192252 Ki = 16.2 nM 7.79
CHEMBL193229 Ki = 17.5 nM 7.76
CHEMBL192589 Ki = 21.7 nM 7.66
CHEMBL192180 Ki = 23.9 nM 7.62
CHEMBL191822 Ki = 36.0 nM 7.44
CHEMBL193180 Ki = 47.9 nM 7.32
CHEMBL192625 Ki = 49.6 nM 7.30
CHEMBL366205 Ki = 53.5 nM 7.27
CHEMBL192627 CHLORANIL Ki = 54.8 nM 7.26
CHEMBL370059 Ki = 64.0 nM 7.19
CHEMBL435109 Ki = 72.1 nM 7.14
CHEMBL189886 BENZIL Ki = 103.0 nM 6.99
CHEMBL193140 Ki = 108.0 nM 6.97
CHEMBL371858 Ki = 119.0 nM 6.92
CHEMBL192474 Ki = 200.0 nM 6.70
CHEMBL365392 Ki = 220.0 nM 6.66
CHEMBL191796 Ki = 267.0 nM 6.57
CHEMBL192410 Ki = 398.0 nM 6.40
CHEMBL365517 Ki = 520.0 nM 6.28
CHEMBL191513 Ki = 580.0 nM 6.24
CHEMBL365161 Ki = 736.0 nM 6.13
CHEMBL195713 Ki = 823.0 nM 6.08
CHEMBL364729 Ki = 1035.0 nM 5.99
CHEMBL191676 Ki = 2150.0 nM 5.67
CHEMBL371523 DIBENZOYLMETHANE Ki = 3950.0 nM 5.40
CHEMBL192258 Ki = 4930.0 nM 5.31
CHEMBL370299 Ki = 13900.0 nM 4.86
CHEMBL371371 Ki = 15700.0 nM 4.80
CHEMBL364734 Ki > 100000.0 nM -
CHEMBL284028 2,3-DIHYDROXY-6,7-DICHLOROQUINOXALINE Ki > 100000.0 nM -
CHEMBL192648 Ki > 100000.0 nM -
CHEMBL192595 Ki > 100000.0 nM -
CHEMBL365982 Ki > 100000.0 nM -
CHEMBL425192 Ki > 100000.0 nM -
CHEMBL190677 BENZOIN Ki > 100000.0 nM -
CHEMBL192039 Ki > 100000.0 nM -
CHEMBL192657 Ki > 100000.0 nM -
CHEMBL372856 Ki > 100000.0 nM -
CHEMBL90039 BENZOPHENONE Ki > 100000.0 nM -
CHEMBL365809 BUTANEDIONE Ki > 100000.0 nM -
CHEMBL365129 Ki > 100000.0 nM -
CHEMBL189988 BENZYLSULFONYLBENZENE Ki > 100000.0 nM -
CHEMBL190496 Ki > 100000.0 nM -
CHEMBL363855 Ki > 100000.0 nM -