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Compound Detail

CHEMBL2037529

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O=C(CCCCN1CCN(c2ncccn2)CC1)c1nc2ccccc2s1

Basic Information

ChEMBL ID CHEMBL2037529
Phase Preclinical
Structure Type MOL
InChI Key DYFDYWXRTZSUEM-UHFFFAOYSA-N
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
7
Publications
0
Known Names

Molecular Properties

381.5
MW (Da)
3.26
ALogP
7
HBA
0
HBD
62.2
PSA (Ų)
0.46
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 C20H23N5OS
MW 381.51
Aromatic Rings 3
Heavy Atoms 27
NP-Likeness -1.84

Activity Summary

Ki 5 meas. best 8.44

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 8.44 8.44 3.6 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 6.47 6.47 337.0 1
D(4) dopamine receptor
CHEMBL3361
Ki 6.46 6.46 346.0 1
D(2) dopamine receptor
CHEMBL217
Ki 6.3 6.3 505.0 1
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 5.16 5.16 6982.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22520153 10.1016/j.ejmech.2012.03.042 5-hydroxytryptamine receptor 1A 1
22520153 10.1016/j.ejmech.2012.03.042 Sodium-dependent serotonin transporter 1
22520153 10.1016/j.ejmech.2012.03.042 5-hydroxytryptamine receptor 2A 1
22520153 10.1016/j.ejmech.2012.03.042 5-hydroxytryptamine receptor 2C 1
22520153 10.1016/j.ejmech.2012.03.042 5-hydroxytryptamine receptor 7 1
22520153 10.1016/j.ejmech.2012.03.042 D(2) dopamine receptor 1
22520153 10.1016/j.ejmech.2012.03.042 D(4) dopamine receptor 1

Data from ChEMBL 36 via Core Engine