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比阿培南的合成

Synthesis of Biapenem
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摘要 自从第一个碳青霉烯(carbapenem)类抗生素被应用于临床,具有化学稳定、对肾脱氢肽酶稳定和改善体内动态的1β—甲基碳青霉烯的研究就广泛开展起来。比阿培南(biapenem)由日本 Lederle 公司研制并于2001年上市,经临床应用证明对各种细菌感染治疗效果优良,毒副反应少。 The study of 1βmethylcarbapenem was warming up extensively from the first an- tibiotic of arbapenem was used to clinic.Because it has the ability of chemical stability and the sta- bility to kidney dehydrogenase,and it can also improve the dynmic condition of our body.Beapen- em was developed by Lederle company of Japan,and was trown—into the market in 2001.Clinical application proves that the therapy result is good,and the toxic reaction or the side reaction is Iit- tle.
作者 徐秀杰
出处 《黑龙江医药》 CAS 2004年第6期444-446,共3页 Heilongjiang Medicine journal
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参考文献4

  • 1United States Patent 4,925,836.
  • 2β-Lactams. 3. Asymmetric Total Synthesis of New NonNatural 1 β-Methyl-carbapenems Exhibiting Strong Antimicobial Activities and Stalility against Human Renal Dehydropeptidase- I. Yaohimitsu Nagao, Yunosuke Nagase, et al.J. Org. Chem. 1992,57,4243.
  • 3New Straightforward Synthesis and Characterization of a Unique 1α-Methyl-carbapenems Antibiotic Biapenem Bearing a б-Symmetric Bicyclotriazoliumtyil Group as the Pendant Moiety. Toshio Kumagai, Satoshi Tamai,et AL. J. Org. Chem.1998,63,8145.
  • 4United States Patent 5,948,785.

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