General Information of the Compound
Compound ID
CP0537025
Compound Name
7-methoxy-2-[(3-methylimidazole-4-carbonyl)amino]-1-propylbenzimidazole-5-carboxamide
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Structure
Formula
C17H20N6O3
Molecular Weight
356.386
Canonical SMILES
CCCn1c(NC(=O)c2cncn2C)nc2cc(cc(OC)c12)C(N)=O
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InChI
InChI=1S/C17H20N6O3/c1-4-5-23-14-11(6-10(15(18)24)7-13(14)26-3)20-17(23)21-16(25)12-8-19-9-22(12)2/h6-9H,4-5H2,1-3H3,(H2,18,24)(H,20,21,25)
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InChIKey
YDDVDVNMRRLXSL-UHFFFAOYSA-N
Physicochemical Property
logP
1.5396
Rotatable Bonds
6
Heavy Atom Count
26
Polar Areas
117.06
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
7
Complexity
26

"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: 155562008
ChEMBL ID
CHEMBL4584615
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