Synthesis and antimicrobial activity of 7 alpha-methoxypyrimidinyl-ureidocephalosporins
- PMID: 3539123
Synthesis and antimicrobial activity of 7 alpha-methoxypyrimidinyl-ureidocephalosporins
Abstract
The synthesis of a series of 7 alpha-methoxy-7-[(R)-2-[3-[5-pyrimidinyl]ureido]-2-(4-hydroxyphenyl) acetamido]-3-cephem-4-carboxylates 2 is described. 7-[(R)-2-[3-[2-(p-Aminosulfonyl)-anilino-4-hydroxy-5-pyrimidinyl]ureido- 2-(4-hydroxyphenyl)acetamido]-7 alpha-methoxy-3-[(1-methyl-1H-tetrazol-5 -yl)thio]methyl-3-cephem-4-carboxylic acid, sodium salt (2k, UG-FA 132), has exhibited a broad range of antimicrobial activity. UG-FA 132 is highly active against Gram-positive and Gram-negative organisms, including Pseudomonas and lactamase producers, and shows potent activity against anaerobes. The high efficacy of UG-FA 132 was confirmed by in vivo experiments in mice.
Similar articles
-
[6R-[(R)-2-[3-[2-(p-Aminosulfonyl)anilino-4-hydroxy-5- pyrimidinyl]ureido]-2-(4-hydroxyphenyl)acetamido]-penicillanic acid, sodium salt (VX-VC 43), a new broad-spectrum beta-lactam antibiotic. In vitro and in vivo antibiotic activity].Arzneimittelforschung. 1985;35(1A):351-5. Arzneimittelforschung. 1985. PMID: 3838677 German.
-
Comparative in vitro activity and beta-lactamase stability of moxalactam and other selected cephalosporin antibiotics.Arzneimittelforschung. 1981;31(8):1290-5. Arzneimittelforschung. 1981. PMID: 6457607
-
A novel series of parenteral cephalosporins exhibiting potent activities against Pseudomonas aeruginosa and other Gram-negative pathogens: synthesis and structure-activity relationships.Bioorg Med Chem. 2007 Nov 1;15(21):6716-32. doi: 10.1016/j.bmc.2007.08.001. Epub 2007 Aug 9. Bioorg Med Chem. 2007. PMID: 17723304
-
Synthetic studies on beta-lactam antibiotics. Part 101. Synthesis of 7beta-[2-carboxy-2-(4-hydroxyphenyl)acetamido]-7alpha-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]-methyl]-1-oxa-1-dethia-3-cephem-4-carboxylic acid disodium salt (6059-S) and its related 1-oxacephems.J Med Chem. 1979 Jul;22(7):757-9. doi: 10.1021/jm00193a001. J Med Chem. 1979. PMID: 448673 No abstract available.
-
Cefepime: a new fourth-generation cephalosporin.Am J Hosp Pharm. 1994 Feb 15;51(4):463-77; quiz 541-2. Am J Hosp Pharm. 1994. PMID: 8017411 Review.
MeSH terms
Substances
LinkOut - more resources
Medical