Abstract: Pharmaceutical compositions and a method of stimulating peripheral dopamine receptors by administering internally a nontoxic effective quantity of a benzazepine derivative to an animal. Renal vasodilator and diuretic methods are also disclosed.
Abstract: Non-pathogenic varicella-zoster virus mutants are obtained by induction and isolation of temperature-sensitive mutant strains. N-methyl-N'-nitro-N-nitrosoguanidine is employed as mutagenic agent. The obtained mutants are useful for vaccine production.
Type:
Grant
Filed:
December 29, 1975
Date of Patent:
February 15, 1977
Assignee:
Recherche et Industrie Therapeutiques (R.I.T.)
Abstract: Cephalosporins with a .alpha.-amino-(ureidophenyl)acetamido substituent at position 7 are prepared by acylation of a 7-aminocephalosporin with a derivative of .alpha.-amino-p(or m)-ureidophenylacetic acid. These compounds are antibacterial agents.
Type:
Grant
Filed:
May 7, 1973
Date of Patent:
February 8, 1977
Assignee:
SmithKline Corporation
Inventors:
John Russel Eugene Hoover, Jerry Arnold Weisbach
Abstract: A method for O-acylating the 3-hydroxymethyl group of 7-acylaminocephalosporadesic acids by reaction with an azolide and new O-acyl-7-acylaminocephalosporadesic acids in which the O-acyl group is derived from an alkoxyalkanoic acid or an amino acid.
Abstract: A method of preparing .alpha.,.beta.-epoxy ketones by reacting water-soluble .alpha.,.beta.-ethylenic ketones with sodium hypochlorite. Especially useful for preparing 3,4-epoxy-butanone.
Type:
Grant
Filed:
February 26, 1976
Date of Patent:
February 1, 1977
Assignee:
SmithKline Corporation
Inventors:
Elvin L. Anderson, Bing L. Lam, George R. Wellman
Abstract: Heterocyclic compounds which are inhibitors of histamine activity, in particular, inhibitors of H-2 histamine receptors. A specific compound of this invention is 2-[2-(4-methyl-5-imidazolylmethylthio)ethylamino]-4-pyrimidone.
Type:
Grant
Filed:
October 6, 1975
Date of Patent:
January 25, 1977
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
Graham John Durant, John Colin Emmett, Charon Robin Ganellin
Abstract: Phenoxypropanolamine derivatives are prepared. These compounds have .beta.-adrenergic stimulant activity particularly as selective bronchodilators.
Abstract: Penicillin derivative substituted at the 6 position with a (D)-[(2-amino-2-carboxy)-ethylthio]-acetamido group is obtained from Acremonium Chrysogenum new strain ATCC 20 389 or by semi-synthetic route. The product is an antibacterial agent.
Type:
Grant
Filed:
January 9, 1975
Date of Patent:
January 11, 1977
Assignee:
Recherche et Industrie Therapeutiques (R.I.T.)
Inventors:
Hugo Troonen, Piet Roelants, Bernard Boon
Abstract: The compounds are ethylene derivatives which are inhibitors of histamine activity, in particular, inhibitors of H-2 histamine receptors. A compound of this invention is 1-nitro-2-methylamino-2-[4-(3-chloro-pyridyl)butylamino]ethylene.
Type:
Grant
Filed:
November 5, 1975
Date of Patent:
January 11, 1977
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
Graham John Durant, John Colin Emmett, Charon Robin Ganellin, Hunter Douglas Prain
Abstract: The compounds are benzoyl benzofurans and benzothiophenes having pharmacological activity, in particular, coronary vasodilator activity useful for the treatment of angina pectoris and intermediates for the preparation thereof.
Abstract: Pharmaceutical compositions and methods of inhibiting H-1 and H-2 histamine receptors by administering an antihistamine and an H-2 histamine receptor inhibitor. Exemplary of the antihistamine in the compositions and methods of this invention is mepyramine and exemplary of the H-2 histamine receptor inhibitor is N-cyano-N'-methyl-N"-[2-((4-methyl-5-imidazolyl)-methylthio)ethyl]guanidin e.
Type:
Grant
Filed:
April 16, 1975
Date of Patent:
December 28, 1976
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
James Whyte Black, Michael Edward Parsons
Abstract: The compounds are guanidines, for example N-benzenesulphonyl-N'-[2-((4-methyl-5-imidazolyl)-methylthio)ethyl]guanidi ne, which are inhibitors of histamine activity.
Type:
Grant
Filed:
March 21, 1975
Date of Patent:
December 28, 1976
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
Graham John Durant, John Colin Emmett, Charon Robin Ganellin
Abstract: Novel bicyclic .beta.-lactam penicillin analogs which have antibacterial activity and intermediates for the synthesis thereof are disclosed. In particular, 3-acetyl-7-oxo-6.beta.-phenoxyacetylamino-1,3-diazabicyclo[3.2.0]heptane-2 -carboxylic acid and derivatives thereof are prepared.
Type:
Grant
Filed:
September 3, 1975
Date of Patent:
December 28, 1976
Assignee:
SmithKline Corporation
Inventors:
John G. Gleason, Kenneth G. Holden, William F. Huffman
Abstract: Novel cephalosporins with the trifluoroethylmercaptoacetamido, trifluoroethylsulfinylacetamido, and trifluoroethylsulfonylacetamido groups at position 7 are prepared. These compounds have antibacterial activity.
Abstract: Novel cephalosporins with the trifluoroethylmercaptoacetamido, trifluoroethylsulfinylacetamido, and trifluoroethylsulfonylacetamido groups at position 7 are prepared. These compounds have antibacterial activity.