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Assay Detail

CHEMBL1115565

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

Binding
Inhibition of human NET transfected in MDCK-Net6 cells
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type MDCK-Net6
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Sodium-dependent noradrenaline transporter (CHEMBL222)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Heterocyclic cycloalkanol ethylamines as norepinephrine reuptake inhibitors.
Sabatucci JP, Mahaney PE, Leiter J, Johnston G, Burroughs K, Cosmi S, Zhang Y, Ho D, Deecher DC, Trybulski E.
Bioorg Med Chem Lett (2010) 20 : 2809 -2812
PubMed 20378347 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 6.84 8.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL72 DESIPRAMINE 4.0 1 8.47
CHEMBL1175 DULOXETINE 4.0 1 8.40
CHEMBL1099179 1 7.52
CHEMBL1096495 1 7.25
CHEMBL1095850 1 7.24
CHEMBL1097148 1 7.02
CHEMBL1095525 1 7.00
CHEMBL1095523 1 6.65
CHEMBL1097469 1 6.59
CHEMBL637 VENLAFAXINE 4.0 1 6.27
CHEMBL1097470 1 6.26
CHEMBL1099212 1 6.24
CHEMBL1095524 1 6.14
CHEMBL1099178 1 4.75
CHEMBL1097146 1 -
CHEMBL1097147 1 -
CHEMBL1097660 1 -
CHEMBL1099134 1 -
CHEMBL1098855 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL72 DESIPRAMINE IC50 = 3.4 nM 8.47
CHEMBL1175 DULOXETINE IC50 = 4.0 nM 8.40
CHEMBL1099179 IC50 = 30.0 nM 7.52
CHEMBL1096495 IC50 = 56.0 nM 7.25
CHEMBL1095850 IC50 = 57.0 nM 7.24
CHEMBL1097148 IC50 = 95.0 nM 7.02
CHEMBL1095525 IC50 = 100.0 nM 7.00
CHEMBL1095523 IC50 = 225.0 nM 6.65
CHEMBL1097469 IC50 = 255.0 nM 6.59
CHEMBL637 VENLAFAXINE IC50 = 535.0 nM 6.27
CHEMBL1097470 IC50 = 550.0 nM 6.26
CHEMBL1099212 IC50 = 576.0 nM 6.24
CHEMBL1095524 IC50 = 720.0 nM 6.14
CHEMBL1099178 IC50 = 18000.0 nM 4.75
CHEMBL1097146 IC50 - -
CHEMBL1097147 IC50 - -
CHEMBL1097660 IC50 - -
CHEMBL1099134 IC50 - -
CHEMBL1098855 IC50 - -