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

CHEMBL4847532

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
O=S(=O)(c1ccccc1)n1ccc2c(OCCNCCNCc3cccc(Cl)c3)cccc21

Basic Information

ChEMBL ID CHEMBL4847532
Phase Preclinical
Structure Type MOL
InChI Key OQHRGQKGSVATEK-UHFFFAOYSA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

484.0
MW (Da)
4.29
ALogP
6
HBA
2
HBD
72.4
PSA (Ų)
0.31
QED
0
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H26ClN3O3S
MW 484.02
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.29

Activity Summary

IC50 2 meas. best 5.97
Ki 1 meas. best 8.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.7 8.7 2.0 1
Cholinesterase
CHEMBL5763
IC50 5.97 5.97 1075.0 1
Acetylcholinesterase
CHEMBL4078
IC50 5.32 5.32 4841.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34461507 10.1016/j.ejmech.2021.113783 Amyloid-beta precursor protein 2
34461507 10.1016/j.ejmech.2021.113783 5-hydroxytryptamine receptor 6 1
34461507 10.1016/j.ejmech.2021.113783 Cholinesterase 1
34461507 10.1016/j.ejmech.2021.113783 Acetylcholinesterase 1
34461507 10.1016/j.ejmech.2021.113783 Unchecked 1

Data from ChEMBL 36 via Core Engine