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

CHEMBL492233

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=C(/C=C/c1ccccc1)O[C@@H]1CO[C@H]2[C@@H]1OC[C@@H]2OC(=O)NCc1ccccc1

Basic Information

ChEMBL ID CHEMBL492233
Phase Preclinical
Structure Type MOL
InChI Key FMGDUGJTFOCWHU-NIXJXNPBSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

409.4
MW (Da)
2.70
ALogP
6
HBA
1
HBD
83.1
PSA (Ų)
0.58
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H23NO6
MW 409.44
Aromatic Rings 2
Heavy Atoms 30
NP-Likeness 0.18

Activity Summary

IC50 2 meas. best 6.86

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cholinesterase
CHEMBL1914
IC50 6.86 6.86 137.0 1
Acetylcholinesterase
CHEMBL4078
IC50 4.25 4.25 55900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cholinesterase IC50 = 137.0 nM 6.86 Inhibition of human plasma BuchE by Ellman's method 18817366
Acetylcholinesterase IC50 = 55900.0 nM 4.25 Inhibition of electric eel AchE by Ellman's method 18817366

Literature References

PubMed DOI Target Context # Activities
18817366 10.1021/jm800564y Cholinesterase 2
18817366 10.1021/jm800564y Acetylcholinesterase 2
18817366 10.1021/jm800564y Unchecked 1

Data from ChEMBL 36 via Core Engine