General Information of the Compound
Compound ID
CP0313931
Compound Name
4-[[4-(4-methoxy-6-morpholin-4-yl-1,3,5-triazin-2-yl)phenyl]carbamoylamino]-N-(2-piperidin-1-ylethyl)benzamide
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Structure
Formula
C29H36N8O4
Molecular Weight
560.659
Canonical SMILES
COc1nc(nc(n1)-c1ccc(NC(=O)Nc2ccc(cc2)C(=O)NCCN2CCCCC2)cc1)N1CCOCC1
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InChI
InChI=1S/C29H36N8O4/c1-40-29-34-25(33-27(35-29)37-17-19-41-20-18-37)21-5-9-23(10-6-21)31-28(39)32-24-11-7-22(8-12-24)26(38)30-13-16-36-14-3-2-4-15-36/h5-12H,2-4,13-20H2,1H3,(H,30,38)(H2,31,32,39)
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InChIKey
AKFJKRXXJVIFOI-UHFFFAOYSA-N
Physicochemical Property
logP
3.2435
Rotatable Bonds
9
Heavy Atom Count
41
Polar Areas
133.84
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
9
Complexity
41

"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: 56670464
ChEMBL ID
CHEMBL1808978
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: PT01045, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 = 2 nM
   TI
   LI
   LO
   TS
Protein ID: PT01029, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 = 20.5 nM
   TI
   LI
   LO
   TS
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000225 MDA-MB-361 Homo sapiens (Human)  1
1
IC50 < 31 nM
   TI
   LI
   LO
   TS