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

CHEMBL328165

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
CCCCC1OP(=O)(OCC2C=CC(n3cc(C)c(=O)[nH]c3=O)O2)Oc2cccc(Cl)c21

Basic Information

ChEMBL ID CHEMBL328165
Phase Preclinical
Structure Type MOL
InChI Key JGMQXPSFUSTZBV-UHFFFAOYSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

482.9
MW (Da)
4.42
ALogP
8
HBA
1
HBD
108.8
PSA (Ų)
0.46
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H24ClN2O7P
MW 482.86
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness 0.35

Activity Summary

EC50 1 meas. best 6.72
IC50 1 meas. best 4.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
CCRF-CEM
CHEMBL382
EC50 6.72 6.72 190.0 1
Cholinesterase
CHEMBL1914
IC50 4.89 4.89 13000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
CCRF-CEM EC50 = 190.0 nM 6.72 Anti-HIV-1 activity tested in human lymphocytic CEM cells 15139762
Cholinesterase IC50 = 13000.0 nM 4.89 Inhibitory activity towards human butyrylcholinesterase 15139762

Literature References

PubMed DOI Target Context # Activities
15139762 10.1021/jm031032a Acetylcholinesterase 1
15139762 10.1021/jm031032a Cholinesterase 1
15139762 10.1021/jm031032a CCRF-CEM 1

Data from ChEMBL 36 via Core Engine