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Compound Detail

CHEMBL559822

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C[N+]1(CCNC(=O)c2cnc3c4c(cccc24)-c2ccccc2C3=O)CCOCC1.[I-]

Basic Information

ChEMBL ID CHEMBL559822
Phase Preclinical
Structure Type MOL
InChI Key YPZOTGNAGRWQOJ-UHFFFAOYSA-N
Parent Compound CHEMBL1197115
Active Moiety CHEMBL1197115
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

402.5
MW (Da)
2.65
ALogP
4
HBA
1
HBD
68.3
PSA (Ų)
0.53
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H24IN3O3
MW 529.38
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -0.25

Activity Summary

IC50 2 meas. best 5.91

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Acetylcholinesterase
CHEMBL4078
IC50 5.91 5.91 1240.0 1
Cholinesterase
CHEMBL5763
IC50 4.93 4.93 11690.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Acetylcholinesterase IC50 = 1240.0 nM 5.91 Inhibition of electric eel AChE by Ellman's method 19243862
Cholinesterase IC50 = 11690.0 nM 4.93 Inhibition of equine serum BuChE by Ellman's method 19243862

Literature References

PubMed DOI Target Context # Activities
19243862 10.1016/j.ejmech.2009.01.021 Unchecked 1
19243862 10.1016/j.ejmech.2009.01.021 Cholinesterase 1
19243862 10.1016/j.ejmech.2009.01.021 Acetylcholinesterase 1

Data from ChEMBL 36 via Core Engine