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Compound Detail

CHEMBL4793608

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O=S(=O)(N[C@@H]1CCN(CCCc2noc3ccccc23)C1)c1csc2ccccc12

Basic Information

ChEMBL ID CHEMBL4793608
Phase Preclinical
Structure Type MOL
InChI Key VJVSHSVLEVBQER-MRXNPFEDSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

441.6
MW (Da)
4.03
ALogP
6
HBA
1
HBD
75.4
PSA (Ų)
0.47
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 C22H23N3O3S2
MW 441.58
Aromatic Rings 4
Heavy Atoms 30
NP-Likeness -1.90

Activity Summary

Ki 4 meas. best 9.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 9.38 9.38 0.4 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.93 8.93 1.2 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 8.3 8.3 5.0 1
D(2) dopamine receptor
CHEMBL217
Ki 7.7 7.7 19.9 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 3
32105980 10.1016/j.ejmech.2020.112149 5-hydroxytryptamine receptor 7 2
32105980 10.1016/j.ejmech.2020.112149 D(2) dopamine receptor 2
32105980 10.1016/j.ejmech.2020.112149 5-hydroxytryptamine receptor 6 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