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Compound Detail

CHEMBL2059305

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O=C1CCc2ccccc2N1CCCN1CCC(c2ccc3[nH]ccc3c2)CC1

Basic Information

ChEMBL ID CHEMBL2059305
Phase Preclinical
Structure Type MOL
InChI Key QJMDUKSLBFAKOC-UHFFFAOYSA-N
3
Targets
3
Activities
3
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

387.5
MW (Da)
4.72
ALogP
2
HBA
1
HBD
39.3
PSA (Ų)
0.69
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H29N3O
MW 387.53
Aromatic Rings 3
Heavy Atoms 29
NP-Likeness -0.91

Activity Summary

EC50 1 meas. best 6.8
IC50 1 meas. best 5.36
Ki 1 meas. best 7.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
D(2) dopamine receptor
CHEMBL217
Ki 7.38 7.38 42.0 1
Muscarinic acetylcholine receptor M1
CHEMBL216
EC50 6.8 6.8 160.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.36 5.36 4400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22677319 10.1016/j.bmcl.2012.05.048 No relevant target 2
22677319 10.1016/j.bmcl.2012.05.048 Muscarinic acetylcholine receptor M1 2
22677319 10.1016/j.bmcl.2012.05.048 Voltage-gated inwardly rectifying potassium channel KCNH2 1
22677319 10.1016/j.bmcl.2012.05.048 Liver microsomes 1
22677319 10.1016/j.bmcl.2012.05.048 D(2) dopamine receptor 1

Data from ChEMBL 36 via Core Engine