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

CHEMBL2380058

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

Binding
Inhibition of Sulfurihydrogenibium yellowstonense YO3AOP1 recombinant carbonic anhydrase 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 Sulfurihydrogenibium yellowstonense
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

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 7.31 8.35

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL20 ACETAZOLAMIDE 4.0 1 8.35
CHEMBL865 VALDECOXIB 4.0 1 8.28
CHEMBL13646 1 8.26
CHEMBL269122 1 8.19
CHEMBL220492 TOPIRAMATE 4.0 1 8.18
CHEMBL118 CELECOXIB 4.0 1 8.16
CHEMBL435 HYDROCHLOROTHIAZIDE 4.0 1 8.14
CHEMBL268439 1 8.11
CHEMBL328560 SULTHIAME 3.0 1 8.11
CHEMBL218490 DORZOLAMIDE 4.0 1 8.10
CHEMBL73962 BENZOLAMIDE 1 8.09
CHEMBL19 METHAZOLAMIDE 4.0 1 8.09
CHEMBL17 DICHLORPHENAMIDE 4.0 1 8.07
CHEMBL18 ETHOXZOLAMIDE 4.0 1 8.03
CHEMBL13630 1 8.01
CHEMBL220491 BRINZOLAMIDE 4.0 1 7.91
CHEMBL7092 1 7.38
CHEMBL268177 1 7.35
CHEMBL269628 1 7.21
CHEMBL14182 1 7.18
CHEMBL26 SULPIRIDE 3.0 1 7.17
CHEMBL6853 1 7.17
CHEMBL6633 1 7.15
CHEMBL287117 1 7.14
CHEMBL7087 1 7.14
CHEMBL6724 1 7.12
CHEMBL77517 INDISULAM 2.0 1 7.08
CHEMBL266240 1 7.06
CHEMBL265674 1 6.86
CHEMBL750 ZONISAMIDE 4.0 1 6.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL20 ACETAZOLAMIDE Ki = 4.5 nM 8.35
CHEMBL865 VALDECOXIB Ki = 5.3 nM 8.28
CHEMBL13646 Ki = 5.5 nM 8.26
CHEMBL269122 Ki = 6.5 nM 8.19
CHEMBL220492 TOPIRAMATE Ki = 6.6 nM 8.18
CHEMBL118 CELECOXIB Ki = 6.9 nM 8.16
CHEMBL435 HYDROCHLOROTHIAZIDE Ki = 7.2 nM 8.14
CHEMBL268439 Ki = 7.8 nM 8.11
CHEMBL328560 SULTHIAME Ki = 7.8 nM 8.11
CHEMBL218490 DORZOLAMIDE Ki = 8.0 nM 8.10
CHEMBL19 METHAZOLAMIDE Ki = 8.2 nM 8.09
CHEMBL73962 BENZOLAMIDE Ki = 8.1 nM 8.09
CHEMBL17 DICHLORPHENAMIDE Ki = 8.5 nM 8.07
CHEMBL18 ETHOXZOLAMIDE Ki = 9.3 nM 8.03
CHEMBL13630 Ki = 9.7 nM 8.01
CHEMBL220491 BRINZOLAMIDE Ki = 12.3 nM 7.91
CHEMBL7092 Ki = 41.2 nM 7.38
CHEMBL268177 Ki = 44.8 nM 7.35
CHEMBL269628 Ki = 61.2 nM 7.21
CHEMBL14182 Ki = 66.4 nM 7.18
CHEMBL26 SULPIRIDE Ki = 67.4 nM 7.17
CHEMBL6853 Ki = 68.3 nM 7.17
CHEMBL6633 Ki = 70.1 nM 7.15
CHEMBL287117 Ki = 72.4 nM 7.14
CHEMBL7087 Ki = 73.0 nM 7.14
CHEMBL6724 Ki = 75.7 nM 7.12
CHEMBL77517 INDISULAM Ki = 84.1 nM 7.08
CHEMBL266240 Ki = 87.3 nM 7.06
CHEMBL265674 Ki = 137.0 nM 6.86
CHEMBL750 ZONISAMIDE Ki = 140.0 nM 6.85
CHEMBL6685 Ki = 162.0 nM 6.79
CHEMBL419 MAFENIDE Ki = 350.0 nM 6.46
CHEMBL6753 Ki = 433.0 nM 6.36
CHEMBL35118 Ki = 493.0 nM 6.31
CHEMBL6852 Ki = 652.0 nM 6.19
CHEMBL6919 Ki = 695.0 nM 6.16
CHEMBL6705 Ki = 707.0 nM 6.15
CHEMBL21 SULFANILAMIDE Ki = 803.0 nM 6.09
CHEMBL7204 Ki = 848.0 nM 6.07
CHEMBL310671 SACCHARIN Ki = 876.0 nM 6.06