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Compound Detail

CHEMBL1323386

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O=S1(=O)c2ccccc2N(Cc2ccc(Cl)cc2F)c2ccccc21

Basic Information

ChEMBL ID CHEMBL1323386
Phase Preclinical
Structure Type MOL
InChI Key JTSLXNXALUZZHT-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

373.8
MW (Da)
4.96
ALogP
3
HBA
0
HBD
37.4
PSA (Ų)
0.64
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 C19H13ClFNO2S
MW 373.84
Aromatic Rings 3
Heavy Atoms 25
NP-Likeness -1.62

Activity Summary

Ki 4 meas. best 5.56

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 5.56 5.56 2745.0 1
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 5.41 5.41 3866.0 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 5.28 5.28 5232.0 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 4.88 4.88 13330.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
25866241 10.1016/j.bmcl.2015.03.049 5-hydroxytryptamine receptor 6 1
25866241 10.1016/j.bmcl.2015.03.049 5-hydroxytryptamine receptor 1A 1
25866241 10.1016/j.bmcl.2015.03.049 5-hydroxytryptamine receptor 2A 1
25866241 10.1016/j.bmcl.2015.03.049 5-hydroxytryptamine receptor 7 1
25866241 10.1016/j.bmcl.2015.03.049 No relevant target 1

Data from ChEMBL 36 via Core Engine