General Information of the Compound
Compound ID
CP0457255
Compound Name
1-(2-Imidazol-1-yl-1-phenyl-ethyl)-3-(4-trifluoromethyl-phenyl)-1H-pyridin-2-one
    Show/Hide
Structure
Formula
C23H18F3N3O
Molecular Weight
409.411
Canonical SMILES
FC(F)(F)c1ccc(cc1)-c1cccn(C(Cn2ccnc2)c2ccccc2)c1=O
    Show/Hide
InChI
InChI=1S/C23H18F3N3O/c24-23(25,26)19-10-8-17(9-11-19)20-7-4-13-29(22(20)30)21(15-28-14-12-27-16-28)18-5-2-1-3-6-18/h1-14,16,21H,15H2
    Show/Hide
InChIKey
KCGULYCKVHGSFH-UHFFFAOYSA-N
Physicochemical Property
logP
5.0202
Rotatable Bonds
5
Heavy Atom Count
30
Polar Areas
39.82
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Complexity
30

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

    Show/Hide
Click to Show/Hide the External Link(s) of This Compound
PubChem ID
CID: 44269900
ChEMBL ID
CHEMBL418351
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT00983, Kappa-type opioid receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 > 10000 nM
   TI
   LI
   LO
   TS