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Assay Detail

CHEMBL3588512

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

Binding
Inhibition of human carbonic anhydrase 2 by stopped-flow CO2 hydrase assay
14
Total Activities
14
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

New amide derivatives of Probenecid as selective inhibitors of carbonic anhydrase IX and XII: biological evaluation and molecular modelling studies.
Carradori S, Mollica A, Ceruso M, D'Ascenzio M, De Monte C, Chimenti P, Sabia R, Akdemir A, Supuran CT.
Bioorg Med Chem (2015) 23 : 2975 -2981
PubMed 26007302 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 14 6.49 6.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL20 ACETAZOLAMIDE 4.0 1 6.60
CHEMBL897 PROBENECID 4.0 1 6.37
CHEMBL3586211 1 -
CHEMBL3586212 1 -
CHEMBL3586213 1 -
CHEMBL3586214 1 -
CHEMBL3586215 1 -
CHEMBL3586216 1 -
CHEMBL3586217 1 -
CHEMBL3586218 1 -
CHEMBL3310916 1 -
CHEMBL3586219 1 -
CHEMBL3586220 1 -
CHEMBL3586221 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL20 ACETAZOLAMIDE Ki = 250.0 nM 6.60
CHEMBL897 PROBENECID Ki = 431.0 nM 6.37
CHEMBL3586211 Ki > 10000.0 nM -
CHEMBL3586212 Ki > 10000.0 nM -
CHEMBL3586213 Ki > 10000.0 nM -
CHEMBL3586214 Ki > 10000.0 nM -
CHEMBL3586215 Ki > 10000.0 nM -
CHEMBL3586216 Ki > 10000.0 nM -
CHEMBL3586217 Ki > 10000.0 nM -
CHEMBL3586218 Ki > 10000.0 nM -
CHEMBL3310916 Ki > 10000.0 nM -
CHEMBL3586219 Ki > 10000.0 nM -
CHEMBL3586220 Ki > 10000.0 nM -
CHEMBL3586221 Ki > 10000.0 nM -