Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL206307

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
N#Cc1ccccc1S(=O)(=O)N1CCC(CCc2ccc(F)cc2F)CC1

Basic Information

ChEMBL ID CHEMBL206307
Phase Preclinical
Structure Type MOL
InChI Key YMCDAGKBVRZKSE-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

390.5
MW (Da)
3.87
ALogP
3
HBA
0
HBD
61.2
PSA (Ų)
0.78
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H20F2N2O2S
MW 390.46
Aromatic Rings 2
Heavy Atoms 27
NP-Likeness -1.94

Activity Summary

Ki 2 meas. best 8.09

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.09 8.09 8.1 1
5-hydroxytryptamine receptor 2C
CHEMBL225
Ki 7.16 7.16 70.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
16632354 10.1016/j.bmcl.2006.03.050 5-hydroxytryptamine receptor 2A 1
16632354 10.1016/j.bmcl.2006.03.050 5-hydroxytryptamine receptor 2C 1
16632354 10.1016/j.bmcl.2006.03.050 Serotonin 2 receptors; 5-HT2a & 5-HT2c 1
16632354 10.1016/j.bmcl.2006.03.050 D(2) dopamine receptor 1
16632354 10.1016/j.bmcl.2006.03.050 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine