FIELD: pharmacology.
SUBSTANCE: invention relates to the 5-amino-spiro[2.3]hexane-1-phosphonic acid of the following formula 
, which is a conformationally rigid analog of γ-aminobutyric acid. The invention also relates to a process for preparation of 5-amino-spiro[2.3]hexane-1-phosphonic acid.
EFFECT: compounds have a psychotropic effect.
2 cl, 2 ex
| Title | Year | Author | Number |
|---|---|---|---|
| METHOD FOR PRODUCING 5-AMINOSPIRO [2.3] HEXANE-1-CARBOXYLIC ACID | 2017 |
|
RU2659404C1 |
| SPIROCYCLIC CYCLOPROPANE AMINO ACIDS - ANALOGUES OF GAMMA-AMINOBUTYRIC ACID, WITH LIMITED CONFORMATIONAL MOBILITY AND BASED ON THEM PHARMACEUTICAL COMPOSITIONS | 2011 |
|
RU2468000C2 |
| METHOD OF PRODUCING ADAMANTYLALKYL AND ADAMANTYLOXYALKYL ETHERS OF TOSYLOXYMETHYL-PHOSPHONIC ACID | 2009 |
|
RU2450012C2 |
| METHOD FOR PRODUCING [1,2,3,4]-TETRAZINO-[5,6-e]-[1,2,3,4]-TETRAZINO-1,3,6,8-TETRAOXIDE | 2015 |
|
RU2593993C1 |
| TETRASUBSTITUTED BENZENES | 2008 |
|
RU2527177C2 |
| METHOD FOR PRODUCING COMPOUNDS, COMPOUNDS, COMPLEX METAL ORGANIC CATALYST | 2012 |
|
RU2652807C2 |
| METHOD OF PRODUCING 5-SUBSTITUTED 1,2,4-TRIAZOLE-3-CARBOXYLIC ACIDS AND DERIVATIVES THEREOF FROM UNIVERSAL PRECURSOR | 2015 |
|
RU2605414C1 |
| PHOSPHORUS-CONTAINING BETAINES WITH LIPOPHILIC OCTYL SUBSTITUENTS AT THE NITROGEN ATOM WITH BACTERICIDAL ACTIVITY | 2022 |
|
RU2794901C1 |
| INHIBITORS OF HIV INTEGRASE AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEREOF | 2002 |
|
RU2284315C2 |
| METHOD OF OBTAINING DERIVATIVES OF 7-(HETERO)ARYL-4,5,6,7-TETRAHYDRO[1,2,3]TRIAZOLO[1,5-A]PYRIDINE | 2013 |
|
RU2563254C2 |
