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: 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 1, 1976
Date of Patent:
January 10, 1978
Assignee:
SmithKline Corporation
Inventors:
John Russel Eugene Hoover, Jerry Arnold Weisbach
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 1, 1976
Date of Patent:
January 10, 1978
Assignee:
SmithKline Corporation
Inventors:
John Russel Eugene Hoover, Jerry Arnold Weisbach
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 1, 1976
Date of Patent:
January 10, 1978
Assignee:
SmithKline Corporation
Inventors:
John Russel Eugene Hoover, Jerry Arnold Weisbach
Abstract: New semisynthetic cephalosporins are described whose structures are characterized by having an .alpha.-oxyimino group in the 7-acetamido moiety and a sulfosubstituted tetrazolylthiomethyl group at position 3. The compounds are active antibacterial agents especially against Gram negative organisms.
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 anti-bacterial activity.
Abstract: New semisynthetic cephalosporins characterized by having structures with a 1-dihydroxypropyltetrazole-5-ylthiomethyl group at position 3. Exemplary is the antibacterially effective 7-D-mandelamido-3-[1-(2,3-dihyroxypropyl)tetrazole-5-ylthiomethyl]-3-cephe m-4-carboxylic and 7-(D-.alpha.-phenyl-.alpha.-aminoacetamido)-3-[1-(2,3-dihydroxypropyl)-tet razole-5-ylthiomethyl]-3-cephem-4-carboxylic acid.
Abstract: A device for smearing liquid on a slide has (1) a housing and means for supporting a pair of slides on top of the housing, (2) a carriage with a pair of spaced runners which slidably support the carriage on the top of the housing, (3) a spreader pivotally mounted on the carriage and free to rock transversely with respect to a slide, (4) a member to advance the carriage and spreader, (5) a spring and dashpot arrangement to retract the carriage, and (6) latch means to arrest the carriage after it retracts a short distance. The means for supporting the slides may support the slide at an angle of at least five degrees with respect to the plane in which the carriage moves reducing the thickness of the liquid smeared on the slide. The dashpot plunger moves in the direction of an open end of the dashpot cylinder. Advantageously the device has means to clean the spreader.
Abstract: The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a substituted triazolyl thiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.
Abstract: 7.beta.-Substituted mercaptoacetamido-7.alpha.-methoxycephalosporanic acid and derivatives thereof are prepared. These compounds are antibacterial agents with improved properties.
Abstract: The uriedoalkyl substituted tetrazolethiol compounds of this invention are used for preparing 7-acyl-3-(uriedoalkyl substituted tetrazolythiomethyl)-cephalosporins.
Abstract: Pharmaceutical compositions having direct acting skeletal muscle relaxant activity comprising .alpha.,.alpha.-diphenyl-3-tropidineethanol and methods of producing skeletal muscle relaxant activity by administering internally said compositions.
Abstract: Pharmaceutical compositions having antiarthritic activity comprising phosphine or phosphite bis-coordinated gold(1+) salts and methods of producing antiarthritic activity by administering internally, preferably orally, said compositions.
Abstract: A new process for preparing 2,3-dichloroanisole comprises reacting 1,2,3-trichlorobenzene with an alkali metal methoxide preferably in the presence of methanol.
Abstract: New semisynthetic cephalosporins characterized by having structures with a 1-carboxymethylthioethyltetrazolyl-5-thiomethyl group at position 3. Exemplary is the antibacterially effective 7-D-mandelamido-3-(1-carboxymethylthioethyltetrazolyl-5-thiomethyl)-3-ceph em-4-carboxylic acid disodium salt.
Abstract: Lower alkyl 4-imidazolecarboxylates are electro-chemically reduced to give the corresponding alcohol and lower alkyl ethers. This mixture is reacted directly with cysteamine to give the important thioamine intermediates.
Abstract: The improved live Newcastle disease virus vaccines of the invention contain a cold or cold and temperature-sensitive strain of Newcastle disease virus obtained by U.V. or nitrous acid mutation. The vaccines are administered to chickens in the form of an aerosol.
Abstract: A process for preparing 7-oxo cephalosporins and 6-oxo penicillins by reaction of a 7-amino cephalosporin or 6-amino penicillin with a carbonyl-containing oxidizing agent is disclosed.