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Compound Detail

CHEMBL1258312

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c1ccc2c(N3CCN(CCCOc4ccc5c(c4)CNC5)CC3)cccc2c1

Basic Information

ChEMBL ID CHEMBL1258312
Phase Preclinical
Structure Type MOL
InChI Key FSOQNRYVHQRTNP-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

387.5
MW (Da)
4.03
ALogP
4
HBA
1
HBD
27.7
PSA (Ų)
0.65
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 C25H29N3O
MW 387.53
Aromatic Rings 3
Heavy Atoms 29
NP-Likeness -1.01

Activity Summary

Ki 4 meas. best 9.83

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 9.83 9.83 0.1 1
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.75 8.75 1.8 1
D(2) dopamine receptor
CHEMBL217
Ki 7.47 7.47 34.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 6.11 6.11 779.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20801650 10.1016/j.bmcl.2010.08.023 5-hydroxytryptamine receptor 1A 4
20801650 10.1016/j.bmcl.2010.08.023 D(2) dopamine receptor 3
20801650 10.1016/j.bmcl.2010.08.023 5-hydroxytryptamine receptor 2A 1
20801650 10.1016/j.bmcl.2010.08.023 Voltage-gated inwardly rectifying potassium channel KCNH2 1
20801650 10.1016/j.bmcl.2010.08.023 Unchecked 1

Data from ChEMBL 36 via Core Engine