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Assay Detail

CHEMBL1106334

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

Binding
Inhibition of human recombinant carbonic anhydrase 2 after 15 mins by stopped flow carbon dioxide hydrase assay method
10
Total Activities
10
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

Inhibition studies of a beta-carbonic anhydrase from Brucella suis with a series of water soluble glycosyl sulfanilamides.
Vullo D, Nishimori I, Scozzafava A, Köhler S, Winum JY, Supuran CT.
Bioorg Med Chem Lett (2010) 20 : 2178 -2182
PubMed 20211561 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 10 7.69 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1093178 1 8.00
CHEMBL1089637 1 7.92
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.92
CHEMBL1090524 1 7.85
CHEMBL1092670 1 7.82
CHEMBL1089967 1 7.80
CHEMBL1090522 1 7.75
CHEMBL1089968 1 7.64
CHEMBL1090523 1 7.60
CHEMBL21 SULFANILAMIDE 4.0 1 6.62

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1093178 Ki = 10.0 nM 8.00
CHEMBL1089637 Ki = 12.0 nM 7.92
CHEMBL20 ACETAZOLAMIDE Ki = 12.0 nM 7.92
CHEMBL1090524 Ki = 14.0 nM 7.85
CHEMBL1092670 Ki = 15.0 nM 7.82
CHEMBL1089967 Ki = 16.0 nM 7.80
CHEMBL1090522 Ki = 18.0 nM 7.75
CHEMBL1089968 Ki = 23.0 nM 7.64
CHEMBL1090523 Ki = 25.0 nM 7.60
CHEMBL21 SULFANILAMIDE Ki = 240.0 nM 6.62