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Assay Detail

CHEMBL5536444

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

Binding
Inhibition of recombinant human CA1 incubated for 15 mins by phenol red dye based 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 1 (CHEMBL261)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Novel 2,4-Dichloro-5-sulfamoylbenzoic Acid Oxime Esters: First Studies as Potential Human Carbonic Anhydrase Inhibitors.
Kilbile JT, Sapkal SB, Renzi G, D'Agostino I, Cutarella L, Mori M, De Filippis B, Islam I, Massardi ML, Somenza E, Ronca R, Tamboli Y, Carta F, Supuran CT.
ACS Med Chem Lett (2024) 15 : 972 -978
PubMed 38894925 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 16 7.60 9.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL120886 1 9.28
CHEMBL5574542 1 9.03
CHEMBL5569372 1 8.43
CHEMBL5570465 1 8.28
CHEMBL5572726 1 8.17
CHEMBL5563676 1 8.09
CHEMBL5570722 1 7.67
CHEMBL5566655 1 7.53
CHEMBL5589893 1 7.44
CHEMBL5562673 1 7.35
CHEMBL5555149 1 7.16
CHEMBL5573950 1 7.07
CHEMBL20 ACETAZOLAMIDE 4.0 1 6.60
CHEMBL5594498 1 6.59
CHEMBL5564949 1 6.58
CHEMBL5575026 1 6.35

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL120886 Ki = 0.52 nM 9.28
CHEMBL5574542 Ki = 0.93 nM 9.03
CHEMBL5569372 Ki = 3.7 nM 8.43
CHEMBL5570465 Ki = 5.3 nM 8.28
CHEMBL5572726 Ki = 6.7 nM 8.17
CHEMBL5563676 Ki = 8.2 nM 8.09
CHEMBL5570722 Ki = 21.3 nM 7.67
CHEMBL5566655 Ki = 29.5 nM 7.53
CHEMBL5589893 Ki = 36.5 nM 7.44
CHEMBL5562673 Ki = 44.6 nM 7.35
CHEMBL5555149 Ki = 69.5 nM 7.16
CHEMBL5573950 Ki = 84.4 nM 7.07
CHEMBL20 ACETAZOLAMIDE Ki = 250.0 nM 6.60
CHEMBL5594498 Ki = 255.0 nM 6.59
CHEMBL5564949 Ki = 263.0 nM 6.58
CHEMBL5575026 Ki = 445.0 nM 6.35