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Assay Detail

CHEMBL3760464

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Binding
Inhibition of Vibrio cholerae beta-carbonic anhydrase using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay
40
Total Activities
40
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Vibrio cholerae
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
Del Prete S, Vullo D, De Luca V, Carginale V, Ferraroni M, Osman SM, AlOthman Z, Supuran CT, Capasso C.
Bioorg Med Chem (2016) 24 : 1115 -1120
PubMed 26850377 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 40 5.90 7.17

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL265674 1 7.17
CHEMBL6753 1 7.08
CHEMBL435 HYDROCHLOROTHIAZIDE 4.0 1 7.06
CHEMBL310671 SACCHARIN 3.0 1 6.56
CHEMBL6919 1 6.52
CHEMBL224292 1 6.46
CHEMBL7146 1 6.44
CHEMBL21 SULFANILAMIDE 4.0 1 6.35
CHEMBL328560 SULTHIAME 3.0 1 6.34
CHEMBL6852 1 6.33
CHEMBL414 CARZENIDE 2.0 1 6.29
CHEMBL269122 1 6.12
CHEMBL2324868 1 6.11
CHEMBL266026 1 6.09
CHEMBL268439 1 6.07
CHEMBL220491 BRINZOLAMIDE 4.0 1 6.07
CHEMBL73962 BENZOLAMIDE 1 6.07
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 6.06
CHEMBL220492 TOPIRAMATE 4.0 1 6.06
CHEMBL6633 1 5.65
CHEMBL17 DICHLORPHENAMIDE 4.0 1 5.63
CHEMBL6784 1 5.45
CHEMBL118 CELECOXIB 4.0 1 5.38
CHEMBL20 ACETAZOLAMIDE 4.0 1 5.35
CHEMBL2324864 1 5.35
CHEMBL266240 1 5.35
CHEMBL218490 DORZOLAMIDE 4.0 1 5.33
CHEMBL19 METHAZOLAMIDE 4.0 1 5.20
CHEMBL26 SULPIRIDE 3.0 1 5.20
CHEMBL18 ETHOXZOLAMIDE 4.0 1 5.19

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL265674 Ki = 68.1 nM 7.17
CHEMBL6753 Ki = 82.3 nM 7.08
CHEMBL435 HYDROCHLOROTHIAZIDE Ki = 87.0 nM 7.06
CHEMBL310671 SACCHARIN Ki = 275.0 nM 6.56
CHEMBL6919 Ki = 304.0 nM 6.52
CHEMBL224292 Ki = 349.0 nM 6.46
CHEMBL7146 Ki = 361.0 nM 6.44
CHEMBL21 SULFANILAMIDE Ki = 447.0 nM 6.35
CHEMBL328560 SULTHIAME Ki = 455.0 nM 6.34
CHEMBL6852 Ki = 463.0 nM 6.33
CHEMBL414 CARZENIDE Ki = 515.0 nM 6.29
CHEMBL269122 Ki = 757.0 nM 6.12
CHEMBL2324868 Ki = 785.0 nM 6.11
CHEMBL266026 Ki = 817.0 nM 6.09
CHEMBL73962 BENZOLAMIDE Ki = 846.0 nM 6.07
CHEMBL268439 Ki = 859.0 nM 6.07
CHEMBL220491 BRINZOLAMIDE Ki = 845.0 nM 6.07
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 879.0 nM 6.06
CHEMBL220492 TOPIRAMATE Ki = 874.0 nM 6.06
CHEMBL6633 Ki = 2218.0 nM 5.65
CHEMBL17 DICHLORPHENAMIDE Ki = 2352.0 nM 5.63
CHEMBL6784 Ki = 3530.0 nM 5.45
CHEMBL118 CELECOXIB Ki = 4165.0 nM 5.38
CHEMBL20 ACETAZOLAMIDE Ki = 4512.0 nM 5.35
CHEMBL2324864 Ki = 4430.0 nM 5.35
CHEMBL266240 Ki = 4450.0 nM 5.35
CHEMBL218490 DORZOLAMIDE Ki = 4728.0 nM 5.33
CHEMBL19 METHAZOLAMIDE Ki = 6260.0 nM 5.20
CHEMBL26 SULPIRIDE Ki = 6245.0 nM 5.20
CHEMBL18 ETHOXZOLAMIDE Ki = 6450.0 nM 5.19
CHEMBL77517 INDISULAM Ki = 7700.0 nM 5.11
CHEMBL865 VALDECOXIB Ki = 8200.0 nM 5.09
CHEMBL750 ZONISAMIDE Ki = 8570.0 nM 5.07
CHEMBL7092 Ki = 9120.0 nM 5.04
CHEMBL6724 Ki > 10000.0 nM -
CHEMBL574 P-TOLUENESULFONAMIDE Ki > 10000.0 nM -
CHEMBL419 MAFENIDE Ki > 10000.0 nM -
CHEMBL7087 Ki > 10000.0 nM -
CHEMBL6853 Ki > 10000.0 nM -
CHEMBL2324869 Ki > 10000.0 nM -