Abstract: Pharmaceutical compositions having antiarthritic activity comprising Bis[(Trialkylphosphine)Gold(I)]Sulfides and methods of producing antiarthritic activity by administering internally, preferably orally, said compositions.
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 anti-bacterial activity.
Abstract: A Reimer-Tiemann reaction of 2,3-dichlorophenol with carbon tetrachloride gives 2,3-dichloro-4-hydroxy-benzoic acid, a novel intermediate, which is then reacted with thiophene in the presence of phosphorus pentoxide or polyphosphoric acid to give 2,3-dichloro-4-(2-thienoyl)-phenol. This compound is then converted to the diuretic, ticrynafen, by known prior art reactions.
Abstract: A multiple dose paste dispenser has a frame with a handle secured thereto. A piston rod having a piston on the front end is mounted in said frame for longitudinal movement. A cartridge is secured to the frame in alignment with the piston. A gripping ring is slidable along said rod and grippably engages the rod when it is tilted with respect to the rod. A return spring urges the ring in a direction away from the piston. A trigger pivotally mounted on the frame is adapted to tilt the ring and advance the ring, the rod and the piston into the cartridge. A stop is pivoted to the frame for movement from an inoperative position to a position for limiting the advance of the ring. Advantageously the stop is stepped to provide for at least two different stop positions.
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:
October 10, 1976
Date of Patent:
May 23, 1978
Assignee:
SmithKline Corporation
Inventors:
John Russel Eugene Hoover, Jerry Arnold Weisbach
Abstract: A new series of 7-acylamino-8-oxo-3-oxa-1-azabicyclo-[4.2.0]octane-2-carboxylic acid derivatives is described which compounds have antibacterial activity especially against certain Gram negative organisms.
Type:
Grant
Filed:
September 8, 1976
Date of Patent:
May 16, 1978
Assignee:
SmithKline Corporation
Inventors:
Thomas Francis Buckley, John Gerald Gleason
Abstract: Tricyclic quinolizidine derivatives administered internally to an animal host, in therapeutically effective amounts, produce antipsychotic activity essentially free of extrapyramidal symptoms.
Abstract: Tricyclic piperidylidene derivatives administered internally to an animal host, in therapeutically effective amounts, produce antipsychotic activity without extrapyramidal symptoms. Certain of the active ingredients are novel compounds per se.
Abstract: A method for dephthaloylation of azetidinone compounds which contain a phthalimido group to produce useful aminoazetidinone intermediates comprises reaction with methyl hydrazine at low temperatures.
Abstract: New semisynthetic cephalosporins characterized by having structures with a 3-sulfomethyl-1,2,4-triazol-5-ylthiomethyl group at position 3. Exemplary is the antibacterially effective 7-D-mandelamido-3-(3-sulfomethyl-1,2,4-triazol-5-ylthiomethyl)-3-cephem-4- carboxylic acid disodium salt.
Abstract: Substituted aurones useful as inhibitors of certain antigen-antibody reactions, particularly in alleviating allergic manifestations such as asthma, are prepared by reaction of a 3-coumaranone with an appropriately substituted benzaldehyde followed by treatment with aqueous mineral acid and an alkanol.
Abstract: An improvement in the decyanation of tertiary nitriles comprises the alkali fusion of the nitriles. Exemplary are the preparation of chlorpheniramine and brompheniramine by heating the respective nitriles in liquid sodium or potassium hydroxide at from 100.degree.-200.degree..
Abstract: New semisynthetic cephalosporins characterized by having structures with a 5-sulfomethyl-1,3,4-thiadiazol-2-ylthiomethyl group at position 3. Exemplary is the anti-bacterially effective 7-D-mandelamido-3-(5-sulfomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem -4-carboxylic acid disodium salt.
Abstract: Uricosuric compositions containing 2,3-dichloro-4-carboxyphenoxyacetic acid or its alkali metal salts and methods of producing uricosuria and hypouricemia by administering said compounds.
Abstract: Novel cephalosporins with the trifluoroethylmercaptoacetamido, trifluoroethylsulfinylacetamido, and trifluoroethylsulfonylacetamido groups at position 7 are prepared. These compounds have antibacterial activity.
Abstract: Novel piperidylidene derivatives of benzo-fused xanthenes, thioxanthenes and dibenzoxepins administered internally to an animal host, in therapeutically effective amounts, produce antipsychotic activity essentially free of extrapyramidal symptoms.
Abstract: The stereospecific cycloaddition of nitrogen containing acetic acid halides or anhydrides with Schiff bases having a carbalkoxy group substituted on the methine carbon atom offers new intermediates and methods for preparing synthetic cephalosporin congeners having antibacterial activity.
Type:
Grant
Filed:
June 14, 1976
Date of Patent:
February 7, 1978
Assignee:
SmithKline Corporation
Inventors:
John G. Gleason, Kenneth G. Holden, William F. Huffman
Abstract: A new method of preparing trifluoromethylthioacetic acid using a tertiary phosphine in a sulfur extrusion of lower alkyl trifluoromethyldithioacetate with optional is situ alkaline hydrolysis of said acetate using a biphasic hydrolysis system in the presence of a phase transfer catalyst.
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.