General Information of the Compound
Compound ID
CP0519545
Compound Name
2-methyl-3-[[2-methyl-3-(trifluoromethyl)phenyl]methyl]-6-morpholin-4-ylimidazo[1,2-b]pyridazine-8-carboxamide
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Structure
Formula
C21H22F3N5O2
Molecular Weight
433.434
Canonical SMILES
Cc1nc2c(cc(nn2c1Cc1cccc(c1C)C(F)(F)F)N1CCOCC1)C(N)=O
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InChI
InChI=1S/C21H22F3N5O2/c1-12-14(4-3-5-16(12)21(22,23)24)10-17-13(2)26-20-15(19(25)30)11-18(27-29(17)20)28-6-8-31-9-7-28/h3-5,11H,6-10H2,1-2H3,(H2,25,30)
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InChIKey
LIQQLHSREQDUHL-UHFFFAOYSA-N
Physicochemical Property
logP
2.89124
Rotatable Bonds
4
Heavy Atom Count
31
Polar Areas
85.75
Hydrogen Bond Donor Count
1
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: 121426388
ChEMBL ID
CHEMBL3941289
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: PT01033, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000048 PC-3 Homo sapiens (Human)  2
1
IC50 = 501 nM
   TI
   LI
   LO
   TS
2
IC50 > 513 nM
   TI
   LI
   LO
   TS