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Assay Detail

CHEMBL1678667

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Binding
Inhibition of Brucella suis carbonic anhydrase I by spectrophotometry at pH 8.3
44
Total Activities
44
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Brucella suis
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

A new β-carbonic anhydrase from Brucella suis, its cloning, characterization, and inhibition with sulfonamides and sulfamates, leading to impaired pathogen growth.
Joseph P, Ouahrani-Bettache S, Montero JL, Nishimori I, Minakuchi T, Vullo D, Scozzafava A, Winum JY, Köhler S, Supuran CT.
Bioorg Med Chem (2011) 19 : 1172 -1178
PubMed 21251841 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 44 6.74 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1089967 1 8.05
CHEMBL1090523 1 8.04
CHEMBL18 ETHOXZOLAMIDE 4.0 1 7.77
CHEMBL118 CELECOXIB 4.0 1 7.75
CHEMBL865 VALDECOXIB 4.0 1 7.72
CHEMBL1672445 1 7.72
CHEMBL26 SULPIRIDE 3.0 1 7.72
CHEMBL218490 DORZOLAMIDE 4.0 1 7.68
CHEMBL6633 1 7.68
CHEMBL220491 BRINZOLAMIDE 4.0 1 7.58
CHEMBL51668 1 7.57
CHEMBL360356 1 7.48
CHEMBL6685 1 7.32
CHEMBL77517 INDISULAM 2.0 1 7.30
CHEMBL19 METHAZOLAMIDE 4.0 1 7.27
CHEMBL17 DICHLORPHENAMIDE 4.0 1 7.24
CHEMBL220492 TOPIRAMATE 4.0 1 7.24
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.20
CHEMBL268439 1 7.16
CHEMBL73962 BENZOLAMIDE 1 7.12
CHEMBL182455 1 7.12
CHEMBL23350 1 7.10
CHEMBL71611 1 6.73
CHEMBL306195 1 6.61
CHEMBL414 CARZENIDE 2.0 1 6.47
CHEMBL67755 1 6.46
CHEMBL7146 1 6.13
CHEMBL6919 1 6.12
CHEMBL419 MAFENIDE 4.0 1 6.12
CHEMBL7092 1 6.10

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1089967 Ki = 8.9 nM 8.05
CHEMBL1090523 Ki = 9.2 nM 8.04
CHEMBL18 ETHOXZOLAMIDE Ki = 17.0 nM 7.77
CHEMBL118 CELECOXIB Ki = 18.0 nM 7.75
CHEMBL865 VALDECOXIB Ki = 19.0 nM 7.72
CHEMBL1672445 Ki = 19.0 nM 7.72
CHEMBL26 SULPIRIDE Ki = 19.0 nM 7.72
CHEMBL218490 DORZOLAMIDE Ki = 21.0 nM 7.68
CHEMBL6633 Ki = 21.0 nM 7.68
CHEMBL220491 BRINZOLAMIDE Ki = 26.0 nM 7.58
CHEMBL51668 Ki = 27.0 nM 7.57
CHEMBL360356 Ki = 33.0 nM 7.48
CHEMBL6685 Ki = 48.0 nM 7.32
CHEMBL77517 INDISULAM Ki = 50.0 nM 7.30
CHEMBL19 METHAZOLAMIDE Ki = 54.0 nM 7.27
CHEMBL17 DICHLORPHENAMIDE Ki = 58.0 nM 7.24
CHEMBL220492 TOPIRAMATE Ki = 57.0 nM 7.24
CHEMBL20 ACETAZOLAMIDE Ki = 63.0 nM 7.20
CHEMBL268439 Ki = 70.0 nM 7.16
CHEMBL73962 BENZOLAMIDE Ki = 75.0 nM 7.12
CHEMBL182455 Ki = 75.0 nM 7.12
CHEMBL23350 Ki = 79.0 nM 7.10
CHEMBL71611 Ki = 186.0 nM 6.73
CHEMBL306195 Ki = 243.0 nM 6.61
CHEMBL414 CARZENIDE Ki = 340.0 nM 6.47
CHEMBL67755 Ki = 345.0 nM 6.46
CHEMBL7146 Ki = 745.0 nM 6.13
CHEMBL6919 Ki = 754.0 nM 6.12
CHEMBL419 MAFENIDE Ki = 768.0 nM 6.12
CHEMBL7092 Ki = 800.0 nM 6.10
CHEMBL6784 Ki = 865.0 nM 6.06
CHEMBL7087 Ki = 880.0 nM 6.06
CHEMBL266240 Ki = 940.0 nM 6.03
CHEMBL176495 Ki = 1035.0 nM 5.99
CHEMBL266026 Ki = 1050.0 nM 5.98
CHEMBL6853 Ki = 1070.0 nM 5.97
CHEMBL265674 Ki = 1210.0 nM 5.92
CHEMBL6753 Ki = 1430.0 nM 5.84
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 1580.0 nM 5.80
CHEMBL750 ZONISAMIDE Ki = 1850.0 nM 5.73
CHEMBL7204 Ki = 2400.0 nM 5.62
CHEMBL21 SULFANILAMIDE Ki = 2500.0 nM 5.60
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 4830.0 nM 5.32
CHEMBL6705 Ki = 5870.0 nM 5.23