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Compound Detail

CHEMBL252429

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O=C(NC1CCc2cc(CCN3CCN(c4nsc5ccccc45)CC3)ccc21)c1ccc(F)cc1

Basic Information

ChEMBL ID CHEMBL252429
Phase Preclinical
Structure Type MOL
InChI Key PHCUGENQVJPTLC-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 -1.42

Activity Summary

Ki 5 meas. best 8.78

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.78 8.78 1.6 1
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 8.11 8.11 7.8 1
D(2) dopamine receptor
CHEMBL217
Ki 8.0 8.0 10.0 1
Alpha-1A adrenergic receptor
CHEMBL319
Ki 7.81 7.81 15.6 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 6.87 6.87 135.0 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