General Information of the Compound
Compound ID
CP0356387
Compound Name
4-[(2S)-2-(1,6-dimethylbenzimidazol-2-yl)-2-[2,5-dioxo-3-(4-phenoxyphenyl)imidazolidin-1-yl]ethyl]benzonitrile
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Structure
Formula
C33H27N5O3
Molecular Weight
541.611
Canonical SMILES
Cc1ccc2nc([C@H](Cc3ccc(cc3)C#N)N3C(=O)CN(C3=O)c3ccc(Oc4ccccc4)cc3)n(C)c2c1
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InChI
InChI=1S/C33H27N5O3/c1-22-8-17-28-29(18-22)36(2)32(35-28)30(19-23-9-11-24(20-34)12-10-23)38-31(39)21-37(33(38)40)25-13-15-27(16-14-25)41-26-6-4-3-5-7-26/h3-18,30H,19,21H2,1-2H3/t30-/m0/s1
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InChIKey
CXQRHIDVBFSQPN-PMERELPUSA-N
Physicochemical Property
logP
6.2983
Rotatable Bonds
7
Heavy Atom Count
41
Polar Areas
91.46
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
6
Complexity
41

"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).

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PubChem ID
CID: 155523003
ChEMBL ID
CHEMBL4453727
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: PT01286, Bile acid receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000148 Huh-7 Homo sapiens (Human)  1
1
IC50 = 781 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 7100 nM
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000148 Huh-7 Homo sapiens (Human)  1
1
IC50 > 100000 nM
   TI
   LI
   LO
   TS