Structure

InChI Key LTSUMTMGJHPGFX-UHFFFAOYSA-N
Smiles O=C(O)Cc1ccc(Cc2cc(-c3cccc(Cl)c3)nc(C(F)(F)F)c2)cc1
InChI
InChI=1S/C21H15ClF3NO2/c22-17-3-1-2-16(12-17)18-9-15(10-19(26-18)21(23,24)25)8-13-4-6-14(7-5-13)11-20(27)28/h1-7,9-10,12H,8,11H2,(H,27,28)

Physicochemical Descriptors

Property Name Value
Molecular Formula C21H15ClF3NO2
Molecular Weight 405.8
AlogP 5.64
Hydrogen Bond Acceptor 2.0
Hydrogen Bond Donor 1.0
Number of Rotational Bond 5.0
Polar Surface Area 50.19
Molecular species ACID
Aromatic Rings 3.0
Heavy Atoms 28.0

Pharmacology

Mechanism of Action Action Reference
Phosphodiesterase 4D inhibitor INHIBITOR PubMed Other
Targets EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Enzyme Phosphodiesterase Phosphodiesterase 4 Phosphodiesterase 4D
- 127 - - -
EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Homo sapiens
- 2.9-133 - - -

Target Conservation

Protein: Phosphodiesterase 4D

Description: cAMP-specific 3',5'-cyclic phosphodiesterase 4D

Organism : Homo sapiens

Q08499 ENSG00000113448

Cross References

Resources Reference
ChEMBL CHEMBL4541964
FDA SRS G786V328X6
Guide to Pharmacology 10451
PDB KR7
SureChEMBL SCHEMBL15660260