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Assay Detail

CHEMBL1010057

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

Binding
Inhibition of human recombinant CA2 by stopped-flow CO2 hydrase assay
9
Total Activities
9
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

Dual inhibitors of matrix metalloproteinases and carbonic anhydrases: iminodiacetyl-based hydroxamate-benzenesulfonamide conjugates.
Marques SM, Nuti E, Rossello A, Supuran CT, Tuccinardi T, Martinelli A, Santos MA.
J Med Chem (2008) 51 : 7968 -7979
PubMed 19053764 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 9 7.76 8.38

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL471537 1 8.38
CHEMBL51668 1 8.30
CHEMBL388671 1 8.08
CHEMBL388453 1 8.03
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.92
CHEMBL234735 1 7.46
CHEMBL234529 1 7.24
CHEMBL234737 1 7.20
CHEMBL234530 1 7.19

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL471537 Ki = 4.2 nM 8.38
CHEMBL51668 Ki = 5.0 nM 8.30
CHEMBL388671 Ki = 8.4 nM 8.08
CHEMBL388453 Ki = 9.3 nM 8.03
CHEMBL20 ACETAZOLAMIDE Ki = 12.0 nM 7.92
CHEMBL234735 Ki = 35.0 nM 7.46
CHEMBL234529 Ki = 57.0 nM 7.24
CHEMBL234737 Ki = 63.0 nM 7.20
CHEMBL234530 Ki = 65.0 nM 7.19