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Assay Detail

CHEMBL657823

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

Binding
Inhibition of human cloned Carbonic anhydrase I (hCA I,cytosolic form)
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

Carbonic anhydrase 1 (CHEMBL261)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Carbonic anhydrase inhibitors. Synthesis of water-soluble, topically effective, intraocular pressure-lowering aromatic/heterocyclic sulfonamides containing cationic or anionic moieties: is the tail more important than the ring?
Scozzafava A, Menabuoni L, Mincione F, Briganti F, Mincione G, Supuran CT.
J Med Chem (1999) 42 : 2641 -2650
PubMed 10411484 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 12 6.40 7.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL420610 1 7.92
CHEMBL90382 1 7.75
CHEMBL88232 1 7.41
CHEMBL6685 1 7.26
CHEMBL35118 1 7.16
CHEMBL13646 1 6.34
CHEMBL432818 1 6.30
CHEMBL88519 1 6.22
CHEMBL90218 1 6.22
CHEMBL330346 1 4.81
CHEMBL327669 1 4.70
CHEMBL86751 1 4.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL420610 Ki = 12.0 nM 7.92
CHEMBL90382 Ki = 18.0 nM 7.75
CHEMBL88232 Ki = 39.0 nM 7.41
CHEMBL6685 Ki = 55.0 nM 7.26
CHEMBL35118 Ki = 70.0 nM 7.16
CHEMBL13646 Ki = 455.0 nM 6.34
CHEMBL432818 Ki = 500.0 nM 6.30
CHEMBL88519 Ki = 600.0 nM 6.22
CHEMBL90218 Ki = 600.0 nM 6.22
CHEMBL330346 Ki = 15500.0 nM 4.81
CHEMBL327669 Ki = 20000.0 nM 4.70
CHEMBL86751 Ki = 20000.0 nM 4.70