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Assay Detail

CHEMBL3270420

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

Binding
Inhibition of Helicobacter pylori carbonic anhydrase by stopped-flow CO2 hydration assay
40
Total Activities
40
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Helicobacter pylori
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila.
Nishimori I, Vullo D, Minakuchi T, Scozzafava A, Capasso C, Supuran CT.
Bioorg Med Chem (2014) 22 : 2939 -2946
PubMed 24792813 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 40 6.58 7.50

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL220492 TOPIRAMATE 4.0 1 7.50
CHEMBL18 ETHOXZOLAMIDE 4.0 1 7.48
CHEMBL26 SULPIRIDE 3.0 1 7.46
CHEMBL6633 1 7.42
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.40
CHEMBL73962 BENZOLAMIDE 1 7.27
CHEMBL268439 1 7.19
CHEMBL7146 1 7.15
CHEMBL218490 DORZOLAMIDE 4.0 1 7.14
CHEMBL266026 1 7.06
CHEMBL17 DICHLORPHENAMIDE 4.0 1 6.98
CHEMBL220491 BRINZOLAMIDE 4.0 1 6.89
CHEMBL77517 INDISULAM 2.0 1 6.84
CHEMBL19 METHAZOLAMIDE 4.0 1 6.75
CHEMBL6784 1 6.66
CHEMBL6919 1 6.63
CHEMBL750 ZONISAMIDE 4.0 1 6.59
CHEMBL414 CARZENIDE 2.0 1 6.35
CHEMBL266240 1 6.19
CHEMBL6753 1 6.12
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 6.01
CHEMBL6724 1 5.91
CHEMBL6853 1 5.87
CHEMBL7092 1 5.83
CHEMBL21 SULFANILAMIDE 4.0 1 5.73
CHEMBL419 MAFENIDE 4.0 1 5.63
CHEMBL574 P-TOLUENESULFONAMIDE 3.0 1 5.61
CHEMBL265674 1 5.59
CHEMBL7087 1 5.46
CHEMBL310671 SACCHARIN 3.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL220492 TOPIRAMATE Ki = 32.0 nM 7.50
CHEMBL18 ETHOXZOLAMIDE Ki = 33.0 nM 7.48
CHEMBL26 SULPIRIDE Ki = 35.0 nM 7.46
CHEMBL6633 Ki = 38.0 nM 7.42
CHEMBL20 ACETAZOLAMIDE Ki = 40.0 nM 7.40
CHEMBL73962 BENZOLAMIDE Ki = 54.0 nM 7.27
CHEMBL268439 Ki = 64.0 nM 7.19
CHEMBL7146 Ki = 71.0 nM 7.15
CHEMBL218490 DORZOLAMIDE Ki = 73.0 nM 7.14
CHEMBL266026 Ki = 87.0 nM 7.06
CHEMBL17 DICHLORPHENAMIDE Ki = 105.0 nM 6.98
CHEMBL220491 BRINZOLAMIDE Ki = 128.0 nM 6.89
CHEMBL77517 INDISULAM Ki = 143.0 nM 6.84
CHEMBL19 METHAZOLAMIDE Ki = 176.0 nM 6.75
CHEMBL6784 Ki = 218.0 nM 6.66
CHEMBL6919 Ki = 236.0 nM 6.63
CHEMBL750 ZONISAMIDE Ki = 254.0 nM 6.59
CHEMBL414 CARZENIDE Ki = 450.0 nM 6.35
CHEMBL266240 Ki = 640.0 nM 6.19
CHEMBL6753 Ki = 768.0 nM 6.12
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 973.0 nM 6.01
CHEMBL6724 Ki = 1235.0 nM 5.91
CHEMBL6853 Ki = 1359.0 nM 5.87
CHEMBL7092 Ki = 1463.0 nM 5.83
CHEMBL21 SULFANILAMIDE Ki = 1845.0 nM 5.73
CHEMBL419 MAFENIDE Ki = 2360.0 nM 5.63
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 2470.0 nM 5.61
CHEMBL265674 Ki = 2590.0 nM 5.59
CHEMBL7087 Ki = 3500.0 nM 5.46
CHEMBL2324868 Ki - -
CHEMBL2324869 Ki - -
CHEMBL224292 Ki - -
CHEMBL2324864 Ki - -
CHEMBL269122 Ki - -
CHEMBL328560 SULTHIAME Ki - -
CHEMBL118 CELECOXIB Ki - -
CHEMBL865 VALDECOXIB Ki - -
CHEMBL435 HYDROCHLOROTHIAZIDE Ki - -
CHEMBL6852 Ki - -
CHEMBL310671 SACCHARIN Ki - -