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Assay Detail

CHEMBL3101212

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

Binding
Inhibition of Leishmania donovani chagasi recombinant beta-carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay
40
Total Activities
40
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Leishmania chagasi
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Sulfonamide inhibition studies of the δ-carbonic anhydrase from the diatom Thalassiosira weissflogii.
Vullo D, Del Prete S, Osman SM, De Luca V, Scozzafava A, Alothman Z, Supuran CT, Capasso C.
Bioorg Med Chem Lett (2014) 24 : 275 -279
PubMed 24314394 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 40 6.23 7.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL435 HYDROCHLOROTHIAZIDE 4.0 1 7.30
CHEMBL2324864 1 7.30
CHEMBL18 ETHOXZOLAMIDE 4.0 1 7.29
CHEMBL414 CARZENIDE 2.0 1 7.22
CHEMBL7146 1 7.13
CHEMBL266026 1 7.06
CHEMBL19 METHAZOLAMIDE 4.0 1 7.06
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.04
CHEMBL268439 1 7.02
CHEMBL269122 1 6.87
CHEMBL17 DICHLORPHENAMIDE 4.0 1 6.72
CHEMBL6784 1 6.64
CHEMBL73962 BENZOLAMIDE 1 6.63
CHEMBL77517 INDISULAM 2.0 1 6.50
CHEMBL865 VALDECOXIB 4.0 1 6.47
CHEMBL6919 1 6.41
CHEMBL6753 1 6.36
CHEMBL265674 1 6.23
CHEMBL118 CELECOXIB 4.0 1 6.15
CHEMBL220491 BRINZOLAMIDE 4.0 1 6.12
CHEMBL218490 DORZOLAMIDE 4.0 1 6.09
CHEMBL328560 SULTHIAME 3.0 1 6.08
CHEMBL224292 1 6.03
CHEMBL266240 1 5.32
CHEMBL6852 1 5.22
CHEMBL6724 1 5.08
CHEMBL2324868 1 5.05
CHEMBL2324869 1 5.04
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE 1 5.04
CHEMBL7092 1 5.04

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL435 HYDROCHLOROTHIAZIDE Ki = 50.2 nM 7.30
CHEMBL2324864 Ki = 50.2 nM 7.30
CHEMBL18 ETHOXZOLAMIDE Ki = 51.5 nM 7.29
CHEMBL414 CARZENIDE Ki = 59.6 nM 7.22
CHEMBL7146 Ki = 73.4 nM 7.13
CHEMBL266026 Ki = 87.1 nM 7.06
CHEMBL19 METHAZOLAMIDE Ki = 87.1 nM 7.06
CHEMBL20 ACETAZOLAMIDE Ki = 91.7 nM 7.04
CHEMBL268439 Ki = 95.1 nM 7.02
CHEMBL269122 Ki = 136.0 nM 6.87
CHEMBL17 DICHLORPHENAMIDE Ki = 189.0 nM 6.72
CHEMBL6784 Ki = 227.0 nM 6.64
CHEMBL73962 BENZOLAMIDE Ki = 236.0 nM 6.63
CHEMBL77517 INDISULAM Ki = 316.0 nM 6.50
CHEMBL865 VALDECOXIB Ki = 338.0 nM 6.47
CHEMBL6919 Ki = 389.0 nM 6.41
CHEMBL6753 Ki = 433.0 nM 6.36
CHEMBL265674 Ki = 584.0 nM 6.23
CHEMBL118 CELECOXIB Ki = 705.0 nM 6.15
CHEMBL220491 BRINZOLAMIDE Ki = 764.0 nM 6.12
CHEMBL218490 DORZOLAMIDE Ki = 806.0 nM 6.09
CHEMBL328560 SULTHIAME Ki = 834.0 nM 6.08
CHEMBL224292 Ki = 927.0 nM 6.03
CHEMBL266240 Ki = 4819.0 nM 5.32
CHEMBL6852 Ki = 5960.0 nM 5.22
CHEMBL6724 Ki = 8420.0 nM 5.08
CHEMBL2324868 Ki = 8910.0 nM 5.05
CHEMBL2324869 Ki = 9135.0 nM 5.04
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 9083.0 nM 5.04
CHEMBL7092 Ki = 9058.0 nM 5.04
CHEMBL21 SULFANILAMIDE Ki = 9251.0 nM 5.03
CHEMBL6853 Ki = 15600.0 nM 4.81
CHEMBL310671 SACCHARIN Ki > 100000.0 nM -
CHEMBL574 P-TOLUENESULFONAMIDE Ki > 100000.0 nM -
CHEMBL419 MAFENIDE Ki > 100000.0 nM -
CHEMBL7087 Ki > 100000.0 nM -
CHEMBL6633 Ki > 100000.0 nM -
CHEMBL220492 TOPIRAMATE Ki > 100000.0 nM -
CHEMBL750 ZONISAMIDE Ki > 100000.0 nM -
CHEMBL26 SULPIRIDE Ki > 100000.0 nM -