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Compound Detail

CHEMBL252228

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CCCC(=O)NC1CCc2cc(CCN3CCN(c4nsc5ccccc45)CC3)ccc21

Basic Information

ChEMBL ID CHEMBL252228
Phase Preclinical
Structure Type MOL
InChI Key KVDPUCCGORKFOD-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

448.6
MW (Da)
4.56
ALogP
5
HBA
1
HBD
48.5
PSA (Ų)
0.58
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 C26H32N4OS
MW 448.64
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -1.27

Activity Summary

Ki 4 meas. best 9.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 9.3 9.3 0.5 1
Alpha-1A adrenergic receptor
CHEMBL319
Ki 9.05 9.05 0.9 1
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 8.7 8.7 2.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 6.57 6.57 269.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18160289 10.1016/j.bmcl.2007.11.106 5-hydroxytryptamine receptor 1A 2
18160289 10.1016/j.bmcl.2007.11.106 D(2) dopamine receptor 1
18160289 10.1016/j.bmcl.2007.11.106 5-hydroxytryptamine receptor 2A 1
18160289 10.1016/j.bmcl.2007.11.106 Alpha-1A adrenergic receptor 1
18160289 10.1016/j.bmcl.2007.11.106 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine