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Assay Detail

CHEMBL1678666

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Binding
Inhibition of Brucella suis carbonic anhydrase II 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 6.53 8.14

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1672445 1 8.14
CHEMBL1090523 1 8.00
CHEMBL6753 1 7.95
CHEMBL1089967 1 7.84
CHEMBL306195 1 7.22
CHEMBL7146 1 7.17
CHEMBL7092 1 7.10
CHEMBL26 SULPIRIDE 3.0 1 7.08
CHEMBL6853 1 7.08
CHEMBL67755 1 7.08
CHEMBL6685 1 7.08
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 7.06
CHEMBL51668 1 7.05
CHEMBL266026 1 7.03
CHEMBL220492 TOPIRAMATE 4.0 1 7.00
CHEMBL268439 1 6.97
CHEMBL17 DICHLORPHENAMIDE 4.0 1 6.95
CHEMBL73962 BENZOLAMIDE 1 6.93
CHEMBL77517 INDISULAM 2.0 1 6.89
CHEMBL118 CELECOXIB 4.0 1 6.89
CHEMBL360356 1 6.78
CHEMBL182455 1 6.71
CHEMBL23350 1 6.67
CHEMBL20 ACETAZOLAMIDE 4.0 1 6.52
CHEMBL750 ZONISAMIDE 4.0 1 6.39
CHEMBL18 ETHOXZOLAMIDE 4.0 1 6.38
CHEMBL865 VALDECOXIB 4.0 1 6.21
CHEMBL220491 BRINZOLAMIDE 4.0 1 6.20
CHEMBL19 METHAZOLAMIDE 4.0 1 6.19
CHEMBL71611 1 6.18

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1672445 Ki = 7.3 nM 8.14
CHEMBL1090523 Ki = 10.1 nM 8.00
CHEMBL6753 Ki = 11.2 nM 7.95
CHEMBL1089967 Ki = 14.6 nM 7.84
CHEMBL306195 Ki = 60.0 nM 7.22
CHEMBL7146 Ki = 68.0 nM 7.17
CHEMBL7092 Ki = 79.0 nM 7.10
CHEMBL26 SULPIRIDE Ki = 84.0 nM 7.08
CHEMBL6853 Ki = 83.0 nM 7.08
CHEMBL67755 Ki = 84.0 nM 7.08
CHEMBL6685 Ki = 83.0 nM 7.08
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 87.0 nM 7.06
CHEMBL51668 Ki = 90.0 nM 7.05
CHEMBL266026 Ki = 94.0 nM 7.03
CHEMBL220492 TOPIRAMATE Ki = 99.0 nM 7.00
CHEMBL268439 Ki = 108.0 nM 6.97
CHEMBL17 DICHLORPHENAMIDE Ki = 112.0 nM 6.95
CHEMBL73962 BENZOLAMIDE Ki = 117.0 nM 6.93
CHEMBL77517 INDISULAM Ki = 130.0 nM 6.89
CHEMBL118 CELECOXIB Ki = 128.0 nM 6.89
CHEMBL360356 Ki = 166.0 nM 6.78
CHEMBL182455 Ki = 193.0 nM 6.71
CHEMBL23350 Ki = 215.0 nM 6.67
CHEMBL20 ACETAZOLAMIDE Ki = 303.0 nM 6.52
CHEMBL750 ZONISAMIDE Ki = 406.0 nM 6.39
CHEMBL18 ETHOXZOLAMIDE Ki = 420.0 nM 6.38
CHEMBL865 VALDECOXIB Ki = 612.0 nM 6.21
CHEMBL220491 BRINZOLAMIDE Ki = 625.0 nM 6.20
CHEMBL19 METHAZOLAMIDE Ki = 642.0 nM 6.19
CHEMBL71611 Ki = 663.0 nM 6.18
CHEMBL414 CARZENIDE Ki = 697.0 nM 6.16
CHEMBL266240 Ki = 691.0 nM 6.16
CHEMBL6919 Ki = 758.0 nM 6.12
CHEMBL6633 Ki = 769.0 nM 6.11
CHEMBL265674 Ki = 847.0 nM 6.07
CHEMBL218490 DORZOLAMIDE Ki = 923.0 nM 6.04
CHEMBL7204 Ki = 4763.0 nM 5.32
CHEMBL6705 Ki = 5048.0 nM 5.30
CHEMBL6784 Ki = 5130.0 nM 5.29
CHEMBL21 SULFANILAMIDE Ki = 5080.0 nM 5.29
CHEMBL176495 Ki = 5639.0 nM 5.25
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 5560.0 nM 5.25
CHEMBL419 MAFENIDE Ki = 5910.0 nM 5.23
CHEMBL7087 Ki = 8560.0 nM 5.07