Abstract: 7-(Oxoalkyl)-1,3-dialkyl xanthines whose substituents in the 1- and 3-positions are alkyl groups of 2 to 6 carbons, cyclohexyl, alkoxyalkyl or hydroxyalkyl, such as 7-(3-oxobutyl)-1,3-di-n-butylxanthine, are effective vasodilators, having a marked activity in promoting blood flow through skeletal muscle, while at the same time exhibiting low toxicity.
Type:
Grant
Filed:
June 4, 1979
Date of Patent:
September 22, 1981
Assignee:
Johann A. Wulfing
Inventors:
Gunther Brenner, Joachim Goring, Eskendar Ali Khan, Oskar Rohte, Manfred Tauscher
Abstract: It has been found that 1,3-di-n-butyl-7-(2-oxopropyl)xanthine is a particularly effective agent for increasing oxygen partial pressure and contractility in ischaemic and skeletal muscle. Pharmaceutical compositions containing 1 to 30 mg of this agent are described.
Abstract: 7-(Oxoalkyl)-1,3-dialkyl xanthines whose substituents in the 1- and 3-positions are alkyl groups of 2 to 6 carbons, cyclohexyl, alkoxyalkyl or hydroxyalkyl, such as 7-(3-oxobutyl)-1,3-di-n-butylxanthine, are effective vasodilators, having a marked activity in promoting blood flow through skeletal muscle, while at the same time exhibiting low toxicity.
Type:
Grant
Filed:
September 19, 1978
Date of Patent:
December 30, 1980
Assignee:
Johann A. Wulfing
Inventors:
Gunther Brenner, Joachim Goring, Eskendar Ali Khan, Oskar Rohte, Manfred Tauscher
Abstract: It has been found that 1,3-di-n-butyl-7-(2-oxopropyl)xanthine is a particularly effective agent for increasing oxygen partial pressure and contractility in ischaemic and skeletal muscle. Pharmaceutical compositions containing 1 to 30 mg of this agent are described.
Abstract: The salts of N-unsubstituted, N-monosubstituted and N,N-disubstituted 7-(3-amino-2-hydroxypropyl)theophylline and 5-methylisoxazole-3-carboxylic acid are hypolipidaemic agents. The compounds, of which the 7-[3-(N-methyl-N-2-hydroxyethyl)amino-2-hydroxypropyl]-theophylline salt of 5-methylisoxazole-3-carboxylic acid is a representative embodiment, are prepared by allowing the isoxazole acid and the amine to react.
Type:
Grant
Filed:
December 8, 1976
Date of Patent:
May 30, 1978
Assignee:
Johann A. Wulfing
Inventors:
Karl Credner, Joachim Goring, Gunter Brenner, Manfred Tauscher
Abstract: A compound of the formula ##STR1## wherein R is hydrogen or methyl, n is a number from 1 to 4 and `Acyl` is nicotinoyl, 3-methylpyrazole-5-carboyl, 3-methyl-isoxazolyl-5-carboyl, 5-n-butylpyridin-2-carboyl, 2-(4-chlorophenoxy)-2-methyl-propionyl, 2-acetoxybenzoyl or theophyllinyl-7-acetyl, are useful for their effect on serum lipoids and, in particular, for treating adverse hyperlipidemic states in humans.
Type:
Grant
Filed:
April 1, 1976
Date of Patent:
November 29, 1977
Assignee:
Johann A. Wulfing
Inventors:
Karl Credner, Berthold Geisel, Gunter Brenner, Manfred Tauscher
Abstract: Novel 3,4,5-trimethoxybenzoyloxyalkyl esters of 5-n-butylpyridine-2-carboxylic acid are superior to the free acid in their ability to reduce mammalian hypertension.
Type:
Grant
Filed:
September 11, 1975
Date of Patent:
November 30, 1976
Assignee:
Johann A. Wulfing
Inventors:
Karl Credner, Berthold Geisel, Oskar Rohte, Manfred Tauscher
Abstract: This invention relates to 3-methylpyrazole-5-carboxylates, to processes for the preparation of said compounds and to pharmaceutical compositions containing said compounds.
Type:
Grant
Filed:
August 1, 1975
Date of Patent:
September 14, 1976
Assignee:
Johann A. Wulfing
Inventors:
Gunter Brenner, Karl Credner, Joachim Goring, Manfred Tauscher
Abstract: Cyclic acetals or ketals of cardioglycosides derived from k-strophanthidin or strophanthidol are more readily absorbed by the stomach and intestine than the parent cardioglycoside. The acetals are produced by reaction of the parent cardioglycoside, e.g., strophanthidindigitoxide, with an aldehyde or ketone, or the corresponding acetal or ketal, in the presence of an acid condensation catalyst, to produce the k-strophanthidin derivative optionally followed by reduction to the strophanthidiol derivative.
Type:
Grant
Filed:
June 12, 1975
Date of Patent:
August 17, 1976
Assignee:
Johann A. Wulfing Fabrik Pharmazeutischer Praparate
Abstract: Cyclic acetals or ketals of cardioglycosides derived from k-strophanthidin or strophanthidol are more readily absorbed by the stomach and intestine than the parent cardioglycoside. The acetals are produced by reaction of the parent cardioglycoside, e.g., strophanthidindigitoxide, with an aldehyde or ketone, or the corresponding acetal or ketal, in the presence of an acid condensation catalyst, to produce the k-strophanthidin derivative optionally followed by reduction to the strophanthidiol derivative.
Type:
Grant
Filed:
August 10, 1971
Date of Patent:
April 20, 1976
Assignee:
Johann A. Wulfing Fabrik Pharmazeutischer Praparate
Abstract: 1,3-BIS(.beta.-ETHYLHEXYL)-5-AMINO-5-METHYLHEXAHYDROPYRIMIDINE PYRIDINE-3-CARBOXYLATE(HEXETIDINE NICOTINATE), WHICH HAS GREATER BACTERIOSTATIC ACTIVITY AND LOWER TOXICITY IN COMPARISON WITH HEXETIDINE OR OTHER SALTS OF HEXETIDINE, IS PREPARED BY REACTING HEXETIDINE OR AN ACID ADDITION SALT THEREOF WITH NICOTINIC ACID IN AN ORGANIC SOLVENT.
Type:
Grant
Filed:
February 28, 1974
Date of Patent:
March 23, 1976
Assignee:
Johann A. Wulfing
Inventors:
Manfred Tauscher, Joachim Goring, Wolfgang Busch, Oskar Rohte