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Assay Detail

CHEMBL5225827

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

Binding
Inhibition of human carbonic anhydrase 2 assessed as inhibition constant by stopped-flow CO2 hydration assay
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

Structural Characterization of Thiadiazolesulfonamide Inhibitors Bound to <i>Neisseria gonorrhoeae</i> α-Carbonic Anhydrase.
Marapaka AK, Nocentini A, Youse MS, An W, Holly KJ, Das C, Yadav R, Seleem MN, Supuran CT, Flaherty DP.
ACS Med Chem Lett (2023) 14 : 103 -109
PubMed 36655133 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 10 7.74 9.49

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4782535 1 9.49
CHEMBL4741159 1 8.09
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.90
CHEMBL4739913 1 7.70
CHEMBL4750765 1 7.61
CHEMBL281376 1 7.54
CHEMBL5280695 1 7.42
CHEMBL4749585 1 7.33
CHEMBL265674 1 7.22
CHEMBL4753745 1 7.11

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4782535 Ki = 0.32 nM 9.49
CHEMBL4741159 Ki = 8.1 nM 8.09
CHEMBL20 ACETAZOLAMIDE Ki = 12.5 nM 7.90
CHEMBL4739913 Ki = 20.2 nM 7.70
CHEMBL4750765 Ki = 24.5 nM 7.61
CHEMBL281376 Ki = 29.0 nM 7.54
CHEMBL5280695 Ki = 38.3 nM 7.42
CHEMBL4749585 Ki = 47.2 nM 7.33
CHEMBL265674 Ki = 60.0 nM 7.22
CHEMBL4753745 Ki = 78.4 nM 7.11