Abstract: This invention relates to thiadiazinone derivatives which have inotropic and vasodilator activity. A specific compound of this invention is 7-acetamido-9,9a-dihydroindeno[1,2-e][1,3,4]thiadiazine-2(3H)-one.
Type:
Grant
Filed:
November 6, 1984
Date of Patent:
October 7, 1986
Assignee:
Smith Kline & French Laboratories Limited
Abstract: Flukicidal N-[4-(1-phenylethenyl)phenyl]-2-hydroxy-3,5-dihalobenzamides are prepared by reacting a halosalicylic acid with a 1-(4-aminophenyl)-1-phenylethylene in the presence of a halo condensing agent. A species of the invention is N-[4-(1-phenylethenyl)phenyl]-2-hydroxy-3,5-diiodobenzamide.
Type:
Grant
Filed:
May 7, 1984
Date of Patent:
May 6, 1986
Assignee:
SmithKline Beckman Corporation
Inventors:
Alfred W. Chow, Vassilios J. Theodorides
Abstract: Certain octapeptides, which have structures characterized by being a six unit cyclic peptide ring with a dipeptide tail which lacks a glycine unit at position 9, have potent vasopressin antagonist activity. The compounds here claimed are in general characterized by having an amino acid unit at position 4 which is other than valine. An important species of the group is [1-(.beta.-mercapto-.beta.,.beta.-cyclopentamethylenepropionic acid)-2-(O-ethyl-D-tyrosine)-4-.alpha.-aminobutyric acid-8-arginine-9-desglycine]vasopressin.
Abstract: A new cephalosporin compound, 7-D-mandelamido-3-(1-sulfomethyltetrazol-5-yl) thiomethyl-3-cephem-4-carbo xylic acid monosodium salt, having unique antibacterial activity and advantageously high stability, is disclosed. Pharmaceutical compositions comprising the new cephalosporin monosodium salt are also disclosed.
Abstract: The chemical modification of virulent Pasteurella multocida and Pasteurella haemolytica strains and preparation of live bacteria vaccines from the modified organisms for immunization of bovine, porcine and ovine animal species are disclosed.
Abstract: This invention relates to 5-(phenyl)-2(1H)-pyrazinones substituted in the 4-position of the phenyl ring by an amino or acylamino group. These compounds have inotropic activity. One specific compound is 5-(4-acetamidophenyl)-2(1H)-pyrazinone.
Type:
Grant
Filed:
June 2, 1983
Date of Patent:
December 3, 1985
Assignee:
Smith Kline & French Laboratories Ltd.
Inventors:
John C. Emmett, Robert A. Slater, Brian H. Warrington
Abstract: A novel antibiotic complex of "Vancomycin-like" antibiotics, AAD 216 complex, is produced by the cultivation of a fermentation broth containing Kibdelosporangium aridum Shearer gen. nov., sp. nov. ATCC 39323 microorganisms in an aqueous nutrient medium under submerged aerobic conditions. The AAD 216 complex and its major bioactive components; AAD 216A, AAD 216B, and AAD 216C exhibit antibiotic activity and growth promotant activity.
Type:
Grant
Filed:
July 13, 1983
Date of Patent:
October 22, 1985
Assignee:
SmithKline Beckman Corporation
Inventors:
Betty A. Bowie, David J. Newman, Marcia C. Shearer, Robert D. Sitrin, Joseph R. Valenta
Abstract: Potent DBH inhibitors having the formula: ##STR1## wherein R is --CO.sub.2 H or --CH.sub.2 NHR.sup.1 can be used to inhibit DBH activity in mammals.
Type:
Grant
Filed:
April 12, 1983
Date of Patent:
July 30, 1985
Assignee:
Smithkline Beckman Corporation
Inventors:
James S. Frazee, Carl Kaiser, Lawrence I. Kruse
Abstract: Novel aglycone and pseudo-aglycones of the AAD 216 antibiotics are prepared by partial acid hydrolysis of the AAD 216 antibiotic complex or its individual factor antibiotics. AAD 216 aglycone, AAD 216 pseudo-aglycone and AAD 216A pseudo-aglycone, AAD 216B pseudo-aglycone and AAD 216C pseudo-aglycone exhibit antibacterial activity and are useful in animal health applications.
Abstract: This invention relates to 5-(phenyl)-2(1H)-pyrazinones substituted in the 4-position of the phenyl ring by a nitro group, and to a process for their preparation. These compounds are useful intermediates in the synthesis of inotropic compounds. One specific compound is 5-(4-nitrophenyl)-2(1H)-pyrazinone.
Type:
Grant
Filed:
June 2, 1983
Date of Patent:
April 30, 1985
Assignee:
Smith Kline & French Laboratories Limited
Abstract: The chemical modification of virulent Pasteurella multocida and Pasteurella haemolytica strains and preparation of live bacteria vaccines from the modified organisms for immunization of bovine, porcine and ovine animal species are disclosed.
Abstract: Disclosed is a process of preparing blood spreads for microscopical examination wherein a smooth and homogeneous plasma layer is obtained. A combination of steps including timely fixation for the purpose of cell preservation, producing a cross-linked matrix in the plasma and performing of chemical reactions by diffusing reagents across an interface, are performed for the purpose of stabilizing both the cell shape and the smoothness and homogeneity of the plasma layer, while the fresh and still wet blood spread is immersed in a non-polar, water immisicible, solvent.
Abstract: Small cosmid cloning vectors having two antibiotic resistance markers, selected from chloramphemicol resistance, streptomycin and spectinomycin resistance and tetracycline resistance markers, at least one having a unique restriction site.
Abstract: Detoxified but still immunogenic E. coli neurotoxin is prepared by bringing E. coli neurotoxin into contact with glutaraldehyde in mild operative conditions, the reaction being stopped where no more than 90% of the neurotoxin are inactivated.The obtained detoxified neurotoxin is valuable for immunizing piglets against oedema disease.
Abstract: Process for the non-degrading preparation of polysaccharide-protein complexes from bacterial capsules; the so-obtained products which are useful as vaccines against infection by the same bacteria and method for protecting human beings against the same infection by administration of pharmaceutical composition containing the polysaccharide-protein complexes.
Abstract: The chemical modification of virulent Pasteurella multocida and Pasteurella haemolytica strains and preparation of live bacteria vaccines from the modified organisms for immunization of bovine, porcine and ovine animal species are disclosed.
Abstract: The invention relates to rotavirus vaccines for man and to methods of using them.The vaccines comprise an effective dose of bovine rotavirus which is either attenuated or inactivated.The invention comprises a method of immunizing human beings against human rotavirus infections by administering said vaccines by intramuscular, oral or nasal route; it further comprises a method of immunizing infants by boosting their mother with said vaccines prior to the birth of said infants.