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Compound Detail

CHEMBL544091

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Cl.O=C(c1ccc(F)cc1)C1CCN(CCC2CCc3sccc3C2=O)CC1

Basic Information

ChEMBL ID CHEMBL544091
Phase Preclinical
Structure Type MOL
InChI Key UBYHUMVNSXKCLA-UHFFFAOYSA-N
Parent Compound CHEMBL109673
Active Moiety CHEMBL109673
5
Targets
5
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

385.5
MW (Da)
4.62
ALogP
4
HBA
0
HBD
37.4
PSA (Ų)
0.71
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H25ClFNO2S
MW 421.97
Aromatic Rings 2
Heavy Atoms 27
NP-Likeness -1.21

Activity Summary

Ki 4 meas. best 8.84
Kd 1 meas. best 9.02

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Kd 9.02 9.02 1.0 1
5-hydroxytryptamine receptor 2A
CHEMBL322
Ki 8.84 8.84 1.4 1
D(2) dopamine receptor
CHEMBL339
Ki 6.68 6.68 208.9 1
5-hydroxytryptamine receptor 2C
CHEMBL225
Ki 6.48 6.48 331.1 1
D(1A) dopamine receptor
CHEMBL265
Ki 5.86 5.86 1380.4 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
10425088 10.1021/jm981094e 5-hydroxytryptamine receptor 2A 3
10425088 10.1021/jm981094e Mus musculus 2
10425088 10.1021/jm981094e D(1A) dopamine receptor 1
10425088 10.1021/jm981094e D(2) dopamine receptor 1
10425088 10.1021/jm981094e 5-hydroxytryptamine receptor 2C 1
10425088 10.1021/jm981094e Unchecked 1

Data from ChEMBL 36 via Core Engine