RU94033356A - NEW TETRAHYDRONAPTALINE DERIVATIVES, METHOD FOR THEIR PRODUCTION, PHARMACEUTICAL COMPOSITION ON THEIR BASIS AND METHOD FOR ITS PRODUCTION - Google Patents
NEW TETRAHYDRONAPTALINE DERIVATIVES, METHOD FOR THEIR PRODUCTION, PHARMACEUTICAL COMPOSITION ON THEIR BASIS AND METHOD FOR ITS PRODUCTIONInfo
- Publication number
- RU94033356A RU94033356A RU94033356/04A RU94033356A RU94033356A RU 94033356 A RU94033356 A RU 94033356A RU 94033356/04 A RU94033356/04 A RU 94033356/04A RU 94033356 A RU94033356 A RU 94033356A RU 94033356 A RU94033356 A RU 94033356A
- Authority
- RU
- Russia
- Prior art keywords
- production
- derivatives
- new
- tetrahydronaptaline
- basis
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 230000000875 corresponding Effects 0.000 claims 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 2
- 241000124008 Mammalia Species 0.000 claims 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N Tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 230000000767 anti-ulcer Effects 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
Claims (1)
где R<M^ >1<D> - атом водорода; R<M^>2<D> - атом водорода, C<Mv>1<D> - С<Mv>4<D> - алкоксикарбонилалкильная или бензильная группа (R<M^>1<D> и R<M^ >2<D> вместе образуют группу, описываемую формулой -(СН<Mv>2<D>)<Mv>3<D>-); R<M^ >3<D> - гидроксильная, C<Mv>1<D> - С<Mv>4<D>-алкокси- или бензилокси-группа, отвечающая общей формуле
в которой R<M^>5<D> обозначает C<Mv>1<D> - С<Mv>4<D>-алкильную группу, а n равно О, 1, 2, 3 или 4, а также их фармацевтически приемлемых солей и способа их получения. Предлагаемые соединения проявляют существенную противоязвенную активность у млекопитающих, включая человека.The invention relates to new derivatives of tetrahydronaphthalene, corresponding to the General formula I
where R <M ^> 1 <D> is a hydrogen atom; R <M ^> 2 <D> is a hydrogen atom, C <Mv> 1 <D> - C <Mv> 4 <D> is an alkoxycarbonylalkyl or benzyl group (R <M ^> 1 <D> and R <M ^ > 2 <D> together form a group described by the formula - (CH <Mv> 2 <D>) <Mv> 3 <D>-); R <M ^> 3 <D> is a hydroxyl, C <Mv> 1 <D> - C <Mv> 4 <D> alkoxy or benzyloxy group, corresponding to the general formula
in which R <M ^> 5 <D> denotes C <Mv> 1 <D> is a C <Mv> 4 <D> is an alkyl group, and n is O, 1, 2, 3 or 4, as well as their pharmaceutically acceptable salts and methods for their preparation. The proposed compounds exhibit significant anti-ulcer activity in mammals, including humans.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU4021/91 | 1991-12-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU94033356A true RU94033356A (en) | 1996-03-20 |
Family
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