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Assay Detail

CHEMBL3372049

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

Binding
Inhibition of recombinant human carbonic anhydrase 2 after 15 mins by stopped flow CO2 hydration 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

Selective inhibition of human carbonic anhydrases by novel amide derivatives of probenecid: synthesis, biological evaluation and molecular modelling studies.
D'Ascenzio M, Carradori S, Secci D, Vullo D, Ceruso M, Akdemir A, Supuran CT.
Bioorg Med Chem (2014) 22 : 3982 -3988
PubMed 25027802 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 14 7.15 7.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.92
CHEMBL897 PROBENECID 4.0 1 6.37
CHEMBL3311028 1 -
CHEMBL3311027 1 -
CHEMBL3311026 1 -
CHEMBL3311025 1 -
CHEMBL3311024 1 -
CHEMBL3311023 1 -
CHEMBL3310916 1 -
CHEMBL3310915 1 -
CHEMBL3310914 1 -
CHEMBL3310913 1 -
CHEMBL3310912 1 -
CHEMBL3310911 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL20 ACETAZOLAMIDE Ki = 12.0 nM 7.92
CHEMBL897 PROBENECID Ki = 431.0 nM 6.37
CHEMBL3311028 Ki > 10000.0 nM -
CHEMBL3311027 Ki > 10000.0 nM -
CHEMBL3311026 Ki > 10000.0 nM -
CHEMBL3311025 Ki > 10000.0 nM -
CHEMBL3311024 Ki > 10000.0 nM -
CHEMBL3311023 Ki > 10000.0 nM -
CHEMBL3310916 Ki > 10000.0 nM -
CHEMBL3310915 Ki > 10000.0 nM -
CHEMBL3310914 Ki > 10000.0 nM -
CHEMBL3310913 Ki > 10000.0 nM -
CHEMBL3310912 Ki > 10000.0 nM -
CHEMBL3310911 Ki > 10000.0 nM -