| Title |
Year |
Author |
Number |
| USE OF IMIDAZOLE DERIVATIVES FOR PREPARING PHARMACEUTICAL COMPOSITION SHOWING ACTIVITY TO ANGIOTENSIN RECEPTORS AT AND AT, SOME OF THESE COMPOUNDS, METHOD OF SYNTHESIS OF IMIDAZOLE DERIVATIVES AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF |
1995 |
- Alan Korb'E
- P'Er Depre
- Mishel' Fortehn
- Zhak Gijom
- Bertran Ehkman
|
RU2141321C1 |
| DERIVATIVES OF IMIDAZOLE, METHODS OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS AND PHARMACEUTICAL COMPOSITION BASED ON IMIDAZOLE DERIVATIVES |
1995 |
- Ehkmann Bertran
- Vever Zhan Pol'
- Zang Zhidong
|
RU2187507C2 |
| DERIVATIVES OF IMIDAZOLE, METHODS OF THEIR SYNTHESIS, INTERMEDIATE SUBSTANCES AND PHARMACEUTICAL COMPOSITIONS BASED ON IMIDAZOLE DERIVATIVES |
1995 |
- Bertran Ehkmann
- Zhan-Pol' Vever
- Zhidong Zang
|
RU2171257C2 |
| BICYCLIC IMIDAZOLE DERIVATIVES AND METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUND AND METHOD OF ITS SYNTHESIS, PHARMACEUTICAL COMPOSITION |
1994 |
- Alen Korb'E
- Zhan Pol' Vever
- Zhidong Zkhang
|
RU2141481C1 |
| METHOD FOR PREPARING SULFUR-CONTAINING IMIDAZOLE DERIVATIVES AND INTERMEDIATE PRODUCTS |
1993 |
- Neerzha Bkhatnagar
- Zhan Bjuandia
- Kristin Grifful'
- Khol'Ger Khajch
- Adal'Bert Vagner
|
RU2135475C1 |
| SULFUR-CONTAINING DERIVATIVES WITH RETROAMIDE LINKAGE AS INHIBITORS OF ENDOTHELIN-CONVERTING ENZYMES |
1997 |
- Depre P'Er
- Djuma Zhak
- Gijom Zhak
|
RU2215526C2 |
| DERIVATIVES OF BENZOPYRANE-2-ONE, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION COMPRISING THEREOF AND INTERMEDIATE COMPOUNDS |
1997 |
- Klish Mishel'
- Loren Patrik
- Musitskij Branislav
- Shio Loran
|
RU2194052C2 |
| SULFUR-CONTAINING IMIDAZOLE DERIVATIVES, METHOD OF THEIR SYNTHESIS, NEW INTERMEDIATE COMPOUNDS AND PHARMACEUTICAL COMPOSITION |
1991 |
- Zhan-Klod Kaj[Fr]
- Alehn Korb'E[Fr]
- Mishel' Fortehn[Fr]
- Zhil' Amon[Fr]
- Simon Zhukej[Fr]
- Zhan-Pol' Vever[Fr]
|
RU2086542C1 |
| NEW DERIVATIVES OF ERYTHROMYCIN, METHOD FOR THEIR PREPARING AND USING AS DRUGS |
1999 |
|
RU2237672C2 |
| IMIDAZOLE DERIVATIVES, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION DECREASING BLOOD PRESSURE |
1992 |
- Al'Bert Vagner[De]
- Khajnrikh Ehnglert[De]
- Khajnts-Verner Kleemann[De]
- Khermann Gerkhards[De]
- Bernvard Shel'Kens[De]
- Rajnkhard Beker[De]
- Vol'Fgang Lints[De]
|
RU2104272C1 |
where R1 is alkyl or alkylthio-group; R2 is C1-C8-alkylthio-group possibly substituted with one or some halogen atoms or radical -CO-Z where Z is a free carboxyl radical or that converted to salt or ester; R3 is radical 
where X means oxygen atom or radical of the formula (a) 
(radicals D1,D2 and R5 have values given in p. 1 of the invention claim) and also their acid addition salts. Synthesized compounds show antagonistic properties to receptors of angiotensin-II, in part, they inhibit vasoconstrictive effect and trophic effect at the level of myocytes. Invention describes 3 methods of synthesis of compounds of the formula (I), pharmaceutical composition and intermediate compounds. EFFECT: new compounds indicated above, improved method of synthesis, valuable pharmacological properties. 11 cl, 66 ex