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

CHEMBL3353238

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
O=C(Nc1ccc(C(F)(F)F)cc1)N[C@H]1CC[C@H](OCc2c(F)cccc2F)CC1

Basic Information

ChEMBL ID CHEMBL3353238
Phase Preclinical
Structure Type MOL
InChI Key DNZXTPHFQQRFFV-WKILWMFISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

428.4
MW (Da)
5.63
ALogP
2
HBA
2
HBD
50.4
PSA (Ų)
0.61
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H21F5N2O2
MW 428.40
Aromatic Rings 2
Heavy Atoms 30
NP-Likeness -1.44

Activity Summary

IC50 1 meas. best 8.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 8.36 8.36 4.4 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 4.4 nM 8.36 Inhibition of recombinant purified chicken soluble epoxide hydrolase using fluor... 25479771

Literature References

PubMed DOI Target Context # Activities
25479771 10.1016/j.bmcl.2014.11.053 Unchecked 1

Data from ChEMBL 36 via Core Engine