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Assay Detail

CHEMBL3789760

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Binding
Inhibition of recombinant Vibrio cholerae gamma-carbonic anhydrase 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

Comparison of the sulfonamide inhibition profiles of the α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
Del Prete S, Vullo D, De Luca V, Carginale V, Osman SM, AlOthman Z, Supuran CT, Capasso C.
Bioorg Med Chem Lett (2016) 26 : 1941 -1946
PubMed 26972117 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 40 6.56 7.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL265674 1 7.18
CHEMBL7087 1 7.16
CHEMBL220492 TOPIRAMATE 4.0 1 7.16
CHEMBL6753 1 7.16
CHEMBL7146 1 7.13
CHEMBL6853 1 7.13
CHEMBL7092 1 7.13
CHEMBL574 P-TOLUENESULFONAMIDE 3.0 1 7.12
CHEMBL73962 BENZOLAMIDE 1 7.11
CHEMBL26 SULPIRIDE 3.0 1 7.11
CHEMBL419 MAFENIDE 4.0 1 7.09
CHEMBL18 ETHOXZOLAMIDE 4.0 1 7.07
CHEMBL218490 DORZOLAMIDE 4.0 1 7.06
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 7.06
CHEMBL224292 1 7.05
CHEMBL77517 INDISULAM 2.0 1 7.04
CHEMBL2324868 1 7.03
CHEMBL220491 BRINZOLAMIDE 4.0 1 7.03
CHEMBL21 SULFANILAMIDE 4.0 1 7.02
CHEMBL6724 1 7.02
CHEMBL266026 1 6.56
CHEMBL328560 SULTHIAME 3.0 1 6.33
CHEMBL20 ACETAZOLAMIDE 4.0 1 6.33
CHEMBL19 METHAZOLAMIDE 4.0 1 6.31
CHEMBL435 HYDROCHLOROTHIAZIDE 4.0 1 6.30
CHEMBL2324869 1 6.26
CHEMBL310671 SACCHARIN 3.0 1 6.26
CHEMBL6919 1 6.25
CHEMBL266240 1 6.25
CHEMBL6852 1 6.17

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL265674 Ki = 66.2 nM 7.18
CHEMBL7087 Ki = 69.0 nM 7.16
CHEMBL6753 Ki = 69.9 nM 7.16
CHEMBL220492 TOPIRAMATE Ki = 68.8 nM 7.16
CHEMBL7146 Ki = 73.3 nM 7.13
CHEMBL6853 Ki = 73.6 nM 7.13
CHEMBL7092 Ki = 73.6 nM 7.13
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 76.3 nM 7.12
CHEMBL73962 BENZOLAMIDE Ki = 77.6 nM 7.11
CHEMBL26 SULPIRIDE Ki = 77.9 nM 7.11
CHEMBL419 MAFENIDE Ki = 80.6 nM 7.09
CHEMBL18 ETHOXZOLAMIDE Ki = 85.1 nM 7.07
CHEMBL218490 DORZOLAMIDE Ki = 87.3 nM 7.06
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 87.1 nM 7.06
CHEMBL224292 Ki = 88.5 nM 7.05
CHEMBL77517 INDISULAM Ki = 91.3 nM 7.04
CHEMBL2324868 Ki = 93.6 nM 7.03
CHEMBL220491 BRINZOLAMIDE Ki = 93.0 nM 7.03
CHEMBL21 SULFANILAMIDE Ki = 95.3 nM 7.02
CHEMBL6724 Ki = 95.3 nM 7.02
CHEMBL266026 Ki = 273.0 nM 6.56
CHEMBL20 ACETAZOLAMIDE Ki = 473.0 nM 6.33
CHEMBL328560 SULTHIAME Ki = 464.0 nM 6.33
CHEMBL19 METHAZOLAMIDE Ki = 494.0 nM 6.31
CHEMBL435 HYDROCHLOROTHIAZIDE Ki = 500.0 nM 6.30
CHEMBL2324869 Ki = 544.0 nM 6.26
CHEMBL310671 SACCHARIN Ki = 550.0 nM 6.26
CHEMBL6919 Ki = 556.0 nM 6.25
CHEMBL266240 Ki = 563.0 nM 6.25
CHEMBL6852 Ki = 672.0 nM 6.17
CHEMBL750 ZONISAMIDE Ki = 725.0 nM 6.14
CHEMBL2324864 Ki = 764.0 nM 6.12
CHEMBL865 VALDECOXIB Ki = 817.0 nM 6.09
CHEMBL118 CELECOXIB Ki = 834.0 nM 6.08
CHEMBL269122 Ki = 902.0 nM 6.04
CHEMBL17 DICHLORPHENAMIDE Ki = 1230.0 nM 5.91
CHEMBL6633 Ki = 4153.0 nM 5.38
CHEMBL414 CARZENIDE Ki = 5100.0 nM 5.29
CHEMBL268439 Ki = 5570.0 nM 5.25
CHEMBL6784 Ki = 6223.0 nM 5.21