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Compound Detail

CHEMBL453894

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

Basic Information

ChEMBL ID CHEMBL453894
Phase Preclinical
Structure Type MOL
InChI Key RDPSEAZFXPEZMP-UHFFFAOYSA-N
2
Targets
4
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

457.5
MW (Da)
5.02
ALogP
5
HBA
0
HBD
47.4
PSA (Ų)
0.55
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H26F3N3O2
MW 457.50
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness -0.79

Activity Summary

IC50 3 meas. best 9.15
Ki 1 meas. best 9.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 9.66 9.66 0.2 1
Histamine H3 receptor
CHEMBL264
IC50 9.15 9.15 0.7 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.46 6.46 350.0 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