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Compound Detail

CHEMBL5092755

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Cc1ccc(S(=O)(=O)CC2CCN(CCCc3noc4cc(F)ccc34)C2)cc1C

Basic Information

ChEMBL ID CHEMBL5092755
Phase Preclinical
Structure Type MOL
InChI Key NQGAZHMNNANZRL-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

430.6
MW (Da)
4.31
ALogP
5
HBA
0
HBD
63.4
PSA (Ų)
0.56
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 C23H27FN2O3S
MW 430.55
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -1.76

Activity Summary

Ki 4 meas. best 8.77

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.77 8.77 1.7 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.08 8.08 8.3 1
D(2) dopamine receptor
CHEMBL217
Ki 7.7 7.7 19.9 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 6.69 6.69 204.2 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