Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL2380060

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

Binding
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration stopped-flow assay
40
Total Activities
40
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

The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides.
Vullo D, Luca VD, Scozzafava A, Carginale V, Rossi M, Supuran CT, Capasso C.
Bioorg Med Chem (2013) 21 : 1534 -1538
PubMed 22883029 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 40 7.32 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL13646 1 8.70
CHEMBL220491 BRINZOLAMIDE 4.0 1 8.52
CHEMBL18 ETHOXZOLAMIDE 4.0 1 8.10
CHEMBL218490 DORZOLAMIDE 4.0 1 8.05
CHEMBL73962 BENZOLAMIDE 1 8.05
CHEMBL328560 SULTHIAME 3.0 1 8.05
CHEMBL220492 TOPIRAMATE 4.0 1 8.00
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.92
CHEMBL6633 1 7.92
CHEMBL19 METHAZOLAMIDE 4.0 1 7.85
CHEMBL77517 INDISULAM 2.0 1 7.82
CHEMBL6753 1 7.72
CHEMBL14182 1 7.52
CHEMBL269122 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
CHEMBL268439 1 7.34
CHEMBL13630 1 7.30
CHEMBL6853 1 7.22
CHEMBL265674 1 7.22
CHEMBL269628 1 7.20
CHEMBL268177 1 7.16
CHEMBL266240 1 7.12
CHEMBL35118 1 7.10
CHEMBL7092 1 6.96
CHEMBL6685 1 6.90
CHEMBL6919 1 6.90

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL13646 Ki = 2.0 nM 8.70
CHEMBL220491 BRINZOLAMIDE Ki = 3.0 nM 8.52
CHEMBL18 ETHOXZOLAMIDE Ki = 8.0 nM 8.10
CHEMBL218490 DORZOLAMIDE Ki = 9.0 nM 8.05
CHEMBL73962 BENZOLAMIDE Ki = 9.0 nM 8.05
CHEMBL328560 SULTHIAME Ki = 9.0 nM 8.05
CHEMBL220492 TOPIRAMATE Ki = 10.0 nM 8.00
CHEMBL20 ACETAZOLAMIDE Ki = 12.0 nM 7.92
CHEMBL6633 Ki = 12.0 nM 7.92
CHEMBL19 METHAZOLAMIDE Ki = 14.0 nM 7.85
CHEMBL77517 INDISULAM Ki = 15.0 nM 7.82
CHEMBL6753 Ki = 19.0 nM 7.72
CHEMBL14182 Ki = 30.0 nM 7.52
CHEMBL269122 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
CHEMBL268439 Ki = 46.0 nM 7.34
CHEMBL13630 Ki = 50.0 nM 7.30
CHEMBL265674 Ki = 60.0 nM 7.22
CHEMBL6853 Ki = 60.0 nM 7.22
CHEMBL269628 Ki = 63.0 nM 7.20
CHEMBL268177 Ki = 70.0 nM 7.16
CHEMBL266240 Ki = 75.0 nM 7.12
CHEMBL35118 Ki = 80.0 nM 7.10
CHEMBL7092 Ki = 110.0 nM 6.96
CHEMBL6685 Ki = 125.0 nM 6.90
CHEMBL6919 Ki = 125.0 nM 6.90
CHEMBL287117 Ki = 133.0 nM 6.88
CHEMBL7087 Ki = 160.0 nM 6.80
CHEMBL419 MAFENIDE Ki = 170.0 nM 6.77
CHEMBL6852 Ki = 240.0 nM 6.62
CHEMBL435 HYDROCHLOROTHIAZIDE Ki = 290.0 nM 6.54
CHEMBL6705 Ki = 295.0 nM 6.53
CHEMBL21 SULFANILAMIDE Ki = 300.0 nM 6.52
CHEMBL7204 Ki = 320.0 nM 6.50
CHEMBL310671 SACCHARIN Ki = 5959.0 nM 5.22
CHEMBL118 CELECOXIB Ki = 21.0 nM -