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Assay Detail

CHEMBL4813795

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

Binding
Inhibition of recombinant human CA7 incubated for 15 mins by phenol red dye based stopped flow CO2 hydration assay
17
Total Activities
17
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 7 (CHEMBL2326)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis and biochemical evaluation of novel carbonic anhydrase inhibitors triggered by structural knowledge on hCA VII.
Mancuso F, Di Fiore A, De Luca L, Angeli A, De Simone G, Supuran CT, Gitto R.
Bioorg Med Chem (2021) 44 : 116279 -116279
PubMed 34216985 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 7.85 9.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL220492 TOPIRAMATE 4.0 1 9.05
CHEMBL20 ACETAZOLAMIDE 4.0 1 8.60
CHEMBL4632436 1 8.54
CHEMBL4876892 1 8.37
CHEMBL4873540 1 8.15
CHEMBL4875463 1 8.14
CHEMBL4852567 1 8.12
CHEMBL4863183 1 8.08
CHEMBL4876588 1 8.03
CHEMBL4856098 1 7.81
CHEMBL4864679 1 7.67
CHEMBL4862904 1 7.25
CHEMBL4869644 1 7.24
CHEMBL4878898 1 7.17
CHEMBL4643115 1 7.15
CHEMBL4869570 1 7.08
CHEMBL4855985 1 7.08

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL220492 TOPIRAMATE Ki = 0.9 nM 9.05
CHEMBL20 ACETAZOLAMIDE Ki = 2.5 nM 8.60
CHEMBL4632436 Ki = 2.9 nM 8.54
CHEMBL4876892 Ki = 4.3 nM 8.37
CHEMBL4873540 Ki = 7.1 nM 8.15
CHEMBL4875463 Ki = 7.2 nM 8.14
CHEMBL4852567 Ki = 7.6 nM 8.12
CHEMBL4863183 Ki = 8.3 nM 8.08
CHEMBL4876588 Ki = 9.4 nM 8.03
CHEMBL4856098 Ki = 15.5 nM 7.81
CHEMBL4864679 Ki = 21.5 nM 7.67
CHEMBL4862904 Ki = 56.4 nM 7.25
CHEMBL4869644 Ki = 57.9 nM 7.24
CHEMBL4878898 Ki = 68.3 nM 7.17
CHEMBL4643115 Ki = 70.7 nM 7.15
CHEMBL4869570 Ki = 84.0 nM 7.08
CHEMBL4855985 Ki = 82.5 nM 7.08