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Compound Detail

CHEMBL454642

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Cn1c(-c2ccc(OC3CCN(C4CCC4)CC3)cc2)nc2c(F)cccc2c1=O

Basic Information

ChEMBL ID CHEMBL454642
Phase Preclinical
Structure Type MOL
InChI Key QMDIXUJXXUMWBD-UHFFFAOYSA-N
3
Targets
5
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

407.5
MW (Da)
4.14
ALogP
5
HBA
0
HBD
47.4
PSA (Ų)
0.65
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 C24H26FN3O2
MW 407.49
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -0.91

Activity Summary

IC50 4 meas. best 9.6
Ki 1 meas. best 10.11

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 10.11 10.11 0.1 1
Histamine H3 receptor
CHEMBL264
IC50 9.6 9.6 0.2 1
Alpha-1A adrenergic receptor
CHEMBL229
IC50 5.35 5.35 4500.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.1 5.1 7900.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18952421 10.1016/j.bmcl.2008.10.034 Histamine H3 receptor 1
18952421 10.1016/j.bmcl.2008.10.034 Voltage-gated inwardly rectifying potassium channel KCNH2 1
18952421 10.1016/j.bmcl.2008.10.034 Alpha-1A adrenergic receptor 1
21802950 10.1016/j.bmcl.2011.07.006 Histamine H3 receptor 1
21802950 10.1016/j.bmcl.2011.07.006 Voltage-gated inwardly rectifying potassium channel KCNH2 1
21802950 10.1016/j.bmcl.2011.07.006 No relevant target 1

Data from ChEMBL 36 via Core Engine