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Compound Detail

CHEMBL3753093

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CC(C)N1CCC(Oc2ccc(C(=O)NC3CCN(C(C)C)C3)cc2)CC1

Basic Information

ChEMBL ID CHEMBL3753093
Phase Preclinical
Structure Type MOL
InChI Key MLNZYIQIFPHNKO-UHFFFAOYSA-N
1
Targets
3
Activities
2
Assay Types
6
PK Parameters
6
Publications
0
Known Names

Molecular Properties

373.5
MW (Da)
3.15
ALogP
4
HBA
1
HBD
44.8
PSA (Ų)
0.83
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H35N3O2
MW 373.54
Aromatic Rings 1
Heavy Atoms 27
NP-Likeness -1.12

Activity Summary

Ki 2 meas. best 9.05
IC50 1 meas. best 6.49

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 9.05 8.645 0.9 2
Histamine H3 receptor
CHEMBL264
IC50 6.49 6.49 323.8 1

Pharmacokinetic Data

Parameter Value Units Species
AUC 444.0 ng.hr.mL-1 Rattus norvegicus
CL 1.5 mL.min-1.kg-1 Rattus norvegicus
Cmax 326.6 nM Rattus norvegicus
F 75.0 % Rattus norvegicus
T1/2 11.67 hr Rattus norvegicus
Vd 0.119 L.kg-1 Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
26731168 10.1016/j.ejmech.2015.12.005 Rattus norvegicus 6
26731168 10.1016/j.ejmech.2015.12.005 Histamine H3 receptor 3
26731168 10.1016/j.ejmech.2015.12.005 Liver microsome 2
26731168 10.1016/j.ejmech.2015.12.005 Voltage-gated inwardly rectifying potassium channel KCNH2 1
26731168 10.1016/j.ejmech.2015.12.005 Cytochrome P450 3A4 1
26731168 10.1016/j.ejmech.2015.12.005 Cytochrome P450 2D6 1

Data from ChEMBL 36 via Core Engine