Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL1286651

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

Binding
Inhibition of Fischer-344 rat kidney AK1A1
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Aldo-keto reductase family 1 member A1 (CHEMBL3871)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

A diverse series of substituted benzenesulfonamides as aldose reductase inhibitors with antioxidant activity: design, synthesis, and in vitro activity.
Alexiou P, Demopoulos VJ.
J Med Chem (2010) 53 : 7756 -7766
PubMed 20936791 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 4.95 6.49

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1277476 1 6.49
CHEMBL1277203 1 5.16
CHEMBL1277477 1 5.01
CHEMBL507525 1 4.99
CHEMBL1277386 1 4.92
CHEMBL1277297 1 4.91
CHEMBL1277387 1 4.81
CHEMBL458568 1 4.71
CHEMBL458588 1 4.62
CHEMBL1277298 1 4.59
CHEMBL109 VALPROIC ACID 4.0 1 4.25
CHEMBL457486 1 -
CHEMBL1277113 1 -
CHEMBL1277202 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1277476 IC50 = 323.0 nM 6.49
CHEMBL1277203 IC50 = 6900.0 nM 5.16
CHEMBL1277477 IC50 = 9700.0 nM 5.01
CHEMBL507525 IC50 = 10300.0 nM 4.99
CHEMBL1277386 IC50 = 11900.0 nM 4.92
CHEMBL1277297 IC50 = 12400.0 nM 4.91
CHEMBL1277387 IC50 = 15420.0 nM 4.81
CHEMBL458568 IC50 = 19600.0 nM 4.71
CHEMBL458588 IC50 = 23800.0 nM 4.62
CHEMBL1277298 IC50 = 25500.0 nM 4.59
CHEMBL109 VALPROIC ACID IC50 = 56100.0 nM 4.25
CHEMBL457486 IC50 = 132900.0 nM -
CHEMBL1277113 IC50 = 105200.0 nM -
CHEMBL1277202 IC50 = 280700.0 nM -