FIELD: organic chemistry, pharmacy. SUBSTANCE: invention describes novel immunofylline- specific ligands of the general formula (I) where R1 is residue of amino acid methyl ester taken among ε-NH2- lysine, ε-lysine, phenylalanine; R2 is hydrogen atom; R is butylhydroxycarbonyl, carboxybenzyl, residue of 4-piperidine carboxylic acid, 2-indoline carboxylic acid; R4 is hydrogen atom; A is aromatic group; β-D is -CH = C-; X is O; Y is C. They show antiasthmatic and immunodepressant effect and can be used as the parent compounds for synthesis of medicinal agents. Invention describes also method of their synthesis, pharmaceutically ready form, medicinal agent and method of its preparing. EFFECT: new compounds indicated above, improved method of synthesis, valuable medicinal properties. 19 cl, 3 tbl, 13 ex
Title |
Year |
Author |
Number |
ANTAGONISTS OF LUTEINIZING HORMONE RELEASING-FACTOR (VARIANTS), METHOD OF THEIR SYNTHESIS (VARIANTS), PHARMACEUTICAL COMPOSITION AND METHOD OF MEDICINAL PREPARATIONS PREPARING |
1996 |
- Bekers Tomas
- Bernd Mikhaehl'
- Klenner Tomas
- Kucher Berngard
- Sharpent'E Parisil-Mari
- Ehmig Peter-Paul'
|
RU2163910C2 |
DRUG FOR TREATMENT OF PATIENT WITH VIRAL INFECTIONS, AIDS AND/OR AIDS-ASSOCIATED COMPLEX (VARIANTS), PEPTIDE OR ITS PHARMACEUTICALLY ACCEPTABLE SALT (VARIANTS) AND NONA- AND DECAPEPTIDES AS DRUGS FOR TREATMENT OF PATIENT WITH VIRAL INFECTIONS, AIDS AND/OR AIDS-ASSOCIATED COMPLEX |
1994 |
- Ehngel' Jurgen
- Kutcher Bernkhard
- Bernd Mikhaehl'
- Nimajer Ul'F
|
RU2154492C2 |
PYRIDO[3,2-E]PYRAZINONES, METHODS OF PREPARATION THEREOF, PREPARATION BASED ON THESE COMPOUNDS, AND METHOD OF THEIR PREPARATION |
1996 |
- Khefgen Norbert
- Bjukhner Tomas
- Akhterrat-Tukermann Ute
- Zelenyj Shtefan
- Kucher Berngard
|
RU2143433C1 |
PHOSPHOLIPID DERIVATIVES, A METHOD OF THEIR SYNTHESIS, A PHARMACEUTICAL COMPOSITION BASED ON SAID, METHODS OF A PHARMACEUTICAL COMPOSITION PREPARING |
1993 |
- Gerkhard Nessner
- Jurij Shtekar
- Peter Khilgard
- Bernkhard Kucher
- Jurgen Ehngel
|
RU2126413C1 |
METHOD OF PREPARING FREE RUNNING 6,8-THIOCTIC ACID, 6,8-THIOCTIC ACID |
1996 |
- Khorst Betge
- Kurt Klostermann
- Roland Meller
- Gerkhard Zator
|
RU2159240C2 |
ANALOGS OF LHRH ANTAGONISTS AND METHODS OF THEIR SYNTHESIS |
1991 |
|
RU2123499C1 |
N-SUBSTITUTED INDOLE-3-GLYOXYLAMIDES AND MEDICINAL PREPARATION ELICITING ANTI-ASTHMATIC, ANTI-ALLERGIC AND IMMUNODEPRESSIVE/IMMUNOMODULATING EFFECT, METHOD FOR PREPARING COMPOUNDS (VARIANTS) AND METHOD FOR PREPARING MEDICINAL PREPARATION |
1997 |
- Bruneh Kaj
- Zelenyj Shtefan
- Kucher Berngard
- Lebo Gijom
- Mens'Ju Sesilija
- Ehmig Peter
|
RU2237661C2 |
DERIVATIVES OF 1-(2-OXOACETYL)-PIPERIDINE- OR PYRROLIDINE-2-CARBOXYLIC ACIDS, PHARMACEUTICAL COMPOSITION, METHOD OF TREATMENT, METHOD OF SYNTHESIS |
1993 |
- Dehvid M. Armistid
- Dzheffri O. Saunders
- Dzhoshua S. Boger
|
RU2158258C2 |
METHOD OF PRODUCING 5-SUBSTITUTED 1,2,4-TRIAZOLE-3-CARBOXYLIC ACIDS AND DERIVATIVES THEREOF FROM UNIVERSAL PRECURSOR |
2015 |
- Matveev Andrej Valerevich
- Prutkov Aleksandr Nikolaevich
- Chudinov Mikhail Vasilevich
|
RU2605414C1 |
SLIGHTLY SOLUBLE RELEASING HORMONE-LUTEONIZING HORMONE ANALOG SALT, SLIGHTLY SOLUBLE BOMBESINE ANALOG SALT, PHARMACEUTICAL COMPOSITION, MEDICINAL PREPARATION |
1994 |
- Ehngel' Jurgen
- Klokkers-Betke Karin
- Rejssman Tomas
- Khil'Gard Peter
|
RU2152222C1 |