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Compound Detail

CHEMBL5088232

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C[C@H]1C[C@H](NS(=O)(=O)c2ccc3ccccc3c2)CN1CCCc1noc2cc(F)ccc12

Basic Information

ChEMBL ID CHEMBL5088232
Phase Preclinical
Structure Type MOL
InChI Key HLGKXVMBSLHNKH-UWJYYQICSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

467.6
MW (Da)
4.49
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 C25H26FN3O3S
MW 467.57
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.46

Activity Summary

Ki 4 meas. best 8.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.82 8.82 1.5 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.11 8.11 7.8 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 7.36 7.36 43.6 1
D(2) dopamine receptor
CHEMBL217
Ki 7.33 7.33 46.8 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