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Compound Detail

CHEMBL2024627

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C=CCCOC(=O)[C@@]1(C)CC[C@]2(C)CC[C@]3(C)C(=CC(=O)[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1

Basic Information

ChEMBL ID CHEMBL2024627
Phase Preclinical
Structure Type MOL
InChI Key LBJFMELQLNDMGE-JYVVQSDUSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

524.8
MW (Da)
7.45
ALogP
4
HBA
1
HBD
63.6
PSA (Ų)
0.24
QED
2
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H52O4
MW 524.79
Aromatic Rings 0
Heavy Atoms 38
NP-Likeness 2.83

Activity Summary

IC50 1 meas.
Ki 1 meas. best 4.83

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Acetylcholinesterase
CHEMBL4078
Ki 4.83 4.83 14870.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Acetylcholinesterase Ki = 14870.0 nM 4.83 Inhibition of Electrophorus electricus AChE using acetylthiocholine iodide as su... 24853320

Literature References

PubMed DOI Target Context # Activities
22520261 10.1016/j.bmcl.2012.03.081 Hepatitis B virus 3
22520261 10.1016/j.bmcl.2012.03.081 Unchecked 3
22520261 10.1016/j.bmcl.2012.03.081 ADMET 1
24853320 10.1016/j.bmc.2014.04.046 Acetylcholinesterase 1
24853320 10.1016/j.bmc.2014.04.046 Cholinesterase 1
24853320 10.1016/j.bmc.2014.04.046 Unchecked 1

Data from ChEMBL 36 via Core Engine