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Compound Detail

CHEMBL4206412

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CC1(C)CCN(S(=O)(=O)c2ccc(F)cc2)c2ccc(C(O)(C(F)(F)F)C(F)(F)F)cc21

Basic Information

ChEMBL ID CHEMBL4206412
Phase Preclinical
Structure Type MOL
InChI Key IFPBFPWEKKDYCO-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

485.4
MW (Da)
5.01
ALogP
3
HBA
1
HBD
57.6
PSA (Ų)
0.62
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H18F7NO3S
MW 485.42
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -0.85

Activity Summary

EC50 4 meas. best 7.44

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Nuclear receptor subfamily 1 group I member 2
CHEMBL3401
EC50 7.44 7.44 36.0 1
Oxysterols receptor LXR-alpha
CHEMBL2808
EC50 6.54 6.54 290.0 1
Oxysterols receptor LXR-beta
CHEMBL4093
EC50 6.26 6.26 550.0 1
Nuclear receptor ROR-gamma
CHEMBL1741186
EC50 6.09 6.09 815.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
29233651 10.1016/j.bmcl.2017.12.006 Nuclear receptor subfamily 1 group I member 2 2
29233651 10.1016/j.bmcl.2017.12.006 Oxysterols receptor LXR-alpha 2
29233651 10.1016/j.bmcl.2017.12.006 Oxysterols receptor LXR-beta 2
29233651 10.1016/j.bmcl.2017.12.006 Nuclear receptor ROR-gamma 1

Data from ChEMBL 36 via Core Engine