RU96121791A - APPLICATION OF Xanthine derivatives to reduce the pathological hyperactivity of eosinophilic granulocytes, new xanthine derivatives and a method for their preparation - Google Patents

APPLICATION OF Xanthine derivatives to reduce the pathological hyperactivity of eosinophilic granulocytes, new xanthine derivatives and a method for their preparation

Info

Publication number
RU96121791A
RU96121791A RU96121791/14A RU96121791A RU96121791A RU 96121791 A RU96121791 A RU 96121791A RU 96121791/14 A RU96121791/14 A RU 96121791/14A RU 96121791 A RU96121791 A RU 96121791A RU 96121791 A RU96121791 A RU 96121791A
Authority
RU
Russia
Prior art keywords
xanthine derivatives
methyl
general formula
hydrogen atom
ethyl
Prior art date
Application number
RU96121791/14A
Other languages
Russian (ru)
Other versions
RU2159617C2 (en
Inventor
Геберт Ульрих
Анагностопулос Хиристо
Крегель Клаус
Капп Александер
Original Assignee
Хехст АГ
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE4411660A external-priority patent/DE4411660A1/en
Application filed by Хехст АГ filed Critical Хехст АГ
Publication of RU96121791A publication Critical patent/RU96121791A/en
Application granted granted Critical
Publication of RU2159617C2 publication Critical patent/RU2159617C2/en

Links

Claims (5)

1. Фармацевтическая композиция, обладающая уменьшающей патологическую гиперактивность эозинофильных гранулоцитов активностью, содержащая активное вещество на основе производных ксантина и по меньшей мере одну целевую добавку, отличающаяся тем, что в качестве активного вещества она содержит по меньшей мере одно соединение общей формулы (I)
Figure 00000001

где R1 - метил или этил,
R2 - алкил с 1 - 4 атомами углерода,
X - атом водорода или гидроксил,
n - целое число от 1 до 5,
и/или его стереоизомер и/или его физиологически переносимую соль в эффективном количестве.
1. A pharmaceutical composition having activity reducing eosinophilic granulocyte pathological hyperactivity, containing an active substance based on xanthine derivatives and at least one target additive, characterized in that it contains at least one compound of the general formula (I) as an active substance
Figure 00000001

where R 1 is methyl or ethyl,
R 2 is alkyl with 1 to 4 carbon atoms,
X is a hydrogen atom or hydroxyl,
n is an integer from 1 to 5,
and / or its stereoisomer and / or its physiologically tolerated salt in an effective amount.
2. Производные ксантина общей формулы (I)
Figure 00000002

где R1 - метил или этил,
R2 - алкил с 1 - 4 атомами углерода,
X - атом водорода или гидроксил,
n - целое число от 1 до 5,
причем соединение, у которого и R1 и R2 означают метил, X - означает атом водорода и n означает число 4, исключено,
его стереоизомер и физиологические переносимые соли.
2. Xanthine derivatives of the general formula (I)
Figure 00000002

where R 1 is methyl or ethyl,
R 2 is alkyl with 1 to 4 carbon atoms,
X is a hydrogen atom or hydroxyl,
n is an integer from 1 to 5,
moreover, a compound in which both R 1 and R 2 mean methyl, X - means a hydrogen atom and n means the number 4, excluded,
its stereoisomer and physiological tolerated salts.
3. Производные ксантина общей формулы (I) по п. 1, у которых R2 означает метил или этил.3. Xanthine derivatives of the general formula (I) according to claim 1, wherein R 2 is methyl or ethyl. 4. Производные ксантина общей формулы (I) по п.1, у которых остаток X означает атом водорода. 4. Xanthine derivatives of the general formula (I) according to claim 1, in which the remainder X is a hydrogen atom. 5. Производные ксантина общей формулы (I) по п.1, у которых R1 метил,
R2 - метил или этил,
X - атом водорода,
n - целое число от 1 до 5.
5. Xanthine derivatives of the general formula (I) according to claim 1, wherein R 1 is methyl,
R 2 is methyl or ethyl,
X is a hydrogen atom,
n is an integer from 1 to 5.
RU96121791/14A 1994-04-05 1995-03-21 Xanthine derivatives, their stereoisomers and physiologically tolerable salts, pharmaceutical composition diminishing pathologic hyperactivity of eosinophilic granulates RU2159617C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4411660.8 1994-04-05
DE4411660A DE4411660A1 (en) 1994-04-05 1994-04-05 Use of xanthine derivatives to reduce the pathological hyperreactivity of eosinophilic granulocytes, new xanthine compounds and processes for their preparation

Publications (2)

Publication Number Publication Date
RU96121791A true RU96121791A (en) 1999-02-10
RU2159617C2 RU2159617C2 (en) 2000-11-27

Family

ID=6514636

Family Applications (1)

Application Number Title Priority Date Filing Date
RU96121791/14A RU2159617C2 (en) 1994-04-05 1995-03-21 Xanthine derivatives, their stereoisomers and physiologically tolerable salts, pharmaceutical composition diminishing pathologic hyperactivity of eosinophilic granulates

Country Status (11)

Country Link
EP (1) EP0758239A1 (en)
JP (1) JPH09510983A (en)
KR (1) KR100373948B1 (en)
CN (1) CN1098686C (en)
AU (1) AU695488B2 (en)
CA (1) CA2187081A1 (en)
DE (1) DE4411660A1 (en)
HU (1) HUT74732A (en)
RU (1) RU2159617C2 (en)
UA (1) UA39136C2 (en)
WO (1) WO1995026727A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6294350B1 (en) 1997-06-05 2001-09-25 Dalhousie University Methods for treating fibroproliferative diseases
US5985592A (en) * 1997-06-05 1999-11-16 Dalhousie University Uses for pentoxifylline or functional derivatives/metabolites thereof
AU3370099A (en) * 1998-03-31 1999-10-18 Mayo Foundation For Medical Education And Research Use of platelet activating factor (paf) inhibitors to inhibit il-5 induced eosinophil activation or degranulation
CN101538224A (en) 2002-05-31 2009-09-23 先灵公司 Process for preparing xanthine phosphodiesterase V inhibitors and precursers thereof
EP1719772A1 (en) * 2002-05-31 2006-11-08 Schering Corporation Process for preparing xanthine phosphodiesterase v inhibitors and precursors thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8918297D0 (en) * 1989-08-10 1989-09-20 Beecham Group Plc Novel treatment
DD298051A5 (en) * 1989-08-16 1992-02-06 ��@���������@�������k�� PROCESS FOR THE PREPARATION OF A THERAPEUTIC AGENT FOR THE TREATMENT OF DIGESTIVE DISEASES
GB9023783D0 (en) * 1990-11-01 1990-12-12 Celltech Ltd Pharmaceutical product
IL100195A0 (en) * 1990-11-30 1992-08-18 Hoechst Roussel Pharma Use of xanthines for the preparation of a medicament having immuno suppressing activity
WO1993003728A1 (en) * 1991-08-27 1993-03-04 Temple University Of The Commonwealth System Of Xanthine suppression of antigen activation of t- or b-cells
IL99368A (en) * 1991-09-02 1996-01-19 Teva Pharma Compositions for topical treatment of psoriasis and atopic dermatitis comprising a xanthine derivative
US5473070A (en) * 1992-11-16 1995-12-05 Cell Therapeutics, Inc. Substituted long chain alcohol xanthine compounds

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