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Compound Detail

CHEMBL218834

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CC(C)N1CCN(C(=O)N2CCC(C(=O)N3CC4CCC(CC4)C3)CC2)CC1

Basic Information

ChEMBL ID CHEMBL218834
Phase Preclinical
Structure Type MOL
InChI Key UQKFKOGOHFMDDR-UHFFFAOYSA-N
1
Targets
3
Activities
2
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

390.6
MW (Da)
2.49
ALogP
3
HBA
0
HBD
47.1
PSA (Ų)
0.73
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H38N4O2
MW 390.57
Aromatic Rings 0
Heavy Atoms 28
NP-Likeness -1.16

Activity Summary

Ki 2 meas. best 7.85
IC50 1 meas.

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 7.85 7.85 14.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
16908150 10.1016/j.bmcl.2006.07.093 Histamine H3 receptor 1
16908150 10.1016/j.bmcl.2006.07.093 Voltage-gated inwardly rectifying potassium channel KCNH2 1
16908150 10.1016/j.bmcl.2006.07.093 Cytochrome P450 1A2 1
16908150 10.1016/j.bmcl.2006.07.093 Cytochrome P450 3A4 1
16908150 10.1016/j.bmcl.2006.07.093 Cytochrome P450 2D6 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