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Compound Detail

CHEMBL1097160

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CS(=O)(=O)c1cc(-c2cccc(-c3ccnc4c(C(F)(F)F)cccc34)c2)ccc1F

Basic Information

ChEMBL ID CHEMBL1097160
Phase Preclinical
Structure Type MOL
InChI Key QIFYDQQBXMOQLW-UHFFFAOYSA-N
4
Targets
5
Activities
2
Assay Types
2
PK Parameters
6
Publications
0
Known Names

Molecular Properties

445.4
MW (Da)
6.13
ALogP
3
HBA
0
HBD
47.0
PSA (Ų)
0.36
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 C23H15F4NO2S
MW 445.44
Aromatic Rings 4
Heavy Atoms 31
NP-Likeness -1.15

Activity Summary

EC50 3 meas. best 7.39
IC50 2 meas. best 8.59

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Oxysterols receptor LXR-beta
CHEMBL4093
IC50 8.59 8.59 2.6 1
Oxysterols receptor LXR-alpha
CHEMBL2808
IC50 7.5 7.5 32.0 1
HepG2
CHEMBL395
EC50 7.39 7.39 41.0 1
J774
CHEMBL614123
EC50 6.85 6.85 140.0 1
Oxysterols receptor LXR-beta
CHEMBL4093
EC50 6.29 6.29 512.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.2 hr Rattus norvegicus
T1/2 0.5 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20382019 10.1016/j.bmcl.2010.03.031 Oxysterols receptor LXR-beta 3
20382019 10.1016/j.bmcl.2010.03.031 Liver microsomes 2
20382019 10.1016/j.bmcl.2010.03.031 J774 2
20382019 10.1016/j.bmcl.2010.03.031 HepG2 2
20382019 10.1016/j.bmcl.2010.03.031 Oxysterols receptor LXR-alpha 1
20382019 10.1016/j.bmcl.2010.03.031 Huh-7 1

Data from ChEMBL 36 via Core Engine