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

CHEMBL643099

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

Binding
In vitro inhibition of human placental aldose reductase.
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Aldo-keto reductase family 1 member B1 (CHEMBL1900)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A highly specific aldose reductase inhibitor, ethyl 1-benzyl-3-hydroxy-2(5H)-oxopyrrole-4-carboxylate, and its congeners.
Mylari BL, Beyer TA, Siegel TW.
J Med Chem (1991) 34 : 1011 -1018
PubMed 1900532 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 6.12 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL266773 1 6.70
CHEMBL7415 1 6.62
CHEMBL269550 1 6.58
CHEMBL7224 1 6.52
CHEMBL7183 1 6.51
CHEMBL6944 1 6.42
CHEMBL414208 1 6.39
CHEMBL6828 1 6.36
CHEMBL7603 1 6.30
CHEMBL269089 1 6.08
CHEMBL267651 1 5.92
CHEMBL7749 1 5.72
CHEMBL7658 1 5.64
CHEMBL266772 1 5.64
CHEMBL7461 1 5.60
CHEMBL7541 1 5.58
CHEMBL7304 1 5.48

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL266773 IC50 = 200.0 nM 6.70
CHEMBL7415 IC50 = 240.0 nM 6.62
CHEMBL269550 IC50 = 260.0 nM 6.58
CHEMBL7224 IC50 = 300.0 nM 6.52
CHEMBL7183 IC50 = 310.0 nM 6.51
CHEMBL6944 IC50 = 380.0 nM 6.42
CHEMBL414208 IC50 = 410.0 nM 6.39
CHEMBL6828 IC50 = 440.0 nM 6.36
CHEMBL7603 IC50 = 500.0 nM 6.30
CHEMBL269089 IC50 = 840.0 nM 6.08
CHEMBL267651 IC50 = 1200.0 nM 5.92
CHEMBL7749 IC50 = 1900.0 nM 5.72
CHEMBL7658 IC50 = 2300.0 nM 5.64
CHEMBL266772 IC50 = 2300.0 nM 5.64
CHEMBL7461 IC50 = 2500.0 nM 5.60
CHEMBL7541 IC50 = 2600.0 nM 5.58
CHEMBL7304 IC50 = 3300.0 nM 5.48