FIELD: organic chemistry, biochemistry, pharmacy. SUBSTANCE: invention describes novel derivatives of 1,2,4-triazolo[4,3- b]pyrido[3,2-d]-pyridazine of the general formula (I) where R1 means hydrogen atom or group -(CH2)m-Y where m means whole number from 0 to 4 and Y means C1-C6-alkyl, C1-C6-halogenalkyl, C1-C6--alkoxy-group, alkoxycarbonyl-group including up to 7 carbon atoms, C3-C7--cycloalkyl, norbornyl, phenylalkenyl group including up to 12 carbon atoms, phenyl group optionally substituted with one halogen atom or 4-pyridyl group; R2 means phenyl group optionally substituted with one or more halogen atoms or C1-C6-alkyl, C1-C6-alkoxy-, C3-C6-cycloalkoxy- methylenedioxy-, nitro-, di- (C1-C6-alkyl)-amino-or trifluoromethyl-groups, naphthyl or thienyl group; R3 means hydrogen or halogen atom or C1-C6-alkyl group, and its pharmaceutically acceptable salts, method of their synthesis, pharmaceutical composition and method of inhibition of activity of phosphodiesterase IV. Describing compounds can be used for treatment of inflammatory and allergic diseases. EFFECT: improved method of synthesis, valuable biochemical and medicinal properties. 10 cl, 2 tbl
Title |
Year |
Author |
Number |
DERIVATIVE OF 2-(3H)-OXAZOLONE, METHODS OF ITS SYNTHESIS, PHARMACEUTICAL COMPOSITION BASED ON THEREOF AND METHOD OF INHIBITION OF COX-2 ACTIVITY |
1997 |
- Pujg Duran Karles
- Pukhol' Nogera Ferran
- Fernandes Forner Dolors
|
RU2194043C2 |
DERIVATIVES OF 2-PHENYLPYRANE-4-ONE, PHARMACEUTICAL COMPOSITION BASED ON THEREOF AND METHOD FOR TREATMENT |
1999 |
- Krespo Krespo Ma Isabel'
- Khimenes Majorga Khuan Migel'
- Pujg Duran Karles
- Soka Puejo Lidija
|
RU2232158C2 |
DERIVATIVES OF 8-PHENYL-6,9=DIHYDRO[1,24]TRIAZOLO[3,4-i]PURINE-5-ONE, METHODS FOR THEIR PREPARING, INTERMEDIATE COMPOUNDS, PHARMACEUTICAL COMPOSITION AND TREATMENT METHOD |
2000 |
- Grasia Ferrer Khordi
- Fejksas Gras Khoan
- Pr'Eto Soto Khose Manuehl'
- Vega Noverola Armando
- Vidal' Khuan Bernat
|
RU2258705C2 |
TRICYCLIC 5,6-DIHYDRO-9H-PYRAZOLO-[3,4-C]-1,2,4-TRIAZOLO- -[4,3-A]-PYRIDINES, METHOD OF INHIBITION OF ACTIVITY OF PHOSPHODIESTERASE TYPE IV AND METHOD OF INHIBITION OF TUMOR-SPECIFIC NECROSIS FACTOR PRODUCING |
1996 |
- Allen Jakob Daplehntir
- Kelvin Kuper
|
RU2161158C2 |
CONDENSED PYRIDINE DERIVATIVES APPLICABLE AS ANTAGONISTS OF ADENOSINE RECEPTOR A
|
2005 |
- Vidal'-Khuan Bernat
- Istvud Pol Robert
- Gonsales-Rodriges Khakob
|
RU2370496C2 |
PYRIDAZINE 3(2H) DERIVATIVES AS INHIBITOR OF PHOSPHODIESTERASE 4 (PDE4), METHOD OF THEIR PREPARATION, PHARMACEUTICAL COMPOSITION AND METHOD OF TREATMENT |
2003 |
- Dal'-P'Jats Vittorio
- Dzhovannoni Marija-Paola
- Vergelli Klaudija
- Agilar-Iskerdo Nurija
|
RU2326869C2 |
NEW TRICYCLIC DERIVATIVES AS LTD4 ANTAGONISTS |
2003 |
- Puig-Duran Karlos
- Peres-Krespo Dan'El'
- Bach-Tana Khordi
- Rajder Khejmish
|
RU2330855C2 |
DERIVATIVES OF PYRIDAZINONE AND TRIAZINONE AND THEIR USING AS PHARMACEUTICAL PREPARATIONS |
2001 |
- Nagato Satosi
- Kavano Koki
- Ito Koiti
- Norimine Josikhiko
- Ueno Kokhsi
- Khanada Takakhisa
- Amino Khirojuki
- Ogo Makoto
- Khatakejama Sindzi
- Ueno Masataka
- Grum Ehntoni Dzhon
- Riverz Liann
- Smit Terens
|
RU2279428C2 |
POLYCYCLIC AGENTS FOR TREATING RESPIRATORY SYNCYTIAL VIRAL INFECTIONS |
2007 |
- Mitchel Dzheffri Piter
- Draffehn Ehlistar Dzhordzh
- Sehnford Vanessa Anna
- Bond Sajlas
- Lim Chin Ju
- Mehjes Peneloppe Anna
|
RU2486185C2 |
METHODS AND COMPOSITIONS FOR IMPROVING COGNITIVE FUNCTIONS |
2012 |
- Gallakher Mikhela
- Khaberman Rebekka
- Kokh Min Ten
|
RU2665021C2 |