RU2001121019A - The use of maxonidine for the treatment of post-infarction conditions - Google Patents

The use of maxonidine for the treatment of post-infarction conditions

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Publication number
RU2001121019A
RU2001121019A RU2001121019/14A RU2001121019A RU2001121019A RU 2001121019 A RU2001121019 A RU 2001121019A RU 2001121019/14 A RU2001121019/14 A RU 2001121019/14A RU 2001121019 A RU2001121019 A RU 2001121019A RU 2001121019 A RU2001121019 A RU 2001121019A
Authority
RU
Russia
Prior art keywords
formula
physiologically acceptable
pharmaceutical compositions
acceptable acid
infarction
Prior art date
Application number
RU2001121019/14A
Other languages
Russian (ru)
Other versions
RU2261097C2 (en
Inventor
Регина Гертруда ШУМАКЕР
Original Assignee
Зольвай Фармасьютиклз Гмбх
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
Application filed by Зольвай Фармасьютиклз Гмбх filed Critical Зольвай Фармасьютиклз Гмбх
Publication of RU2001121019A publication Critical patent/RU2001121019A/en
Application granted granted Critical
Publication of RU2261097C2 publication Critical patent/RU2261097C2/en

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Claims (4)

1. Применение 4-хлор-5-[(4,5-дигидро-1Н-имидазол-2-ил)амино]-6-метокси-2-метилпиримидина формулы I1. The use of 4-chloro-5 - [(4,5-dihydro-1H-imidazol-2-yl) amino] -6-methoxy-2-methylpyrimidine of the formula I
Figure 00000001
Figure 00000001
и его физиологически приемлемых кислотно-аддитивных солей для получения фармацевтических композиций, предназначенных для лечения обусловленных инфарктом миокарда поражений сердечной мышцы.and its physiologically acceptable acid addition salts for the manufacture of pharmaceutical compositions for the treatment of heart muscle damage due to myocardial infarction.
2. Применение по п.1, отличающееся тем, что соединение формулы I по п.1 или его физиологически приемлемые кислотно-аддитивные соли используют для получения фармацевтических композиций, предназначенных для лечения обусловленных инфарктом миокарда поражений сердечной мышцы в острой стадии заболевания и/или в постинфарктном периоде.2. The use according to claim 1, characterized in that the compound of formula I according to claim 1 or its physiologically acceptable acid addition salts is used to obtain pharmaceutical compositions for the treatment of cardiac muscle damage due to myocardial infarction in the acute stage of the disease and / or post-infarction period. 3. Применение по п.2, отличающееся тем, что соединение формулы I по п.1 или его физиологически приемлемые кислотно-аддитивные соли используют для получения фармацевтических композиций, предназначенных для лечения обусловленных инфарктом миокарда поражений сердечной мышцы в хронической постинфарктной стадии.3. The use according to claim 2, characterized in that the compound of formula I according to claim 1 or its physiologically acceptable acid addition salts is used to obtain pharmaceutical compositions for treating cardiac muscle damage caused by myocardial infarction in the chronic post-infarction stage. 4. Способ получения фармацевтических композиций для лечения обусловленных инфарктом миокарда поражений сердечной мышцы, отличающийся тем, что из эффективного, способствующего процессу выздоровления и/или реабилитации функционального состояния сердечной мышцы количества соединения формулы I по п.1 или его физиологически приемлемых кислотно-аддитивных солей совместно с обычными фармацевтическими вспомогательными веществами изготавливают соответствующую лекарственную форму.4. A method of producing pharmaceutical compositions for treating cardiac muscle damage caused by myocardial infarction, characterized in that from the effective, conducive to the healing process and / or rehabilitation of the functional state of the heart muscle, the amount of the compounds of formula I according to claim 1 or its physiologically acceptable acid additive salts together with the usual pharmaceutical excipients, the corresponding dosage form is prepared.
RU2001121019/14A 1999-02-01 2000-01-28 Applying moxonidine for treatment of post-infarction states RU2261097C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19903780.9 1999-02-01
DE19903780 1999-02-01

Publications (2)

Publication Number Publication Date
RU2001121019A true RU2001121019A (en) 2003-06-10
RU2261097C2 RU2261097C2 (en) 2005-09-27

Family

ID=7895940

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2001121019/14A RU2261097C2 (en) 1999-02-01 2000-01-28 Applying moxonidine for treatment of post-infarction states

Country Status (26)

Country Link
US (1) US7041303B2 (en)
EP (1) EP1150680B1 (en)
JP (1) JP4686027B2 (en)
KR (1) KR20010092793A (en)
CN (1) CN1166363C (en)
AT (1) ATE286731T1 (en)
AU (1) AU774855B2 (en)
BR (1) BR0007894A (en)
CA (1) CA2361600C (en)
CZ (1) CZ20012615A3 (en)
DE (2) DE50009220D1 (en)
DK (1) DK1150680T3 (en)
ES (1) ES2235829T3 (en)
HK (1) HK1042650B (en)
HU (1) HUP0105210A3 (en)
IL (1) IL144621A (en)
NO (1) NO321061B1 (en)
NZ (1) NZ513869A (en)
PL (1) PL195124B1 (en)
PT (1) PT1150680E (en)
RU (1) RU2261097C2 (en)
SK (1) SK10082001A3 (en)
TR (1) TR200102221T2 (en)
UA (1) UA67822C2 (en)
WO (1) WO2000045820A1 (en)
ZA (1) ZA200105827B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102850331B (en) * 2012-09-17 2015-05-20 符爱清 4, 6-dichloro-2-methyl-5-(1-acetyl-2-imidazoline-2-yl)-aminopyrimidine preparation method
CN103483268B (en) * 2013-09-17 2015-10-14 常州大学 The preparation method of a kind of 4,6-bis-chloro-2-methyl-5-nitro pyrimidine

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3739779A1 (en) * 1987-11-24 1989-06-08 Beiersdorf Ag PHARMACEUTICAL PRAEPARATE
TR199802496T2 (en) * 1996-06-06 1999-02-22 Eli Lilly And Company Formulation for the treatment of congestive heart failure.

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