RU98102403A - APPLICATION OF 1,4-DIHYDROPYRIDININE DERIVATIVES FOR PREVENTION AND TREATMENT OF ATHEROSCLEROTIC DEGRADATION OF ARTERIAL WALLS - Google Patents

APPLICATION OF 1,4-DIHYDROPYRIDININE DERIVATIVES FOR PREVENTION AND TREATMENT OF ATHEROSCLEROTIC DEGRADATION OF ARTERIAL WALLS

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Publication number
RU98102403A
RU98102403A RU98102403/14A RU98102403A RU98102403A RU 98102403 A RU98102403 A RU 98102403A RU 98102403/14 A RU98102403/14 A RU 98102403/14A RU 98102403 A RU98102403 A RU 98102403A RU 98102403 A RU98102403 A RU 98102403A
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RU
Russia
Prior art keywords
manufacture
medicament
use according
compound
carbon atoms
Prior art date
Application number
RU98102403/14A
Other languages
Russian (ru)
Inventor
Сартани Абрахам
Леонарди Амедео
Теста Родольфо
Original Assignee
Рекордати С.А., Кемикал энд Фармасьютикал компани
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.)
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Publication date
Application filed by Рекордати С.А., Кемикал энд Фармасьютикал компани filed Critical Рекордати С.А., Кемикал энд Фармасьютикал компани
Publication of RU98102403A publication Critical patent/RU98102403A/en

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Claims (10)

1. Применение соединения общей формулы I
Figure 00000001

где Ph обозначает фенильную группу,
Аr обозначает 2-нитрофенильную, 3-нитрофенильную, 2,3-дихлорфенильную или бензофуразан-4-ильную группу,
А обозначает разветвленную алкиленовую группу, содержащую от 3 до 6 атомов углерода,
R обозначает линейноцепочечную или разветвленную алкильную группу, включающую от 1 до 6 атомов углерода, необязательно моно замещенную алкоксигруппой, содержащей от 1 до 6 атомов углерода,
R1 обозначает атом водорода, гидроксигруппу или алкильную группу, содержащую от 1 до 4 атомов углерода, и
R2 обозначает атом водорода или метильную группу,
или соль, энантиомер, гидрат или сольват такого соединения для получения лекарственного средства для профилактики, остановки или восстановления атеросклеротической деградации стенок артерий у пациентов.
1. The use of compounds of General formula I
Figure 00000001

where Ph is a phenyl group,
Ar is a 2-nitrophenyl, 3-nitrophenyl, 2,3-dichlorophenyl or benzofurazan-4-yl group,
A denotes a branched alkylene group containing from 3 to 6 carbon atoms,
R is a linear or branched alkyl group containing from 1 to 6 carbon atoms, optionally mono-substituted with an alkoxy group containing from 1 to 6 carbon atoms,
R 1 represents a hydrogen atom, a hydroxy group or an alkyl group containing from 1 to 4 carbon atoms, and
R 2 represents a hydrogen atom or a methyl group,
or a salt, enantiomer, hydrate or solvate of such a compound for the manufacture of a medicament for the prophylaxis, arrest or restoration of atherosclerotic degradation of arterial walls in patients.
2. Применение лерканидипина, (S)-лерканидипина или (R)-лерканидипина или его соли, гидрата или сольвата для получения лекарственного средства для профилактики, остановки или восстановления атеросклеротической деградации стенок артерий у пациентов. 2. The use of lercanidipine, (S) -lercanidipine or (R) -lercanidipine or its salt, hydrate or solvate for the manufacture of a medicament for the prophylaxis, arrest or restoration of atherosclerotic degradation of artery walls in patients. 3. Применение по п.1 или 2 для получения лекарственного средства, содержащего фармацевтически приемлемый носитель. 3. The use according to claim 1 or 2 for the manufacture of a medicament containing a pharmaceutically acceptable carrier. 4. Применение по любому из предшествующих пунктов для получения лекарственного средства в форме, удобной для введения. 4. The use according to any one of the preceding paragraphs for obtaining a medicinal product in a form convenient for administration. 5. Применение по п.4 для получения лекарственного средства, содержащее 5 - 70% соединения. 5. The use according to claim 4 for the manufacture of a medicament containing 5 to 70% of the compound. 6. Применение по п.4 или 5 для получения лекарственного средства, содержащее 0,1 - 400 мг соединения в стандартной дозированной форме. 6. The use according to claim 4 or 5 for the manufacture of a medicament containing 0.1 to 400 mg of the compound in unit dosage form. 7. Применение по п.4 или 5 для получения лекарственного средства, содержащее 1 - 200 мг соединения в стандартной дозированной форме. 7. The use according to claim 4 or 5 for the manufacture of a medicament containing 1 to 200 mg of the compound in unit dosage form. 8. Применение по любому пп.1 - 3 для получения лекарственного средства в форме, приемлемой для парентерального введения. 8. The use according to any one of claims 1 to 3 for the manufacture of a medicament in a form acceptable for parenteral administration. 9. Применение по п.8 для получения лекарственного средства, содержащее 0,5 - 30% соединения. 9. The use of claim 8 to obtain a medicinal product containing 0.5 to 30% of the compound. 10. Применение по п.8 или 9 для получения лекарственного средства, содержащее 0,5 - 100 соединения в стандартной дозированной форме. 10. The use of claim 8 or 9 for the manufacture of a medicament containing 0.5 to 100 compounds in unit dosage form.
RU98102403/14A 1995-07-14 1996-06-28 APPLICATION OF 1,4-DIHYDROPYRIDININE DERIVATIVES FOR PREVENTION AND TREATMENT OF ATHEROSCLEROTIC DEGRADATION OF ARTERIAL WALLS RU98102403A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ITMI95A001513 1995-07-14

Publications (1)

Publication Number Publication Date
RU98102403A true RU98102403A (en) 2000-01-27

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2425033C2 (en) * 2005-09-16 2011-07-27 Гленмарк Фармасьютикалз Лимитед Polymorphous form of lercanidipine hydrochloride and synthesis method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2425033C2 (en) * 2005-09-16 2011-07-27 Гленмарк Фармасьютикалз Лимитед Polymorphous form of lercanidipine hydrochloride and synthesis method thereof

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