Methods of treating or suppressing pervasive developmental disorders (PDDs) including; autistic disorder, Asperger's syndrome, childhood disintegrative disorder (CDD), Rett's disorder, and PDD-not otherwise specified (PDD-NOS) or attention deficit/hyperactivity disorder (ADHD) comprising administering to a subject in need thereof a therapeutically effective amount of one or more compounds as disclosed herein.

Methods of treating or suppressing pervasive developmental disorders (PDDs) including; autistic disorder, Asperger's syndrome, childhood disintegrative disorder (CDD), Rett's disorder, and PDD-not otherwise specified (PDD-NOS) or attention deficit/hyperactivity disorder (ADHD) comprising administering to a subject in need thereof a therapeutically effective amount of one or more compounds as disclosed herein.

Presented herein is a quinochalcone compound that displays strong anti-cancer properties and provides for synergistic anti-cancer activity when used in combination with interferon β (IFN-β) or interferon γ (IFN-γ). Accordingly, compositions comprising a quinochalcone compound, or a quinochalcone compound and an interferon are disclosed herein for use in treating cancer. Also presented herein, in some embodiments, are methods of using a quinochalcone compound, and compositions thereof, to treat inflammation.

Presented herein is a quinochalcone compound that displays strong anti-cancer properties and provides for synergistic anti-cancer activity when used in combination with interferon β (IFN-β) or interferon γ (IFN-γ). Accordingly, compositions comprising a quinochalcone compound, or a quinochalcone compound and an interferon are disclosed herein for use in treating cancer. Also presented herein, in some embodiments, are methods of using a quinochalcone compound, and compositions thereof, to treat inflammation.

Presented herein is a quinochalcone compound that displays strong anti-cancer properties and provides for synergistic anti-cancer activity when used in combination with interferon (IFN-) or interferon (IFN-). Accordingly, compositions comprising a quinochalcone compound, or a quinochalcone compound and an interferon are disclosed herein for use in treating cancer. Also presented herein, in some embodiments, are methods of using a quinochalcone compound, and compositions thereof, to treat inflammation.

Presented herein is a quinochalcone compound that displays strong anti-cancer properties and provides for synergistic anti-cancer activity when used in combination with interferon (IFN-) or interferon (IFN-). Accordingly, compositions comprising a quinochalcone compound, or a quinochalcone compound and an interferon are disclosed herein for use in treating cancer. Also presented herein, in some embodiments, are methods of using a quinochalcone compound, and compositions thereof, to treat inflammation.

Methods of treating or suppressing pervasive developmental disorders (PDDs) including; autistic disorder, Asperger's syndrome, childhood disintegrative disorder (CDD), Rett's disorder, and PDD-not otherwise specified (PDD-NOS) or attention deficit/hyperactivity disorder (ADHD) comprising administering to a subject in need thereof a therapeutically effective amount of one or more compounds as disclosed herein.

Methods of treating or suppressing pervasive developmental disorders (PDDs) including; autistic disorder, Asperger's syndrome, childhood disintegrative disorder (CDD), Rett's disorder, and PDD-not otherwise specified (PDD-NOS) or attention deficit/hyperactivity disorder (ADHD) comprising administering to a subject in need thereof a therapeutically effective amount of one or more compounds as disclosed herein.

The subject invention relates to improved tocopheryl quinine derivatives and tocopherol derivatives having improved pharmacokinetics in vivo that can, in some embodiments, be useful in the treatment of Lysosomal Storage Disorder, restoration of normal mitochondrial ATP production, modulation of intracellular calcium ion concentration and other treatments or therapies. The tocopheryl quinone derivatives and tocopherol derivatives have side chains that have terminally halogenated carbon atoms.

The subject invention relates to improved tocopheryl quinine derivatives and tocopherol derivatives having improved pharmacokinetics in vivo that can, in some embodiments, be useful in the treatment of Lysosomal Storage Disorder, restoration of normal mitochondrial ATP production, modulation of intracellular calcium ion concentration and other treatments or therapies. The tocopheryl quinone derivatives and tocopherol derivatives have side chains that have terminally halogenated carbon atoms.