General Information of the Compound
Compound ID
CP0177298
Compound Name
8-[(1R)-1-(3,5-difluorophenoxy)ethyl]-N,N-dimethyl-2-morpholin-4-yl-4-oxochromene-6-carboxamide
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Structure
Formula
C24H24F2N2O5
Molecular Weight
458.461
Canonical SMILES
C[C@@H](Oc1cc(F)cc(F)c1)c1cc(cc2c1oc(cc2=O)N1CCOCC1)C(=O)N(C)C
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InChI
InChI=1S/C24H24F2N2O5/c1-14(32-18-11-16(25)10-17(26)12-18)19-8-15(24(30)27(2)3)9-20-21(29)13-22(33-23(19)20)28-4-6-31-7-5-28/h8-14H,4-7H2,1-3H3/t14-/m1/s1
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InChIKey
WKBARHXLSQPDRQ-CQSZACIVSA-N
Physicochemical Property
logP
3.7496
Rotatable Bonds
5
Heavy Atom Count
33
Polar Areas
72.22
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
6
Complexity
33

"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: 118730717
ChEMBL ID
CHEMBL3408275
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
CL000218 BT-474 Homo sapiens (Human)  1
1
IC50 = 7400 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 970 nM
Protein ID: PT01033, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000196 MDA-MB-468 Homo sapiens (Human)  1
1
IC50 = 132 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 17 nM