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Compound Detail

CHEMBL4748107

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O=S(=O)(N[C@H]1CCN(CCCc2noc3ccccc23)C1)c1ccc2cc(Cl)ccc2c1

Basic Information

ChEMBL ID CHEMBL4748107
Phase Preclinical
Structure Type MOL
InChI Key QUGHLFHSMAECME-FQEVSTJZSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

470.0
MW (Da)
4.62
ALogP
5
HBA
1
HBD
75.4
PSA (Ų)
0.43
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H24ClN3O3S
MW 469.99
Aromatic Rings 4
Heavy Atoms 32
NP-Likeness -1.89

Activity Summary

Ki 4 meas. best 7.71

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 7.71 7.71 19.5 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.61 7.61 24.6 1
D(2) dopamine receptor
CHEMBL217
Ki 6.99 6.99 102.3 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 6.61 6.61 245.5 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
32105980 10.1016/j.ejmech.2020.112149 5-hydroxytryptamine receptor 2A 1
32105980 10.1016/j.ejmech.2020.112149 5-hydroxytryptamine receptor 6 1
32105980 10.1016/j.ejmech.2020.112149 5-hydroxytryptamine receptor 7 1
32105980 10.1016/j.ejmech.2020.112149 D(2) dopamine receptor 1
32105980 10.1016/j.ejmech.2020.112149 Muscarinic acetylcholine receptor M3 1
32105980 10.1016/j.ejmech.2020.112149 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine