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Compound Detail

CHEMBL2059324

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O=C1COc2ccccc2N1CCCN1CCC(n2c(=O)[nH]c3c(F)cccc32)CC1

Basic Information

ChEMBL ID CHEMBL2059324
Phase Preclinical
Structure Type MOL
InChI Key LRXGBYNAHIRXGB-UHFFFAOYSA-N
3
Targets
3
Activities
3
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

424.5
MW (Da)
2.92
ALogP
5
HBA
1
HBD
70.6
PSA (Ų)
0.68
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 C23H25FN4O3
MW 424.48
Aromatic Rings 3
Heavy Atoms 31
NP-Likeness -1.51

Activity Summary

EC50 1 meas. best 6.96
IC50 1 meas. best 5.47
Ki 1 meas. best 7.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
D(2) dopamine receptor
CHEMBL217
Ki 7.82 7.82 15.0 1
Muscarinic acetylcholine receptor M1
CHEMBL216
EC50 6.96 6.96 110.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.47 5.47 3400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22677319 10.1016/j.bmcl.2012.05.048 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