FIELD: medicine, pharmaceutics.
SUBSTANCE: present invention refers to a new (-)-stereoisomer of formula (I) wherein X is H, or its pharmaceutically acceptable salt which agonise GABA receptor, to a pharmaceutical composition on the basis of the presented compound, to a method for preparing the (-)-stereoisomer of formula (I) or its pharmaceutically acceptable salt, to a method for inducing or maintaining general anaesthesia, to a method for promoting pain management and to a method for promoting pain management and to a method for prototyping antiemetic activity with the use of the presented (-)-stereoisomer or its pharmaceutically acceptable salt, as well as to a new diastereoisomer (-)-2-fluoro-butyl-6-isopropylphenyl ester of carbamic acid of formula (II) wherein R1 represents a chiral amino group, and X is H.
EFFECT: preparing the pharmaceutically acceptable salt which agonise GABA receptor.
16 cl, 12 ex, 6 tbl, 4 dwg
Title | Year | Author | Number |
---|---|---|---|
THERAPEUTIC COMPOUNDS | 2008 |
|
RU2470908C2 |
PHARMACEUTICAL COMPOSITION CONTAINING WATER SOLUBLE PROPOPHOL PRODRUGS AND USES THEREOF | 2003 |
|
RU2297216C2 |
ETOMIDATE ANALOGUES WITH IMPROVED PHARMACOKINETIC AND PHARMACODYNAMIC PROPERTIES | 2009 |
|
RU2540116C2 |
ANAESTHETIC COMPOSITION | 2011 |
|
RU2574022C2 |
ETOMIDATE ANALOGUES WHICH DO NOT INHIBIT SYNTHESIS OF ADRENOCORTICOSTEROIDS | 2010 |
|
RU2559888C2 |
COMPOUNDS, METHODS FOR THEIR PREPARING, USING, PHARMACEUTICAL COMPOSITION | 2002 |
|
RU2311418C2 |
2-(2-AMINO-1,6-DIHYDRO-6-OXOPURIN-9-YL)METOXY-3-HYDROXY- 1-PROPANYL-L-VALINATE, PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, METHOD OF PREPARING THEREOF, PHARMACEUTICAL COMPOSITION AND HYDROXY AND/OR AMINO PROTECTED 2-(2- AMINO-1,6-DIHYDRO-6-OXOPYRIN-9-YL) METHOXY-3-HYDROXY-1- PROPANYL-L-VALINATE | 1995 |
|
RU2133749C1 |
PRODRUGS OF ALVOCIDIB HAVING HIGH BIOAVAILABILITY | 2016 |
|
RU2752729C2 |
METHOD OF TREATMENT BY APPLICATION OF COMBINED THERAPY | 2010 |
|
RU2543348C2 |
PARENTERAL FORMULATIONS FOR ADMINISTERING MACROLIDE ANTIBIOTICS | 2013 |
|
RU2658050C2 |
Authors
Dates
2012-12-27—Published
2008-05-08—Filed