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Compound Detail

CHEMBL2401750

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CC(=O)N1CCC(CN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1

Basic Information

ChEMBL ID CHEMBL2401750
Phase Preclinical
Structure Type MOL
InChI Key LPYIFDLQYWSXGD-UHFFFAOYSA-N
2
Targets
3
Activities
2
Assay Types
1
PK Parameters
5
Publications
0
Known Names

Molecular Properties

439.6
MW (Da)
3.39
ALogP
4
HBA
2
HBD
81.3
PSA (Ų)
0.72
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 C25H37N5O2
MW 439.60
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -1.35

Activity Summary

Ki 2 meas. best 9.0
EC50 1 meas. best 8.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 4
CHEMBL1875
Ki 9.0 9.0 1.0 1
5-hydroxytryptamine receptor 4
CHEMBL1875
EC50 8.8 8.8 1.6 1
5-hydroxytryptamine receptor 3A
CHEMBL1899
Ki 4.0 4.0 100000.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.5 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
23756062 10.1016/j.bmcl.2013.05.018 5-hydroxytryptamine receptor 4 3
23756062 10.1016/j.bmcl.2013.05.018 Liver microsomes 1
23756062 10.1016/j.bmcl.2013.05.018 Voltage-gated inwardly rectifying potassium channel KCNH2 1
23756062 10.1016/j.bmcl.2013.05.018 Caco-2 1
23756062 10.1016/j.bmcl.2013.05.018 5-hydroxytryptamine receptor 3A 1

Data from ChEMBL 36 via Core Engine