Aza-substituted psilocin analogs and methods of synthesizing the same
The present invention is directed to novel chemical compositions of matter and their methods of synthesis, and in particular novel analogs of Psilocin having enhanced physical and pharmacokinetic characteristics.
1 . A psilocin analog compound comprising:
wherein
X 1 is N, or NH;
X 2 is CH;
X 3 is CH;
A is C;
R 1 is O, or —OH;
R 2 is linear alkane-R 3 , wherein R 3 is (CH3) 2 NH (dimethylamine); and wherein said dashed lines represents possible double bond positions according to the configuration of X being N or CH, and R 1 being O or —OH; or
a pharmaceutically acceptable salt thereof.
2 . The compound of claim 1 , wherein said compound is:
a pharmaceutically acceptable salt thereof.
3 . The compound of claim 1 , further comprising at least one pharmaceutically acceptable carrier, forming a pharmaceutical composition.
4 . The compound of claim 2 , further comprising at least one pharmaceutically acceptable carrier, forming a pharmaceutical composition.
5 . A psilocin analog compound comprising:
wherein
X 1 is N, or NH;
X 2 is CH;
X 3 is CH;
A is C;
R 1 is O, or —OH;
R 2 is linear alkane-R 3 , wherein R 3 is (CH3CH(CH3)NHCH(CH3)CH3 (diisopropylamine);
and wherein said dashed lines represents possible double bond positions according to the configuration of X being N or CH, and R 1 being O or —OH; or
a pharmaceutically acceptable salt thereof.
6 . The compound of claim 5 , further comprising at least one pharmaceutically acceptable carrier, forming a pharmaceutical composition.