Abstract: A new process is disclosed for the preparation of N-acyl-.alpha.-aromatic and N-acyl-.alpha.-heteroaromatic glycines by reaction of an .alpha.-ester or ether of an N-acylglycine ester or acid with an aromatic or heteroaromatic compound. Also disclosed are new intermediates for preparing N-acyl-.alpha.-aromatic and N-acyl-.alpha.-heteroaromatic glycines.
Type:
Grant
Filed:
October 3, 1975
Date of Patent:
December 14, 1976
Assignee:
SmithKline Corporation
Inventors:
John G. Gleason, Kenneth G. Holden, Nelson C. F. Yim
Abstract: A series of 3-alkylamino-.alpha.-substituted aminomethyl-4-hydroxybenzyl alcohols are prepared. These compounds are .beta.-adrenergic stimulants, in particular as bronchodilators.
Abstract: A new process is disclosed for the preparation of N-acyl-.alpha.-aromatic and N-acyl-.alpha.-heteroaromatic glycines by reaction of an .alpha.-ester or ether of an N-acylglycine ester or acid with an aromatic or heteroaromatic compound. Also disclosed are new intermediates for preparing N-acyl-.alpha.-aromatic and N-acyl-.alpha.-heteroaromatic glycines.
Type:
Grant
Filed:
June 24, 1975
Date of Patent:
November 30, 1976
Assignee:
SmithKline Corporation
Inventors:
John G. Gleason, Kenneth G. Holden, Nelson C. F. Yim
Abstract: Cephalosporin compounds with 3-substituted ureido or -thioureido group at position 7 and hydrogen or heterocyclicthiomethyl groups at position 3 are prepared. These compounds are antibacterial agents.
Type:
Grant
Filed:
June 3, 1975
Date of Patent:
November 30, 1976
Assignee:
Recherche et Industrie Therapeutiques (R.I.T.)
Abstract: Cephalosporin compounds with 3-substituted ureido or -thioureido group at position 7 and hydrogen or heterocyclicthiomethyl groups at position 3 are prepared. These compounds are antibacterial agents.
Type:
Grant
Filed:
June 4, 1975
Date of Patent:
November 30, 1976
Assignee:
Recherche et Industrie Therapeutiques (R.I.T.)
Abstract: Novel folic acid derivatives useful for radio-assaying folic acid and its metabolites in biological liquids are prepared from pteroyl-.gamma.-glutamyl-tyrosines by iodination with I.sup.125 or I.sup.131.
Abstract: Uricosuric compositions containing 2,3-dichloro-4-(.alpha.-hydroxy-2-thenyl)phenoxyacetic acid, its alkali metal salts or pharmaceutically acceptable base addition salts and methods of producing uricosuria and hypouricemia by administering said compounds. Either the racemic mixture or a separated d-or l-optical isomer may be employed as the active ingredient.
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-[.alpha.-Amino-.alpha. -(acylamidophenyl)acetamido]-cephalosporins are prepared. They show improved antibacterial activity especially when they are administered orally.
Abstract: .beta.-Naphthylmethyl piperazinyl derivates having anti-Parkinsonism activity prepared by condensation of .beta.-chloromethylnaphthalene with the appropriate substituted piperazine.
Abstract: 7-(p-Hydroxymethylphenylglycylamido)cephalosporins are prepared by acylating a 7-aminocephalosporin compound. The products have antibacterial activity.
Abstract: Cephalosporin compounds substituted at the 7-position with free or substituted .alpha.-amino or hydroxy phenylacetamido and at the 3-position with a heterocyclic thiomethyl group are prepared by displacement of a 3-acetoxymethyl compound with a mercaptoheterocycle or by 7-acylation. The products are antibacterial agents.
Abstract: 3-Substituted-3-hydroxyphenyl-2-piperidylcarbinols are prepared. These compounds are .beta.-adrenergic stimulants and are useful in particular as bronchodilators.
Abstract: Pharmaceutical compositions comprising tetramic acid analogs of pulvinic acid and methods of combating arthritis by administration of these compositions are disclosed.
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.
Abstract: Pharmaceutical compositions and methods of inhibiting gastric acid secretion by administering 1-(9-xanthenyl) amino-substituted-piperidines and pyrrolidines and new 1-(9-xanthenyl) amino-piperidine compounds.