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Compound Detail

CHEMBL5087742

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C[C@H]1C[C@H](NS(=O)(=O)c2csc3ccccc23)CN1CCCc1noc2cc(F)ccc12

Basic Information

ChEMBL ID CHEMBL5087742
Phase Preclinical
Structure Type MOL
InChI Key HDJYJCCQWSDIIV-RDJZCZTQSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

473.6
MW (Da)
4.56
ALogP
6
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 C23H24FN3O3S2
MW 473.60
Aromatic Rings 4
Heavy Atoms 32
NP-Likeness -1.64

Activity Summary

Ki 4 meas. best 8.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.38 8.38 4.2 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.58 7.58 26.3 1
D(2) dopamine receptor
CHEMBL217
Ki 7.27 7.27 53.7 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 7.02 7.02 95.5 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34436892 10.1021/acs.jmedchem.1c00497 5-hydroxytryptamine receptor 2A 2
34436892 10.1021/acs.jmedchem.1c00497 5-hydroxytryptamine receptor 6 2
34436892 10.1021/acs.jmedchem.1c00497 5-hydroxytryptamine receptor 7 2
34436892 10.1021/acs.jmedchem.1c00497 D(2) dopamine receptor 2
34436892 10.1021/acs.jmedchem.1c00497 Muscarinic acetylcholine receptor M1 1
34436892 10.1021/acs.jmedchem.1c00497 Histamine H1 receptor 1
34436892 10.1021/acs.jmedchem.1c00497 Alpha-1A adrenergic receptor 1
34436892 10.1021/acs.jmedchem.1c00497 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine