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

CHEMBL1816746

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

Binding
Inhibition of human ERG expressed in CHO cells by high throughput single cell planar patch clamp method
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Publication

Synthesis and pharmacological characterization of bicyclic triple reuptake inhibitor 3-aryl octahydrocyclopenta[c]pyrrole analogues.
Shao L, Hewitt MC, Malcolm SC, Wang F, Ma J, Campbell UC, Spicer NA, Engel SR, Hardy LW, Jiang ZD, Schreiber R, Spear KL, Varney MA.
J Med Chem (2011) 54 : 5283 -5295
PubMed 21739935 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 5.33 5.63

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1813315 1 5.63
CHEMBL1813472 1 5.44
CHEMBL1813314 1 5.38
CHEMBL1813317 1 5.36
CHEMBL1813316 1 5.33
CHEMBL1813475 1 5.28
CHEMBL1813484 1 5.26
CHEMBL1813478 1 5.25
CHEMBL1813474 1 5.19
CHEMBL1813471 1 5.19
CHEMBL1813485 1 -
CHEMBL1813483 1 -
CHEMBL1813477 1 -
CHEMBL1813476 1 -
CHEMBL1813489 1 -
CHEMBL1813487 1 -
CHEMBL1813470 1 -
CHEMBL1813313 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1813315 IC50 = 2320.0 nM 5.63
CHEMBL1813472 IC50 = 3640.0 nM 5.44
CHEMBL1813314 IC50 = 4140.0 nM 5.38
CHEMBL1813317 IC50 = 4330.0 nM 5.36
CHEMBL1813316 IC50 = 4730.0 nM 5.33
CHEMBL1813475 IC50 = 5280.0 nM 5.28
CHEMBL1813484 IC50 = 5430.0 nM 5.26
CHEMBL1813478 IC50 = 5640.0 nM 5.25
CHEMBL1813474 IC50 = 6400.0 nM 5.19
CHEMBL1813471 IC50 = 6480.0 nM 5.19
CHEMBL1813485 IC50 - -
CHEMBL1813483 IC50 - -
CHEMBL1813477 IC50 - -
CHEMBL1813476 IC50 - -
CHEMBL1813489 IC50 - -
CHEMBL1813487 IC50 - -
CHEMBL1813470 IC50 - -
CHEMBL1813313 IC50 - -