Abstract: Pharmaceutical compositions and method of producing anti-Parkinsonism activity by administering internally a nontoxic effective quantity of a benzazepine derivative to an animal.
Type:
Grant
Filed:
August 5, 1975
Date of Patent:
October 4, 1977
Assignee:
SmithKline Corporation
Inventors:
Carl Kaiser, Robert G. Pendleton, Paulette E. Setler
Abstract: A liquid fraction collector has a first series of containers and a second series of containers, each of the first and second series of containers being arranged in a plurality of groups with means to support each group at a different elevation. A conduit leads upwardly from each container in said first series with the upper ends of the conduits lying in a first row and a conduit leads upwardly from each container in said second series with the upper end of the conduits lying in a second row parallel to the first row. A carriage is mounted above said conduits. The carriage has means to discharge a liquid having an inverted V guide member with one trough over one row and the other trough over the other row and a discharge tube having its discharge end movable from a position over one trough of the guide member to a position over the other trough of the guide member.
Type:
Grant
Filed:
December 22, 1975
Date of Patent:
September 20, 1977
Assignee:
SmithKline Corporation
Inventors:
David J. Cooper, George W. Gebhardt, Joseph R. Valenta, Francis E. Wdzieczkowski
Abstract: A process for preparing 5-(alkoxy- and aminoethylthio)methylthiazole compounds via displacement of the trisubstituted phosphonium group from 5-(trisubstituted phosphonium)methylthiazole compounds is disclosed.
Type:
Grant
Filed:
October 29, 1975
Date of Patent:
September 20, 1977
Assignee:
SmithKline Corporation
Inventors:
Bing Lun Lam, Joseph James Lewis, Robert Lee Webb, George Robert Wellman
Abstract: The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a sulfonic acid or sulfamoyl substituted tetrazolyl thiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.
Abstract: .alpha.-Aminomethyl-4-hydroxy-3-methylsulfonyl benzyl alcohols having .beta.-adrenergic antagonist activity are prepared generally from 4-benzyloxy-3-methylsulfonylacetophenone by, for example, bromination and treatment of the resulting .alpha.-bromo derivative with an N-benzyl secondary amine, followed by catalytic hydrogenation to remove protective benzyl groups and reduce the ketone moiety.
Abstract: Novel pseudodisaccharide compounds which are related to neamine are prepared. These compounds have a mercapto group or a derivative thereof at position 3 or 4 of the glucose moiety of neamine. The compounds have antibacterial activity and have utility as intermediates to pseudotrisaccharides.
Type:
Grant
Filed:
December 18, 1975
Date of Patent:
September 13, 1977
Assignee:
SmithKline Corporation
Inventors:
David J. Cooper, John R. E. Hoover, Jerry A. Weisbach
Abstract: Cephalosporia compounds having a substituted phenylglycyl substituent at the 7-position and any of a variety of groups at the 3-position are prepared by acylation of a 7-aminocephalosporanic acid. The compounds have anti-bacterial activity.
Abstract: The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a sulfoalkyl substituted oxadiazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.
Abstract: The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a carboxyalkyl or carbamoylalkyl substituted oxadiazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.
Abstract: Aromatic prostaglandin derivatives are prepared. These compounds have valuable antiprostaglandin activity specifically inhibiting prostaglandin synthesis and antagonizing diarrhea induced by prostaglandin E.sub.2 (PGE.sub.2).
Type:
Grant
Filed:
November 21, 1975
Date of Patent:
June 28, 1977
Assignee:
SmithKline Corporation
Inventors:
William G. Groves, Bernard Loev, Carl D. Perchonock
Abstract: Substituted 2H-pyran-2,6(3H)-dione derivatives, pharmaceutical compositions comprising such derivatives and methods of inhibiting the antigen-antibody reaction by administering said compositions. The active ingredients are the products formed by the reaction of acetonedicarboxylic acid with acetic anhydride followed by reaction with an appropriate amine. Certain of the dione derivatives are novel compounds per se.
Type:
Grant
Filed:
April 30, 1976
Date of Patent:
June 28, 1977
Assignee:
SmithKline Corporation
Inventors:
Lawrence W. Chakrin, Kenneth M. Snader, Chester R. Willis
Abstract: Methods and intermediates are disclosed for the preparation of trifluoromethylthioacetic acid using the reaction of trifluoromethylsulfenyl halides with certain orthoesters.
Type:
Grant
Filed:
April 15, 1976
Date of Patent:
June 7, 1977
Assignee:
SmithKline Corporation
Inventors:
Sidney Harry Levinson, Wilford Lee Mendelson
Abstract: A process for purifying semisynthetic cephalosporins is disclosed which uses alumina and/or a polymeric nonionic resin as adsorbents at a controlled pH. The process is more efficient than previously used methods.
Abstract: The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and an ureidoalkyl substituted tetrazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.
Abstract: Substituted 2H-pyran-2,6(3H)-dione derivatives useful in the treatment of allergic conditions are prepared by reaction of 3,5-diacetyl-4,6-dihydroxy-2H-pyran-2-one with an appropriate aniline.
Abstract: New anthelmintic compositions and methods of use are described utilizing 5-cycloalkylthio and oxy-2-carbalkoxyaminobenzimidazoles as active ingredients.
Abstract: Substituted 2H-pyran-2,6(3H)-dione derivatives useful in the treatment of allergic conditions are prepared by reaction of 3,5-diacetyl-4,6-dihydroxy-2H-pyran-2-one with an appropriate aniline.
Abstract: N,N'-Bis[2-(3-substituted-4-hydroxyphenyl)-ethyl or -2-hydroxyethyl]-polymethylenediamines having .beta.-adrenergic stimulant activity particularly as selective bronchodilators, are prepared generally by condensation of an N-benzylphenethylamine with a polymethylene dihalide or by reaction of an .beta.-bromoacetophenone with an N,N'-dibenzyl-polymethylenediamine, with further operations depending on the nature of the 3-substituent, and subsequently hydrogenating catalytically with for example palladium-on-carbon. The key intermediates are also part of the invention.
Abstract: The compounds of this invention are substituted benzofurans and benzothiophenes having pharmacological activity. In particular, these compounds have coronary vasodilator activity and are useful in the treatment of angina pectoris.
Type:
Grant
Filed:
November 17, 1975
Date of Patent:
May 17, 1977
Assignee:
SmithKline Corporation
Inventors:
L. Martin Brenner, John M. Petta, Stephen T. Ross
Abstract: Cephalosporin compounds having a substituted phenylglycyl substituent at the 7-position and any of a variety of groups at the 3-position are prepared by acylation of a 7-aminocephalosporanic acid. The compounds have antibacterial activity.