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Assay Detail

CHEMBL3607052

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Binding
Inhibition of Nostoc commune gamma carbonic anhydrase by CO2 hydration assay
39
Total Activities
39
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Nostoc commune
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Pseudoalteromonas haloplanktis.
Vullo D, De Luca V, Del Prete S, Carginale V, Scozzafava A, Capasso C, Supuran CT.
Bioorg Med Chem Lett (2015) 25 : 3550 -3555
PubMed 26174556 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 39 6.52 7.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL266026 1 7.39
CHEMBL73962 BENZOLAMIDE 1 7.31
CHEMBL865 VALDECOXIB 4.0 1 7.28
CHEMBL435 HYDROCHLOROTHIAZIDE 4.0 1 7.23
CHEMBL26 SULPIRIDE 3.0 1 7.22
CHEMBL268439 1 7.18
CHEMBL220492 TOPIRAMATE 4.0 1 7.18
CHEMBL218490 DORZOLAMIDE 4.0 1 7.17
CHEMBL414 CARZENIDE 2.0 1 7.13
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.12
CHEMBL6633 1 7.11
CHEMBL220491 BRINZOLAMIDE 4.0 1 7.09
CHEMBL328560 SULTHIAME 3.0 1 7.08
CHEMBL750 ZONISAMIDE 4.0 1 7.07
CHEMBL265674 1 7.07
CHEMBL118 CELECOXIB 4.0 1 7.06
CHEMBL77517 INDISULAM 2.0 1 7.04
CHEMBL19 METHAZOLAMIDE 4.0 1 6.72
CHEMBL18 ETHOXZOLAMIDE 4.0 1 6.58
CHEMBL266240 1 6.57
CHEMBL17 DICHLORPHENAMIDE 4.0 1 6.46
CHEMBL2324864 1 6.40
CHEMBL310671 SACCHARIN 3.0 1 6.39
CHEMBL6753 1 6.32
CHEMBL21 SULFANILAMIDE 4.0 1 6.31
CHEMBL6852 1 6.31
CHEMBL269122 1 6.26
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 6.20
CHEMBL2324868 1 6.17
CHEMBL7087 1 6.13

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL266026 Ki = 40.3 nM 7.39
CHEMBL73962 BENZOLAMIDE Ki = 48.5 nM 7.31
CHEMBL865 VALDECOXIB Ki = 53.1 nM 7.28
CHEMBL435 HYDROCHLOROTHIAZIDE Ki = 58.7 nM 7.23
CHEMBL26 SULPIRIDE Ki = 60.5 nM 7.22
CHEMBL268439 Ki = 66.7 nM 7.18
CHEMBL220492 TOPIRAMATE Ki = 65.7 nM 7.18
CHEMBL218490 DORZOLAMIDE Ki = 67.4 nM 7.17
CHEMBL414 CARZENIDE Ki = 74.6 nM 7.13
CHEMBL20 ACETAZOLAMIDE Ki = 75.8 nM 7.12
CHEMBL6633 Ki = 78.3 nM 7.11
CHEMBL220491 BRINZOLAMIDE Ki = 81.3 nM 7.09
CHEMBL328560 SULTHIAME Ki = 82.4 nM 7.08
CHEMBL750 ZONISAMIDE Ki = 85.6 nM 7.07
CHEMBL265674 Ki = 84.7 nM 7.07
CHEMBL118 CELECOXIB Ki = 87.6 nM 7.06
CHEMBL77517 INDISULAM Ki = 92.3 nM 7.04
CHEMBL19 METHAZOLAMIDE Ki = 191.0 nM 6.72
CHEMBL18 ETHOXZOLAMIDE Ki = 264.0 nM 6.58
CHEMBL266240 Ki = 269.0 nM 6.57
CHEMBL17 DICHLORPHENAMIDE Ki = 345.0 nM 6.46
CHEMBL2324864 Ki = 402.0 nM 6.40
CHEMBL310671 SACCHARIN Ki = 408.0 nM 6.39
CHEMBL6753 Ki = 480.0 nM 6.32
CHEMBL21 SULFANILAMIDE Ki = 488.0 nM 6.31
CHEMBL6852 Ki = 492.0 nM 6.31
CHEMBL269122 Ki = 553.0 nM 6.26
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 632.0 nM 6.20
CHEMBL2324868 Ki = 683.0 nM 6.17
CHEMBL7087 Ki = 742.0 nM 6.13
CHEMBL6784 Ki = 777.0 nM 6.11
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 785.0 nM 6.11
CHEMBL419 MAFENIDE Ki = 825.0 nM 6.08
CHEMBL6724 Ki = 872.0 nM 6.06
CHEMBL2324869 Ki = 2810.0 nM 5.55
CHEMBL6919 Ki = 4034.0 nM 5.39
CHEMBL224292 Ki = 7570.0 nM 5.12
CHEMBL6853 Ki = 20600.0 nM 4.69
CHEMBL7092 Ki = 23750.0 nM 4.62