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Compound Detail

CHEMBL453653

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COc1cccc2nc(-c3ccc(OC4CCN(C5CCC5)CC4)cc3)n(C)c(=O)c12

Basic Information

ChEMBL ID CHEMBL453653
Phase Preclinical
Structure Type MOL
InChI Key HVRHVFJBNXLKGN-UHFFFAOYSA-N
3
Targets
4
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

419.5
MW (Da)
4.00
ALogP
6
HBA
0
HBD
56.6
PSA (Ų)
0.63
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 C25H29N3O3
MW 419.53
Aromatic Rings 3
Heavy Atoms 31
NP-Likeness -0.52

Activity Summary

IC50 3 meas. best 9.27
Ki 1 meas. best 9.81

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 9.81 9.81 0.2 1
Histamine H3 receptor
CHEMBL264
IC50 9.27 9.27 0.5 1
Alpha-1A adrenergic receptor
CHEMBL229
IC50 5.38 5.38 4200.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.0 5.0 10000.0 1

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