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Compound Detail

CHEMBL442290

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O=C(NC1CCc2ccc(CCN3CCN(c4nsc5ccccc45)CC3)cc21)c1ccc(F)cc1

Basic Information

ChEMBL ID CHEMBL442290
Phase Preclinical
Structure Type MOL
InChI Key ZBUMCITULAAXBQ-UHFFFAOYSA-N
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

500.6
MW (Da)
5.22
ALogP
5
HBA
1
HBD
48.5
PSA (Ų)
0.39
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H29FN4OS
MW 500.64
Aromatic Rings 4
Heavy Atoms 36
NP-Likeness -1.39

Activity Summary

Ki 5 meas. best 8.61

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.61 8.61 2.5 1
D(2) dopamine receptor
CHEMBL217
Ki 8.22 8.22 6.0 1
Alpha-1A adrenergic receptor
CHEMBL319
Ki 7.99 7.99 10.3 1
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 7.18 7.18 66.7 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 7.11 7.11 78.0 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