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Compound Detail

CHEMBL176109

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O=S(=O)(c1ccc(N2CCC2)cc1)C1(F)CCN(CCc2ccc(F)cc2F)CC1

Basic Information

ChEMBL ID CHEMBL176109
Phase Preclinical
Structure Type MOL
InChI Key WCUXCSHIFAMMQM-UHFFFAOYSA-N
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

438.5
MW (Da)
3.95
ALogP
4
HBA
0
HBD
40.6
PSA (Ų)
0.68
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H25F3N2O2S
MW 438.52
Aromatic Rings 2
Heavy Atoms 30
NP-Likeness -1.54

Activity Summary

Ki 5 meas. best 9.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL322
Ki 9.52 9.52 0.3 1
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 9.0 9.0 1.0 1
5-hydroxytryptamine receptor 2C
CHEMBL225
Ki 6.07 6.07 844.0 1
D(2) dopamine receptor
CHEMBL217
Ki 5.7 5.7 2000.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 5.0 5.0 9971.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15993598 10.1016/j.bmcl.2005.05.104 5-hydroxytryptamine receptor 2A 3
15993598 10.1016/j.bmcl.2005.05.104 5-hydroxytryptamine receptor 2C 1
15993598 10.1016/j.bmcl.2005.05.104 D(2) dopamine receptor 1
15993598 10.1016/j.bmcl.2005.05.104 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine