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Compound Detail

CHEMBL1935590

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O=S(=O)(c1cccc(F)c1)c1ccc2c3c(oc2c1)CNCC3

Basic Information

ChEMBL ID CHEMBL1935590
Phase Preclinical
Structure Type MOL
InChI Key WDRSQVMCYDMWAP-UHFFFAOYSA-N
3
Targets
4
Activities
2
Assay Types
2
PK Parameters
4
Publications
0
Known Names

Molecular Properties

331.4
MW (Da)
3.05
ALogP
4
HBA
1
HBD
59.3
PSA (Ų)
0.78
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H14FNO3S
MW 331.37
Aromatic Rings 3
Heavy Atoms 23
NP-Likeness -1.01

Activity Summary

IC50 2 meas. best 8.44
Ki 2 meas. best 8.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.8 8.8 1.6 1
5-hydroxytryptamine receptor 6
CHEMBL3371
IC50 8.44 8.44 3.6 1
5-hydroxytryptamine receptor 6
CHEMBL3372
Ki 8.16 8.16 6.9 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.0 6.0 1000.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.1717 hr Canis lupus familiaris
T1/2 0.08333 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22153937 10.1016/j.bmcl.2011.11.050 5-hydroxytryptamine receptor 6 3
22153937 10.1016/j.bmcl.2011.11.050 Liver 1
22153937 10.1016/j.bmcl.2011.11.050 Liver microsomes 1
22153937 10.1016/j.bmcl.2011.11.050 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine