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Assay Detail

CHEMBL4369236

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

Binding
Inhibition of human carbonic anhydrase-9 incubated for 15 mins prior to testing by stopped-flow CO2 hydration assay
16
Total Activities
16
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 9 (CHEMBL3594)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Novel benzoyl thioureido benzene sulfonamides as highly potent and selective inhibitors of carbonic anhydrase IX: optimization and bioactive studies.
Liu L, Wang W, Huang J, Zhao Z, Li H, Xu Y.
Medchemcomm (2018) 9 : 2100 -2105
PubMed 30746068 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 8.47 9.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL179559 1 9.92
CHEMBL18 ETHOXZOLAMIDE 4.0 1 9.60
CHEMBL4473329 1 9.52
CHEMBL1370332 1 9.33
CHEMBL2298035 1 9.32
CHEMBL2392423 1 8.54
CHEMBL3290513 1 8.47
CHEMBL2298033 1 8.38
CHEMBL3237495 1 8.36
CHEMBL20 ACETAZOLAMIDE 4.0 1 8.11
CHEMBL3237492 1 7.72
CHEMBL4538894 1 7.59
CHEMBL4584443 1 7.59
CHEMBL3237494 1 7.37
CHEMBL4456875 1 7.26
CHEMBL4447505 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL179559 IC50 = 0.12 nM 9.92
CHEMBL18 ETHOXZOLAMIDE IC50 = 0.25 nM 9.60
CHEMBL4473329 IC50 = 0.3 nM 9.52
CHEMBL1370332 IC50 = 0.47 nM 9.33
CHEMBL2298035 IC50 = 0.48 nM 9.32
CHEMBL2392423 IC50 = 2.86 nM 8.54
CHEMBL3290513 IC50 = 3.42 nM 8.47
CHEMBL2298033 IC50 = 4.14 nM 8.38
CHEMBL3237495 IC50 = 4.42 nM 8.36
CHEMBL20 ACETAZOLAMIDE IC50 = 7.72 nM 8.11
CHEMBL3237492 IC50 = 18.98 nM 7.72
CHEMBL4538894 IC50 = 25.5 nM 7.59
CHEMBL4584443 IC50 = 25.75 nM 7.59
CHEMBL3237494 IC50 = 42.23 nM 7.37
CHEMBL4456875 IC50 = 54.35 nM 7.26
CHEMBL4447505 IC50 > 104.0 nM -