摘要:
The invention relates to novel, protected forms of Cephalosporin C and related 7-aminoadipin- amidocephalosporanic acids, their production and their use in producing corresponding 7-aminocephalosporanic acid derivatives by deacylation.
摘要:
A compound of the formula: wherein R 1 stands for hydrogen or formylamino, R 2 is a residue of amino acid or peptide selected from the group consisting of serine and alanine or hydrogen, R 3 stands for -NH-C (=NH) -NH 2 or -CH 2 NH 2 , or its salt, which can be produced by cultivating a microorganism belonging to the genus Xanthomonas, is useful as a therapeutic agent against infectious disease caused by bacteria.
摘要:
Novel cephalosporin compounds are described which are characterised by having a phenoxyacetoxymethyl group at the 3-position. The new compounds are particularly useful intermediates in the synthesis of cephalosporin antibiotics having a 3-methyl group carrying the residue of a nucleophile.
摘要:
A 7-acyl-3-substituted carbamoyloxy cephem compound represented by the following formula (1):
wherein A means a -CH= or -N= group; R¹ denotes a hydroxyl, lower alkoxyl, fluorine-substituted lower alkoxyl or protected hydroxyl group; R² and R³ are the same or different and individually represent a lower alkyl, hydroxyl-substituted lower alkyl, a carbamoyl-substituted lower alkyl group or cyano-substituted lower alkyl group, R² is a hydrogen atom and R³ is a lower alkoxyl or alkyl group optionally substituted by one or more halogen atoms, or the group
means a 4-6 membered heterocyclic group, which contains one nitrogen atom, or a morpholino group, said heterocyclic group or morpholino group being optionally substituted by one or more lower alkyl, hydroxyl and/or hydroxyl-substituted lower alkyl groups; and R⁴ denotes a carboxyl or protected carboxyl group; or a pharmaceutically acceptable salt thereof; and a process for the preparation thereof; use thereof as well as an antibacterial composition containing the above cephem compound.
摘要:
A method of producing 3-alkanoyloxymethyl-3-cephem-4-carboxylic acids, which are useful as antibiotics or as intermediates in the synthesis of antibiotics, by reacting a 3-hydroxymethyl-3-cephem-4-carboxylic acid with a saturated fatty acid anhydride in an aqueous medium in the presence of an acid-acceptor base and a 4-(tertiary amino)pyridine.
摘要:
A compound of the formula: wherein R 1 stands for hydrogen or formylamino, R 2 is a residue of amino acid or peptide selected from the group consisting of serine and alanine or hydrogen, R 3 stands for -NH-C (=NH) -NH 2 or -CH 2 NH 2 , or its salt, which can be produced by cultivating a microorganism belonging to the genus Xanthomonas, is useful as a therapeutic agent against infectious disease caused by bacteria.
摘要:
The present invention relates to cephalosporin derivatives having &bgr;-lactamase inhibitory activity. The compounds are useful in preventing or treating bacterial resistance to an antibiotic, e.g. a &bgr;-lactam antibiotic. Disclosed herein are compounds that are inhibitors of class B metallo-&bgr;-lactamases, as well as class A, C, and D serine &bgr;-lactamases. In some preferred embodiments, the compounds are 3′-thiobenzoate derivatives of a cephalosporin. Pharmaceutical compositions, methods, uses, kits and commercial packages comprising the compounds are also disclosed.
摘要:
The invention relates to novel biologically active compounds of fungi of the species Ganoderma pfeifferi DMS 13239, to methods of preparing same and to their use. From the fruit-body and mycelium of Ganoderma pfeifferi DMS 13239 extracts having an antimicrobial action and suitable as preservatives, for pharmaceutical and cosmetic preparations, as antiinfective agents and in fish-farming can be obtained. Antimicrobial active substances called ganomycines which are effective against multi-resistant germs are isolated from the extracts. The total synthesis of the ganomycines and their derivatization permits their use as antibiotics.