General Information of the Compound
Compound ID
CP0001930
Compound Name
5-(2,6-dimorpholin-4-ylpyrimidin-4-yl)-4-(trifluoromethyl)pyridin-2-amine
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Synonyms
BKM120
Buparlisib
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Structure
Formula
C18H21F3N6O2
Molecular Weight
410.4
Canonical SMILES
Nc1cc(c(cn1)-c1cc(nc(n1)N1CCOCC1)N1CCOCC1)C(F)(F)F
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InChI
InChI=1S/C18H21F3N6O2/c19-18(20,21)13-9-15(22)23-11-12(13)14-10-16(26-1-5-28-6-2-26)25-17(24-14)27-3-7-29-8-4-27/h9-11H,1-8H2,(H2,22,23)
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InChIKey
CWHUFRVAEUJCEF-UHFFFAOYSA-N
CAS
944396-07-0
Physicochemical Property
logP
1.8128
Rotatable Bonds
3
Heavy Atom Count
29
Polar Areas
89.63
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
8
Complexity
29

"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: 16654980
SID: 26514721
ChEMBL ID
CHEMBL2017974
DrugBank ID
DB11666
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: PT07498, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000019 Rat1 Rattus norvegicus (Rat)  1
1
IC50 = 117 nM
   TI
   LI
   LO
   TS
Protein ID: PT06232, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000019 Rat1 Rattus norvegicus (Rat)  1
1
IC50 = 523 nM
   TI
   LI
   LO
   TS
Protein ID: PT02733, Serine/threonine-protein kinase mTOR
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL001055 TSC1-/- MEF Mus musculus (Mouse)  1
1
IC50 = 832 nM
   TI
   LI
   LO
   TS
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000072 A2780 Homo sapiens (Human)  2
1
EC50 = 520 nM
   TI
   LI
   LO
   TS
2
GI50 = 0.635 nM
   TI
   LI
   LO
   TS
CL000083 MCF-7 Homo sapiens (Human)  1
1
GI50 = 0.158 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( Buparlisib )
Drug Name Buparlisib
Company Novartis
Indication
Breast cancer
Phase 3
Target(s)
PI3-kinase delta (PIK3CD)
Inhibitor
PI3-kinase gamma (PIK3CG)
Inhibitor
PI3-kinase beta (PIK3CB)
Inhibitor
PI3-kinase alpha (PIK3CA)
Inhibitor