FIELD: medicine, organic chemistry. SUBSTANCE: invention proposes a novel agent with immunomodulating effect. Agent comprises selective agonist with affinity constant to CB2 receptor by at least 30 times lower than affinity constant to CB1 receptor. As such agonist the known or novel compounds can be used of general formulas (I) 
or (I') 
with radical values given in the invention claim. Except for immunomodulating effect, some compounds exhibit analgetic effect additionally. EFFECT: expanded arsenal of agents of prescription claimed. 13 cl, 1 test, 7 tbl, 11 sch, 13 ex
| Title |
Year |
Author |
Number |
| DERIVATIVES OF N-SULFONYL-2-OXOINDOLE, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS AND PHARMACEUTICAL COMPOSITION CONTAINING AGENT THAT SHOWS ACTIVITY WITH RESPECT TO VASOPRESSIN AND/OR OXYTOCIN RECEPTORS |
1993 |
- Lois Fulon
- Zhorzh Gareia
- Dino Nizato
- Rishar Ru
- Klodin Serradejl'-Legal'
- Zherar Valett
- Zhan Van'On
|
RU2135469C1 |
| INDOLINE DERIVATIVES, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS, PHARMACEUTICAL COMPOSITION |
1992 |
- Zhan Van'On[Fr]
- Klod Pluzan[Fr]
- Klodin Serradej-Legal'[Fr]
- Dino Nizato[It]
- Bernar Tonner[Fr]
|
RU2104268C1 |
| DERIVATIVES OF N-(1,5-DIPHELYL-1H-PYRAZOL-3-YL)SULPHONAMIDE WITH AFFINITY TO CB RECEPTORS |
2005 |
- Bart Fransis
- Konzhi Kristian
- Martines Serzh
- Rinal'Di-Karmona Mjuriehll'
|
RU2366657C2 |
| SUBSTITUTED 1-PHENYL-3-CARBOXAMIDES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF SHOWING AFFINITY TO HUMAN NEUROTENSIN RECEPTORS |
1996 |
- Labejuv Bernar
- Gjulli Daniell'
- Zhanzhan Fransis
- Molimar Zhan-Sharl'
- Buazhegrehn Rober
|
RU2195455C2 |
| SUBSTITUTED HETEROCYCLIC COMPOUNDS, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION |
1996 |
- Ksav'E Ehmon-Al'T
- Izabell' Grossrieter
- Patrik Gel'
- Vinchentso Proietto
- Did'E Van Bruk
|
RU2157807C2 |
| N-TRIAZOLYL-2-INDOLECARBOXAMIDES, METHOD OF THEIR SYNTHESIS (VARIANTS), PHARMACEUTICAL COMPOSITION CONTAINING THEREOF (VARIANTS) AND 1-SUBSTITUTED 3-AMINOTRIAZOLES |
1998 |
- Bin'On Ehrik
- Bra Zhan-P'Er
- De Kuante Pol'
- Desperu P'Er
- Frel' Daniel'
- Gjulli Daniel'
|
RU2175323C2 |
| 1-PHENYLALKYL-1,2,3,6-TETRAHYDROPYRIDINES, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF |
1997 |
- Baroni Marko
- Kardamone Rozanna
- Furn'E Zhaklin
- Gutstsi Umberto
|
RU2189975C2 |
| TRIAZOLIUM SALT AS RAR1 INHIBITORS, PREPARING THEM AND USING AS DRUG PREPARATION |
2009 |
- Khajnel'T Uve
- Vener Fol'Kmar
- Kherrmann Mattias
- Shenafinger Karl
- Shtajnkhagen Khenning
|
RU2494100C2 |
| AMINES FOR PREPARING MEDICINAL AGENTS DESIGNATED FOR PROPHYLAXIS OF TUMOR CELLS PROLIFERATION |
1997 |
- Brel'Er Zhan-Klod
- Ferrara Paskual'
- Lebuteje Kristin
- Pol' Rajmon
- Rozenfel'D Khorkhe
- Van Bruk Did'E
|
RU2176502C2 |
| DERIVATIVES OF PYRAZOLE, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION CONTAINING THEREOF AND INTERMEDIATE COMPOUNDS OF SYNTHESIS |
1993 |
- Fransi Bart
- P'Er Kazella
- Kristian Konzhi
- Serzh Martinez
- Mjur'Ell' Rinal'Di
|
RU2119917C1 |
