General Information of the Compound
Compound ID
CP0128025
Compound Name
4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-6-((dimethylamino)methyl)-1-ethyl-1H-imidazo[4,5-c]pyridin-4-yl)-2-methylbut-3-yn-2-ol
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Structure
Formula
C18H23N7O2
Molecular Weight
369.429
Canonical SMILES
CCn1c(nc2c(nc(CN(C)C)cc12)C#CC(C)(C)O)-c1nonc1N
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InChI
InChI=1S/C18H23N7O2/c1-6-25-13-9-11(10-24(4)5)20-12(7-8-18(2,3)26)14(13)21-17(25)15-16(19)23-27-22-15/h9,26H,6,10H2,1-5H3,(H2,19,23)
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InChIKey
GFWBYAUCYFKBRF-UHFFFAOYSA-N
Physicochemical Property
logP
1.2674
Rotatable Bonds
4
Heavy Atom Count
27
Polar Areas
119.12
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
9
Complexity
27

"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: 11959378
SID: 17417676
ChEMBL ID
CHEMBL1099290
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: PT00962, Glycogen synthase kinase-3 beta
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000218 BT-474 Homo sapiens (Human)  1
1
IC50 = 375 nM
   TI
   LI
   LO
   TS
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000141 LNCaP Homo sapiens (Human)  1
1
IC50 = 114 nM
   TI
   LI
   LO
   TS
CL000218 BT-474 Homo sapiens (Human)  1
1
IC50 = 357 nM
   TI
   LI
   LO
   TS