摘要:
The compounds are 6-(2-amino-hexahydro-2-indancarboxamido) penicillanic acids and 6-(1,2,3,4,5,6,7,8,9,10decahydronaphthalene-2-amino-2-carboxamido) pencillanic acids, which have broad spectrum antimicrobial activity against both gram-positive and gram-negative strains of bacteria, including penicillin-resistant staphylococci. The compounds are also characterized by being relatively acid-resistant, thereby to be effective on oral administration, and by low water solubility which makes them useful in repository injectable dosage forms without the necessity for forming salts thereof with organic bases.
摘要:
The present invention provides a method for selective delivery of a therapeutic or diagnostic agent to a targeted organ or tissue by implanting a biocompatible solid support in the patient being linked to a first binding agent, and administering a second binding agent to the patient linked to the therapeutic or diagnostic agent, such that the therapeutic or diagnostic agent accumulates at the targeted organ or tissue.
摘要:
Derivatives of anacardic acid having antimicrobial properties and method for preparing said derivatives. The antimicrobial properties include bacteriostatic and bacteriocidal activity.
摘要:
THIS INVENTION IS CONCERNED WITH NEW AND NOVEL PARTIALLY DEHYDRATED AND ANHYDROUS 6-(1-AMINOCYCLOALKYLCARBOXAMIDO)PENICILLANIC ACIDS AND PROCESSES FOR THE PREPARATION THEREOF.
摘要:
The present invention provides a method for selective delivery of a therapeutic or diagnostic agent to a targeted organ or tissue by implanting a biocompatible solid support in the patient being linked to a first binding agent, and administering a second binding agent to the patient linked to the therapeutic or diagnostic agent, such that the therapeutic or diagnostic agent accumulates at the targeted organ or tissue.
摘要:
Derivatives of anacardic acid having antimicrobial properties and method for preparing said derivatives. The antimicrobial properties include bacteriostatic and bacteriocidal activity.
摘要:
An enzymatic process for the preparation of aminocyclohexylpenicillin is disclosed. The process involves reacting together 6-aminopenicillanic acid or other penicillins and aminocyclohexyl carboxylic acid, or esters and/or acid addition salts thereof in the presence of an enzyme elaborated by such microorganisms as are found in the genera Pseudomonas, Kluyvera, Escherichia, Aerobacter, Micrococcus, Streptomyces, Nocardia, Aspergillus or Penicillium.