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Compound Detail

CHEMBL252230

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O=C(NC1CCc2cc(CCN3CCN(c4nsc5ccccc45)CC3)ccc21)C1CC1

Basic Information

ChEMBL ID CHEMBL252230
Phase Preclinical
Structure Type MOL
InChI Key LSIUKLXQSPBSEE-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

446.6
MW (Da)
4.17
ALogP
5
HBA
1
HBD
48.5
PSA (Ų)
0.62
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 C26H30N4OS
MW 446.62
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -1.41

Activity Summary

Ki 4 meas. best 9.35

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 9.35 9.35 0.5 1
Alpha-1A adrenergic receptor
CHEMBL319
Ki 9.14 9.14 0.7 1
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 8.7 8.7 2.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 6.86 6.86 137.0 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