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Assay Detail

CHEMBL1177459

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

Binding
Inhibition of human recombinant carbonic anhydrase 12 catalytic domain preincubated for 15 mins by CO2 hydration method
6
Total Activities
6
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 12 (CHEMBL3242)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Coumarinyl-substituted sulfonamides strongly inhibit several human carbonic anhydrase isoforms: solution and crystallographic investigations.
Wagner J, Avvaru BS, Robbins AH, Scozzafava A, Supuran CT, McKenna R.
Bioorg Med Chem (2010) 18 : 4873 -4878
PubMed 20598552 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 7.55 8.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL20 ACETAZOLAMIDE 4.0 1 8.60
CHEMBL489182 1 8.22
CHEMBL492022 1 7.26
CHEMBL477822 1 7.20
CHEMBL478669 1 7.11
CHEMBL514556 1 6.89

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL20 ACETAZOLAMIDE Ki = 2.5 nM 8.60
CHEMBL489182 Ki = 6.0 nM 8.22
CHEMBL492022 Ki = 55.0 nM 7.26
CHEMBL477822 Ki = 63.0 nM 7.20
CHEMBL478669 Ki = 78.0 nM 7.11
CHEMBL514556 Ki = 128.0 nM 6.89