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Assay Detail

CHEMBL658943

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Binding
The equilibrium dissociation constant of the inhibitor-enzyme complex of human Carbonic anhydrase II
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Carbonic anhydrase 2 (CHEMBL205)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma.
Baldwin JJ, Ponticello GS, Anderson PS, Christy ME, Murcko MA, Randall WC, Schwam H, Sugrue MF, Springer JP, Gautheron P.
J Med Chem (1989) 32 : 2510 -2513
PubMed 2585439 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 9 8.61 9.16

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL545239 1 9.16
CHEMBL1204135 SEZOLAMIDE HYDROCHLORIDE -1.0 1 9.15
CHEMBL543604 1 8.96
CHEMBL554854 1 8.74
CHEMBL545245 1 8.64
CHEMBL554091 1 8.43
CHEMBL2092886 1 8.21
CHEMBL314569 1 8.17
CHEMBL555182 1 8.03

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL545239 Ki = 0.69 nM 9.16
CHEMBL1204135 SEZOLAMIDE HYDROCHLORIDE Ki = 0.7 nM 9.15
CHEMBL543604 Ki = 1.1 nM 8.96
CHEMBL554854 Ki = 1.8 nM 8.74
CHEMBL545245 Ki = 2.3 nM 8.64
CHEMBL554091 Ki = 3.7 nM 8.43
CHEMBL2092886 Ki = 6.2 nM 8.21
CHEMBL314569 Ki = 6.8 nM 8.17
CHEMBL555182 Ki = 9.3 nM 8.03