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Compound Detail

CHEMBL1824230

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CN(C)[C@H]1CC[C@@H](c2ccc(OCCCN3CCCCC3)cc2)CC1

Basic Information

ChEMBL ID CHEMBL1824230
Phase Preclinical
Structure Type MOL
InChI Key NBCFVKKQKAXINS-TYKWCNGQSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

344.5
MW (Da)
4.53
ALogP
3
HBA
0
HBD
15.7
PSA (Ų)
0.68
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H36N2O
MW 344.54
Aromatic Rings 1
Heavy Atoms 25
NP-Likeness -1.07

Activity Summary

IC50 2 meas. best 4.95
Ki 2 meas. best 9.55

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL3263
Ki 9.55 9.55 0.3 1
Histamine H3 receptor
CHEMBL264
Ki 9.52 9.52 0.3 1
Cytochrome P450 2C9
CHEMBL3397
IC50 4.95 4.95 11300.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 4.3 4.3 50000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
21783360 10.1016/j.bmcl.2011.06.102 Voltage-gated inwardly rectifying potassium channel KCNH2 2
21783360 10.1016/j.bmcl.2011.06.102 Histamine H3 receptor 2
21783360 10.1016/j.bmcl.2011.06.102 Cytochrome P450 2C9 1
21783360 10.1016/j.bmcl.2011.06.102 Cytochrome P450 2D6 1
21783360 10.1016/j.bmcl.2011.06.102 Cytochrome P450 3A4 1
21783360 10.1016/j.bmcl.2011.06.102 Mus musculus 1

Data from ChEMBL 36 via Core Engine