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Compound Detail

CHEMBL508712

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Cc1cccc2c(=O)n(C)c(-c3ccc(OC4CCN(C5CCC5)CC4)cc3)nc12

Basic Information

ChEMBL ID CHEMBL508712
Phase Preclinical
Structure Type MOL
InChI Key FZAFEIPWODBIGS-UHFFFAOYSA-N
3
Targets
5
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

403.5
MW (Da)
4.30
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 C25H29N3O2
MW 403.53
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -0.76

Activity Summary

IC50 4 meas. best 10.0
Ki 1 meas. best 10.51

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 10.51 10.51 0.0 1
Histamine H3 receptor
CHEMBL264
IC50 10.0 10.0 0.1 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.7 5.7 2000.0 2
Alpha-1A adrenergic receptor
CHEMBL229
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