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Assay Detail

CHEMBL2049249

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

Binding
Inhibition of human carbonic anhydrase 2 preincubated for 15 mins measured for 10 to 100 sec by stopped-flow method
41
Total Activities
41
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Carbonic anhydrase 2 (CHEMBL205)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Molecular cloning, characterization, and inhibition studies of a β-carbonic anhydrase from Malassezia globosa, a potential antidandruff target.
Hewitson KS, Vullo D, Scozzafava A, Mastrolorenzo A, Supuran CT.
J Med Chem (2012) 55 : 3513 -3520
PubMed 22424239 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 41 7.45 8.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL24259 PHENYLSULFAMATE 1 8.89
CHEMBL283121 1 8.82
CHEMBL268439 1 8.70
CHEMBL220491 BRINZOLAMIDE 4.0 1 8.52
CHEMBL18 ETHOXZOLAMIDE 4.0 1 8.10
CHEMBL73962 BENZOLAMIDE 1 8.05
CHEMBL218490 DORZOLAMIDE 4.0 1 8.05
CHEMBL220492 TOPIRAMATE 4.0 1 8.00
CHEMBL360356 1 7.92
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.92
CHEMBL168514 PHENYLSULFAMIDE 1 7.89
CHEMBL19 METHAZOLAMIDE 4.0 1 7.85
CHEMBL77517 INDISULAM 2.0 1 7.82
CHEMBL6753 1 7.72
CHEMBL166686 1 7.64
CHEMBL6633 1 7.48
CHEMBL750 ZONISAMIDE 4.0 1 7.46
CHEMBL17 DICHLORPHENAMIDE 4.0 1 7.42
CHEMBL6724 1 7.40
CHEMBL26 SULPIRIDE 3.0 1 7.40
CHEMBL865 VALDECOXIB 4.0 1 7.37
CHEMBL266026 1 7.34
CHEMBL7146 1 7.30
CHEMBL265674 1 7.22
CHEMBL6853 1 7.22
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 7.20
CHEMBL268177 1 7.16
CHEMBL266240 1 7.12
CHEMBL6919 1 7.10
CHEMBL178852 1 7.09

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL24259 PHENYLSULFAMATE Ki = 1.3 nM 8.89
CHEMBL283121 Ki = 1.5 nM 8.82
CHEMBL268439 Ki = 2.0 nM 8.70
CHEMBL220491 BRINZOLAMIDE Ki = 3.0 nM 8.52
CHEMBL18 ETHOXZOLAMIDE Ki = 8.0 nM 8.10
CHEMBL73962 BENZOLAMIDE Ki = 9.0 nM 8.05
CHEMBL218490 DORZOLAMIDE Ki = 9.0 nM 8.05
CHEMBL220492 TOPIRAMATE Ki = 10.0 nM 8.00
CHEMBL360356 Ki = 12.0 nM 7.92
CHEMBL20 ACETAZOLAMIDE Ki = 12.0 nM 7.92
CHEMBL168514 PHENYLSULFAMIDE Ki = 13.0 nM 7.89
CHEMBL19 METHAZOLAMIDE Ki = 14.0 nM 7.85
CHEMBL77517 INDISULAM Ki = 15.0 nM 7.82
CHEMBL6753 Ki = 19.0 nM 7.72
CHEMBL166686 Ki = 23.0 nM 7.64
CHEMBL6633 Ki = 33.0 nM 7.48
CHEMBL750 ZONISAMIDE Ki = 35.0 nM 7.46
CHEMBL17 DICHLORPHENAMIDE Ki = 38.0 nM 7.42
CHEMBL6724 Ki = 40.0 nM 7.40
CHEMBL26 SULPIRIDE Ki = 40.0 nM 7.40
CHEMBL865 VALDECOXIB Ki = 43.0 nM 7.37
CHEMBL266026 Ki = 46.0 nM 7.34
CHEMBL7146 Ki = 50.0 nM 7.30
CHEMBL265674 Ki = 60.0 nM 7.22
CHEMBL6853 Ki = 60.0 nM 7.22
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 63.0 nM 7.20
CHEMBL268177 Ki = 70.0 nM 7.16
CHEMBL266240 Ki = 75.0 nM 7.12
CHEMBL6919 Ki = 80.0 nM 7.10
CHEMBL178852 Ki = 81.0 nM 7.09
CHEMBL7092 Ki = 110.0 nM 6.96
CHEMBL6784 Ki = 125.0 nM 6.90
CHEMBL414 CARZENIDE Ki = 133.0 nM 6.88
CHEMBL7087 Ki = 160.0 nM 6.80
CHEMBL419 MAFENIDE Ki = 170.0 nM 6.77
CHEMBL21 SULFANILAMIDE Ki = 240.0 nM 6.62
CHEMBL6705 Ki = 295.0 nM 6.53
CHEMBL27601 BENZENESULFONAMIDE Ki = 305.0 nM 6.52
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 320.0 nM 6.50
CHEMBL451332 Ki = 495.0 nM 6.30
CHEMBL118 CELECOXIB Ki = 21.0 nM -