General Information of the Compound
Compound ID
CP0455878
Compound Name
7-methoxy-2-[(1-methylindole-2-carbonyl)amino]-1-propylbenzimidazole-5-carboxamide
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Structure
Formula
C22H23N5O3
Molecular Weight
405.458
Canonical SMILES
CCCn1c(NC(=O)c2cc3ccccc3n2C)nc2cc(cc(OC)c12)C(N)=O
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InChI
InChI=1S/C22H23N5O3/c1-4-9-27-19-15(10-14(20(23)28)12-18(19)30-3)24-22(27)25-21(29)17-11-13-7-5-6-8-16(13)26(17)2/h5-8,10-12H,4,9H2,1-3H3,(H2,23,28)(H,24,25,29)
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InChIKey
QUQNTSOVKFWUDZ-UHFFFAOYSA-N
Physicochemical Property
logP
3.2978
Rotatable Bonds
6
Heavy Atom Count
30
Polar Areas
104.17
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
6
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).

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PubChem ID
CID: 155554979
ChEMBL ID
CHEMBL4551388
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: PT03644, Stimulator of interferon genes protein
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000040 THP-1 Homo sapiens (Human)  1
1
EC50 > 100000 nM
   TI
   LI
   LO
   TS
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000040 THP-1 Homo sapiens (Human)  1
1
IC50 > 100000 nM
   TI
   LI
   LO
   TS