RU2001124604A - Hypertension Medication - Google Patents

Hypertension Medication

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Publication number
RU2001124604A
RU2001124604A RU2001124604/14A RU2001124604A RU2001124604A RU 2001124604 A RU2001124604 A RU 2001124604A RU 2001124604/14 A RU2001124604/14 A RU 2001124604/14A RU 2001124604 A RU2001124604 A RU 2001124604A RU 2001124604 A RU2001124604 A RU 2001124604A
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RU
Russia
Prior art keywords
group
alkyl
phenyl
compounds according
forming
Prior art date
Application number
RU2001124604/14A
Other languages
Russian (ru)
Other versions
RU2270679C2 (en
Inventor
Мартин Р. УИЛКИНЗ
Дирк ТОРМЭЛЕН
Харальд Вальдек
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
Priority claimed from DE19906310A external-priority patent/DE19906310A1/en
Application filed by Зольвай Фармасьютиклз Гмбх filed Critical Зольвай Фармасьютиклз Гмбх
Publication of RU2001124604A publication Critical patent/RU2001124604A/en
Application granted granted Critical
Publication of RU2270679C2 publication Critical patent/RU2270679C2/en

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Claims (6)

1. Применение соединений общей формулы I1. The use of compounds of General formula I
Figure 00000001
Figure 00000001
где R 1 обозначает фенил(С 1 4 )алкильную группу, которая при необходимости может быть замещена на фенильном кольце (C 1 4 )алкилом, (С 1 4 )алкоксигруппой или галогеном, или нафтил(С 1 4 )алькильную группу, where R 1 denotes a phenyl (C 1 -C 4 ) alkyl group, which, if necessary, can be substituted on the phenyl ring by (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy or halogen, or naphthyl (C 1 - C 4 ) an alkyl group, R2 обозначает водород или группу, образующую биолабильный сложный эфир, иR 2 is hydrogen or a biolabile ester forming group, and R3 обозначает водород или группу, образующую биолабильный сложный эфир,R 3 denotes hydrogen or a group forming a biolabile ester, и физиологически приемлемых солей кислот формулы I для приготовления фармацевтических композиций, предназначенных для лечения симптоматических форм гипертензии, прежде всего таких форм симптоматической гипертензии, которые не обусловлены заболеваниями сердца, у крупных млекопитающих и у людей.and physiologically acceptable acid salts of formula I for the preparation of pharmaceutical compositions for the treatment of symptomatic forms of hypertension, especially those forms of symptomatic hypertension that are not caused by heart disease, in large mammals and humans.
2. Применение соединений по п.1, отличающееся тем, что симптоматическая гипертензия, которая не обусловлена заболеваниями сердца, представляет собой легочную гипертензию.2. The use of compounds according to claim 1, characterized in that symptomatic hypertension, which is not caused by heart disease, is pulmonary hypertension. 3. Применение соединений по п.1 или 2, где R2 и/или R3 обозначают группы, образующие биолабильный сложный эфир.3. The use of compounds according to claim 1 or 2, where R 2 and / or R 3 denote groups forming a biolabile ester. 4. Применение соединений по любому из предыдущих пунктов, где группа, образующая биолабильный сложный эфир, представляет собой С14алкильную группу, фенил- или фенилС14алкильную группу, прежде всего фенил, бензил или инданил, при необходимости замещенный на фенильном кольце C14алкилом или С14алкиленовой цепью, связывающей два соседних атома углерода, диоксоланилметильную группу, при необходимости замещенную на диоксолановом кольце C14алкилом, прежде всего (2,2-диметил-1,3-диоксолан-4-ил)метильную группу, или С14алканоилоксиметильную группу, при необходимости замещенную на оксиметильной группе С14алкилом.4. The use of compounds according to any one of the preceding paragraphs, wherein the biolabile ester forming group is a C 1 -C 4 alkyl group, a phenyl or phenyl C 1 -C 4 alkyl group, especially phenyl, benzyl or indanyl, optionally substituted on the phenyl ring C 1 -C 4 alkyl or C 1 -C 4 alkylene chain linking two adjacent carbon atoms, a dioxolanylmethyl group, optionally substituted on the dioxolane ring with C 1 -C 4 alkyl, especially (2,2-dimethyl-1 , 3-dioxolan-4-yl) methyl group, or C 1 -C 4 alkanoyloxime an ethyl group optionally substituted on the hydroxymethyl group by C 1 -C 4 alkyl. 5. Применение соединений по любому из предыдущих пунктов, отличающееся тем, что R2 обозначает группу, образующую биолабильный сложный эфир, и R3 обозначает водород.5. The use of compounds according to any one of the preceding paragraphs, characterized in that R 2 denotes a group forming a biolabile ester, and R 3 denotes hydrogen. 6. Применение соединений по п.1, отличающееся тем, что применяют (3S,2'R)-3-{1-[2'-(этоксикарбонил)-4'-фенилбутил]циклопентан-1-карбониламино}-2,3,4,5-тетрагидро-2-оксо-1Н-1-бензазепин-1-уксусную кислоту или ее физиологически приемлемые соли.6. The use of compounds according to claim 1, characterized in that the use of (3S, 2'R) -3- {1- [2 '- (ethoxycarbonyl) -4'-phenylbutyl] cyclopentane-1-carbonylamino} -2,3 , 4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic acid or its physiologically acceptable salts.
RU2001124604/15A 1999-02-16 2000-02-10 Medicinal agent for hypertension treatment RU2270679C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19906310.9 1999-02-16
DE19906310A DE19906310A1 (en) 1999-02-16 1999-02-16 Use of 3-(1-(2-aralkyl-2-carboxyethyl)-1-cyclopentanecarboxamido)-2,3,4,5-tetrahydro-2-oxo-1H-benz(b)azepine-1-acetic acid derivatives for treating hypertension

Publications (2)

Publication Number Publication Date
RU2001124604A true RU2001124604A (en) 2003-05-20
RU2270679C2 RU2270679C2 (en) 2006-02-27

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
RU2001124604/15A RU2270679C2 (en) 1999-02-16 2000-02-10 Medicinal agent for hypertension treatment

Country Status (28)

Country Link
US (1) US6482820B2 (en)
EP (1) EP1154777B1 (en)
JP (1) JP2002537258A (en)
KR (2) KR100797665B1 (en)
CN (1) CN1198619C (en)
AR (1) AR036864A1 (en)
AT (1) ATE295174T1 (en)
AU (1) AU773240C (en)
BR (1) BR0008260A (en)
CA (1) CA2362273C (en)
CZ (1) CZ301499B6 (en)
DE (2) DE19906310A1 (en)
DZ (1) DZ3014A1 (en)
ES (1) ES2238268T3 (en)
HK (1) HK1042247B (en)
HU (1) HUP0105491A3 (en)
IL (1) IL144622A (en)
NO (1) NO329588B1 (en)
NZ (1) NZ514058A (en)
PL (1) PL195283B1 (en)
PT (1) PT1154777E (en)
RU (1) RU2270679C2 (en)
SK (1) SK287254B6 (en)
TR (1) TR200102386T2 (en)
TW (1) TWI221770B (en)
UA (1) UA63032C2 (en)
WO (1) WO2000048601A1 (en)
ZA (1) ZA200105828B (en)

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ATE367815T1 (en) * 2000-10-04 2007-08-15 Astellas Pharma Inc USE OF A VASOPRESSIN ANTAGONIST SUCH AS CONIVAPTAN TO PRODUCE A MEDICATION FOR THE TREATMENT OF PULMONARY HYPERTENSION
PL367093A1 (en) * 2001-05-18 2005-02-21 Solvay Pharmaceuticals Gmbh Use of compounds with combined nep/mp-inhibitory activity in the preparation of medicaments
AP1758A (en) * 2001-09-10 2007-07-30 Tibotec Pharm Ltd Method for the preparation of hexahydro-furo [2,3-b]furan-3-ol.
IL162645A0 (en) * 2002-01-16 2005-11-20 Solvay Pharm Bv solid salts benzazepine compounds and their use inthe preparation of pharmaceuticals compounds
AR038681A1 (en) * 2002-02-14 2005-01-26 Solvay Pharm Bv ORAL FORMULATION OF SOLID SOLUTION OF A POVERLY SOLUBLE ACTIVE SUBSTANCE IN WATER
WO2004062692A1 (en) * 2003-01-13 2004-07-29 Solvay Pharmaceuticals B.V. Formulation of poorly water-soluble active substances
SA04250283B1 (en) * 2003-09-26 2008-05-26 سولفاي فارماسيتيكالز جي أم بي أتش Derivatives of amidomethy1-substituted1-(carboxyalkyl)-cyclopentylcarbonylamino-benzazepine-N-acetic acid
US7262184B2 (en) 2003-09-26 2007-08-28 Solvay Pharmaceuticals Gmbh Amidomethyl-substituted 1-(carboxyalkyl) cyclopentyl-carbonylamino-benzazepine-N-acetic acid compounds, process and intermediate products for their preparation and pharmaceutical compositions containing them
US7427611B2 (en) 2003-09-26 2008-09-23 Solvay Pharmaceuticals Gmbh Amidomethyl-substituted 1-(carboxyalkyl)-cyclopentyl-carbonylamino-benzazepine-N-acetic acid compounds, process and intermediate products for their preparation and pharmaceutical compositions containing them
US7452875B2 (en) 2003-09-26 2008-11-18 Solvay Pharmaceuticals Gmbh Amidomethyl-substituted 1-(carboxyalkyl) cyclopentyl-carbonylamino-benzazepine-N-acetic acid compounds, process and intermediate products for their preparation and pharmaceutical compositions containing them
DE602004010172T2 (en) 2003-11-18 2008-09-11 Solvay Pharmaceuticals Gmbh PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF KIDNEY FUNCTIONAL DISORDERS
US20050267072A1 (en) * 2004-05-14 2005-12-01 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions containing dually acting inhibitors of neutral endopeptidase for the treatment of sexual dysfunction
US20050267124A1 (en) * 2004-05-14 2005-12-01 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions comprising NEP-inhibitors, inhibitors of the endogenous producing system and PDEV inhibiitors
US20050288272A1 (en) * 2004-06-23 2005-12-29 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions comprising NEP-inhibitors, inhibitors of the endogenous endothelin producing system and AT1 receptor antagonists
AU2005315608B2 (en) 2004-12-15 2011-03-31 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions comprising NEP-inhibitors, inhibitors of the endogenous endothelin producing system and HMG CoA reductase inhibitors
US20060205625A1 (en) * 2005-02-18 2006-09-14 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions comprising NEP-inhibitors, inhibitors of the endogenous endothelin producing system and diuretics
US20070292503A1 (en) * 2006-06-16 2007-12-20 Gorissen Henricus R Oral pharmaceutical composition of poorly water-soluble active substance
US20070299054A1 (en) * 2006-06-22 2007-12-27 Rajesh Jain Oral pharmaceutical composition of a poorly water-soluble active agent
ES2719530T3 (en) * 2008-01-31 2019-07-11 Univ Vanderbilt Therapeutic treatment for lung conditions

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US4749688A (en) * 1986-06-20 1988-06-07 Schering Corporation Use of neutral metalloendopeptidase inhibitors in the treatment of hypertension
EP0254032A3 (en) * 1986-06-20 1990-09-05 Schering Corporation Neutral metalloendopeptidase inhibitors in the treatment of hypertension
CA1337400C (en) * 1987-06-08 1995-10-24 Norma G. Delaney Inhibitors of neutral endopeptidase
US5362727A (en) * 1993-07-26 1994-11-08 Bristol-Myers Squibb Substituted azepino[2,1-a]isoquinoline compounds
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