General Information of the Compound
Compound ID
CP0387061
Compound Name
1-[3-(2,2-dimethylpropanoylamino)propyl]-2-[(2-ethyl-5-methylpyrazole-3-carbonyl)amino]-7-methoxybenzimidazole-5-carboxamide
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Structure
Formula
C24H33N7O4
Molecular Weight
483.573
Canonical SMILES
CCn1nc(C)cc1C(=O)Nc1nc2cc(cc(OC)c2n1CCCNC(=O)C(C)(C)C)C(N)=O
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InChI
InChI=1S/C24H33N7O4/c1-7-31-17(11-14(2)29-31)21(33)28-23-27-16-12-15(20(25)32)13-18(35-6)19(16)30(23)10-8-9-26-22(34)24(3,4)5/h11-13H,7-10H2,1-6H3,(H2,25,32)(H,26,34)(H,27,28,33)
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InChIKey
DDCZFXJEDYZLDW-UHFFFAOYSA-N
Physicochemical Property
logP
2.47332
Rotatable Bonds
9
Heavy Atom Count
35
Polar Areas
146.16
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
8
Complexity
35

"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: 155568518
ChEMBL ID
CHEMBL4591496
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 = 27500 nM
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   LI
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   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