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US5049694A Expired / Lapsed US ⏱️ 0.0 years remaining

Pharmaceutical composition having relaxing activity which contains a nitrate ester as active substance

Assignee: CEDONA PHARMACEUTICALS OUDEWEG 147 2031 CC HAARLEM NETHERLANDS A Co OF NETHERLANDS BV
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Filing: 1989-09-14
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Granted: 1991-09-17
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Expires: 2009-09-14
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Abstract

Abstract The invention relates to pharmaceutical compositions containing novel nitrate esters, of which it was found that they are useful for the treatment of ischemiatic heart diseases, decompensatio cordis, myocardial infarction and hypertension.

Inventors

  • 👤 Jan Bron
  • 👤 Geert J. Sterk
  • 👤 Jan F. van der Werf
  • 👤 Hendrik Timmerman

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 06:45
CPC Classifications
C; C07; C07D; C07D493/00; C07D493/02; C07D493/04; A; A61; A61K; A61K31/00; A61K31/21; A61P; A61P9/00; A61P9/08; A61P9/10; C07C; C07C203/00; C07C203/02; C07C203/04; C07C203/08; C07C205/00; C07C205/39; C07C205/42; C07D335/00; C07D335/04; C07D335/10; C07D335/12; C07C2601/00; C07C2601/02; C07C2601/12; C07C2601/14; C07C2602/00; C07C2602/02; C07C2602/14; C07C2602/26; C07C2602/28; C07C2603/00; C07C2603/02; C07C2603/04; C07C2603/30; C07C2603/32

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 347 words
Pharmaceutical composition having relaxing activity, for example the treatment of heart and vascular diseases which contains a nitrate ester as active substance, characterized in that said ester ##STR4## , wherein R 0 represents H,OH which may be esterified by substituted or unsubstituted aliphatic or (hetero)aromatic carboxylic acid, or a group ##STR5## in which later formula R 3 represents H or a substituted or unsubstituted (hetero)aromatic group, but is possibly lacking in case X 2 represents a triple bond, R 4 represents H, OH or straight or branched alkyl, alkenyl, alkynyl or alkoxy or cyclopropyl, or is identical to R 3 , but is possibly lacking in case X 2 represents a triple bond, R 5 represents H or straight or branched alkyl, but is lacking in case X 2 represents a double or triple bond, X 1 represents a single bond, methylene, a substituted or unsubstituted carboxamide group or amino group, O or S, but is lacking in case X 2 represents a triple bond and X 2 represents a single bond, a double bond (in which case R 5 is then lacking), or a triple bond (in which case R 5 and either R 3 --X, or R 4 are then lacking), a substituted or unsubstituted carboxamide group or amino group, O or S, R 1 represents straight or branched alkylene having 1-8 carbon atoms in a straight chain, cycloalkylene having 3-7 carbon atoms, bicycloalkylene having 5-12 carbon atoms, a 1,4:3,6-dianhydrohexitrolylene group or a derivative from said group, or mono-, di- or tri-alkylene substituted cycloalkylene, R 2 represents H, OH, straight or branched alkyl or alkylphenyl, where phenyl has the same substitution possibilities as R 3 , or substituted or unsubstituted thioxanethenyl, substituted or unsubstituted benzocycloalkanyl having 5-7 carbon atoms in the cycloalkanyl chain, substituted or unsubstituted benzocycloalkenyl having 5-7 carbon atoms in the cycloalkenyl chain, substituted or unsubstituted dibenzocycloalkanyl having 5-7 carbon atoms in the cycloalkanyl chain, or substituted or unsubstituted dibenzocycloalkenyl having 5-7 carbon atoms in the cycloalkyl chain and n is 1, 2 or 3, or a salt derived from such as ester.
Claim 2
Dependent Claim 347 words
Pharmaceutical composition having relaxing activity, for example the treatment of heart and vascular diseases which contains a nitrate ester as active substance, characterized in that said ester ##STR4## , wherein R 0 represents H,OH which may be esterified by substituted or unsubstituted aliphatic or (hetero)aromatic carboxylic acid, or a group ##STR5## in which later formula R 3 represents H or a substituted or unsubstituted (hetero)aromatic group, but is possibly lacking in case X 2 represents a triple bond, R 4 represents H, OH or straight or branched alkyl, alkenyl, alkynyl or alkoxy or cyclopropyl, or is identical to R 3 , but is possibly lacking in case X 2 represents a triple bond, R 5 represents H or straight or branched alkyl, but is lacking in case X 2 represents a double or triple bond, X 1 represents a single bond, methylene, a substituted or unsubstituted carboxamide group or amino group, O or S, but is lacking in case X 2 represents a triple bond and X 2 represents a single bond, a double bond (in which case R 5 is then lacking), or a triple bond (in which case R 5 and either R 3 --X, or R 4 are then lacking), a substituted or unsubstituted carboxamide group or amino group, O or S, R 1 represents straight or branched alkylene having 1-8 carbon atoms in a straight chain, cycloalkylene having 3-7 carbon atoms, bicycloalkylene having 5-12 carbon atoms, a 1,4:3,6-dianhydrohexitrolylene group or a derivative from said group, or mono-, di- or tri-alkylene substituted cycloalkylene, R 2 represents H, OH, straight or branched alkyl or alkylphenyl, where phenyl has the same substitution possibilities as R 3 , or substituted or unsubstituted thioxanethenyl, substituted or unsubstituted benzocycloalkanyl having 5-7 carbon atoms in the cycloalkanyl chain, substituted or unsubstituted benzocycloalkenyl having 5-7 carbon atoms in the cycloalkenyl chain, substituted or unsubstituted dibenzocycloalkanyl having 5-7 carbon atoms in the cycloalkanyl chain, or substituted or unsubstituted dibenzocycloalkenyl having 5-7 carbon atoms in the cycloalkyl chain and n is 1, 2 or 3, or a salt derived from such as ester.
Claim 3
Dependent Claim 9 words
New compound, characterized ##STR6## as defined in claim 1.
Claim 4
Dependent Claim 14 words
A compound according to claim 2 which is 2-(1-naphthyl)ethanol nitrate and a salt thereof.
Claim 5
Dependent Claim 13 words
A compound according to claim 2 which is 1,4-bis(2-nitroxyethyl)benzene and a salt thereof.
Claim 6
Dependent Claim 14 words
A compound according to claim 2 which is 3,3-diphenyl-1-propanol nitrate and a salt thereof.
Claim 7
Dependent Claim 14 words
A compound according to claim 2 which is 3-phenyl-3-(4-pyridyl)-1-propanol nitrate-4-methylbenzenesulfonate and a salt thereof.
Claim 8
Dependent Claim 14 words
A compound according to claim 2 which is 3-phenoxy-1,2-propanediol dinitrate and a salt thereof.
Claim 9
Dependent Claim 15 words
A compound according to claim 2 which is 1,4-di(hydroxymethyl) cyclohexane dinitrate and a salt thereof.
Claim 10
Dependent Claim 14 words
A compound according to claim 2 which is 1,6-hexanediol dinitrate and a salt thereof.
Claim 11
Dependent Claim 15 words
A composition according to claim 1 containing, as an added ingredient, a pharmaceutically acceptable carrier.
Claim 12
Dependent Claim 40 words
A method for treating a member selected from the group consisting of ischemiatic heart diseases, decompsatio cordis, myocardial infarction, hypertension, achalasia and tardy dyskinesia which comprises administering to a subject, an effective amount of a composition according to claim 10.

References Cited (Backward Citations)

US3301891A Cited
US3428667A Cited
US3853891A Cited
US4336408A Cited
US4417903A Cited
US4479905A Cited
US4801596A Cited
US4863949A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-09-16 1995-03-18 1995-09-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-09-16 1999-03-18 1999-09-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-09-16 2003-03-18 2003-09-17 $7700.00 Window Closed / Lapsed

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