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Assay Detail

CHEMBL656566

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

Binding
50% inhibitory concentration against human carbonic anhydrase II (HCA II) after pre-incubation at 3 degree C
15
Total Activities
15
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
IC50 15 8.00 8.44

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1788291 1 8.44
CHEMBL417975 SEZOLAMIDE 2.0 1 8.40
CHEMBL2092886 1 8.34
CHEMBL314569 1 8.28
CHEMBL1204135 SEZOLAMIDE HYDROCHLORIDE -1.0 1 8.23
CHEMBL1788205 1 8.17
CHEMBL545239 1 8.14
CHEMBL543604 1 8.04
CHEMBL554091 1 8.04
CHEMBL20 ACETAZOLAMIDE 4.0 1 8.00
CHEMBL554854 1 7.91
CHEMBL545245 1 7.86
CHEMBL2092885 1 7.69
CHEMBL2092887 1 7.28
CHEMBL555182 1 7.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1788291 IC50 = 3.6 nM 8.44
CHEMBL417975 SEZOLAMIDE IC50 = 4.0 nM 8.40
CHEMBL2092886 IC50 = 4.6 nM 8.34
CHEMBL314569 IC50 = 5.3 nM 8.28
CHEMBL1204135 SEZOLAMIDE HYDROCHLORIDE IC50 = 5.9 nM 8.23
CHEMBL1788205 IC50 = 6.7 nM 8.17
CHEMBL545239 IC50 = 7.3 nM 8.14
CHEMBL543604 IC50 = 9.2 nM 8.04
CHEMBL554091 IC50 = 9.2 nM 8.04
CHEMBL20 ACETAZOLAMIDE IC50 = 9.9 nM 8.00
CHEMBL554854 IC50 = 12.4 nM 7.91
CHEMBL545245 IC50 = 13.9 nM 7.86
CHEMBL2092885 IC50 = 20.6 nM 7.69
CHEMBL2092887 IC50 = 53.1 nM 7.28
CHEMBL555182 IC50 = 70.0 nM 7.16