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Assay Detail

CHEMBL5115053

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

Binding
Inhibition of human carbonic anhydrase 1 assessed as inhibition constant incubated for 15 mins prior to testing by phenol red based stopped-flow CO2 hydration assay
15
Total Activities
15
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

Development of 4-((3-oxo-3-phenylpropyl)amino)benzenesulfonamide derivatives utilizing tail/dual-tail approaches as novel carbonic anhydrase inhibitors.
Elbadawi MM, Eldehna WM, Nocentini A, Somaa WR, Al-Rashood ST, Elkaeed EB, El Hassab MA, Abdel-Aziz HA, Supuran CT, Fares M.
Eur J Med Chem (2022) 238 : 114412 -114412
PubMed 35551035 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 15 6.42 7.31

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5203184 1 7.31
CHEMBL5183126 1 7.10
CHEMBL5192106 1 7.09
CHEMBL5201519 1 7.00
CHEMBL5179294 1 6.78
CHEMBL20 ACETAZOLAMIDE 4.0 1 6.60
CHEMBL5190695 1 6.54
CHEMBL5170382 1 6.53
CHEMBL5204971 1 6.48
CHEMBL5203094 1 6.39
CHEMBL5195261 1 6.24
CHEMBL5194070 1 6.04
CHEMBL5188494 1 5.77
CHEMBL1615281 SLC-0111 1.0 1 5.29
CHEMBL5193206 1 5.19

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5203184 Ki = 49.3 nM 7.31
CHEMBL5183126 Ki = 79.5 nM 7.10
CHEMBL5192106 Ki = 81.9 nM 7.09
CHEMBL5201519 Ki = 98.9 nM 7.00
CHEMBL5179294 Ki = 165.7 nM 6.78
CHEMBL20 ACETAZOLAMIDE Ki = 250.0 nM 6.60
CHEMBL5190695 Ki = 289.1 nM 6.54
CHEMBL5170382 Ki = 298.2 nM 6.53
CHEMBL5204971 Ki = 331.4 nM 6.48
CHEMBL5203094 Ki = 403.8 nM 6.39
CHEMBL5195261 Ki = 575.2 nM 6.24
CHEMBL5194070 Ki = 907.3 nM 6.04
CHEMBL5188494 Ki = 1711.0 nM 5.77
CHEMBL1615281 SLC-0111 Ki = 5080.0 nM 5.29
CHEMBL5193206 Ki = 6459.0 nM 5.19