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Compound Detail

CHEMBL257704

EPLIVANSERIN
🧪 Phase III
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🧪 Phase III
CN(C)CCO/N=C(/C=C/c1ccc(O)cc1)c1ccccc1F

Basic Information

ChEMBL ID CHEMBL257704
Name EPLIVANSERIN
Phase Phase III
Structure Type MOL
InChI Key VAIOZOCLKVMIMN-PRJWTAEASA-N

Known Names

Eplivanserin Eplivanserina Eplivanserine SR-46349 SR46349
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
7
Publications
5
Known Names
2
Indications
1
Mechanisms

Molecular Properties

328.4
MW (Da)
3.53
ALogP
4
HBA
1
HBD
45.1
PSA (Ų)
0.48
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Chirality Achiral
USAN Stem -anserin
USAN Year 2009

Extended Properties

Molecular Formula C19H21FN2O2
MW 328.39
Aromatic Rings 2
Heavy Atoms 24
NP-Likeness -0.57

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Serotonin 2a (5-HT2a) receptor antagonist ANTAGONIST 5-hydroxytryptamine receptor 2A

Indications

Sleep Initiation and Maintenance Disorders Sleep Wake Disorders

Activity Summary

Kd 1 meas. best 8.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Serotonin 2 (5-HT2) receptor
CHEMBL2095200
Kd 8.92 8.92 1.2 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL4495565 SARS-CoV-2 2
- 10.6019/CHEMBL4651402 SARS-CoV-2 2
18282705 10.1016/j.bmcl.2008.01.090 5-hydroxytryptamine receptor 2B 1
18282705 10.1016/j.bmcl.2008.01.090 5-hydroxytryptamine receptor 2C 1
18282705 10.1016/j.bmcl.2008.01.090 5-hydroxytryptamine receptor 2A 1
- 10.6019/CHEMBL4495564 Replicase polyprotein 1ab 1
35939391 10.1021/acs.jmedchem.2c00633 Serotonin 2 (5-HT2) receptor 1

Data from ChEMBL 36 via Core Engine