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Compound Detail

CHEMBL5084167

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O=S(=O)(CC1CCN(CCCc2noc3cc(F)ccc23)C1)c1ccc2ccccc2c1

Basic Information

ChEMBL ID CHEMBL5084167
Phase Preclinical
Structure Type MOL
InChI Key WIJVLCXKSPDTFW-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
1
PK Parameters
9
Publications
0
Known Names

Molecular Properties

452.6
MW (Da)
4.85
ALogP
5
HBA
0
HBD
63.4
PSA (Ų)
0.40
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 C25H25FN2O3S
MW 452.55
Aromatic Rings 4
Heavy Atoms 32
NP-Likeness -1.53

Activity Summary

Ki 4 meas. best 9.61

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 9.61 9.61 0.2 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.33 8.33 4.7 1
D(2) dopamine receptor
CHEMBL217
Ki 8.28 8.28 5.2 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 7.81 7.81 15.5 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.3833 hr Homo sapiens

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
34436892 10.1021/acs.jmedchem.1c00497 ADMET 1

Data from ChEMBL 36 via Core Engine