General Information of the Compound
Compound ID
CP0189282
Compound Name
N-[3-[[6-bromo-2-(4-methoxyphenyl)-1H-imidazo[4,5-b]pyridin-7-yl]amino]propyl]pyridine-3-carboxamide
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Structure
Formula
C22H21BrN6O2
Molecular Weight
481.354
Canonical SMILES
COc1ccc(cc1)-c1nc2ncc(Br)c(NCCCNC(=O)c3cccnc3)c2[nH]1
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InChI
InChI=1S/C22H21BrN6O2/c1-31-16-7-5-14(6-8-16)20-28-19-18(17(23)13-27-21(19)29-20)25-10-3-11-26-22(30)15-4-2-9-24-12-15/h2,4-9,12-13H,3,10-11H2,1H3,(H,26,30)(H2,25,27,28,29)
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InChIKey
ZEEVDVUFURMNEH-UHFFFAOYSA-N
Physicochemical Property
logP
4.023
Rotatable Bonds
8
Heavy Atom Count
31
Polar Areas
104.82
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
6
Complexity
31

"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: 70681031
ChEMBL ID
CHEMBL2011938
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: PT01682, Serine/threonine-protein kinase TBK1
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
EC50 = 87 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 59 nM