CAS: 84880-03-5; Cefpimizole

该化合物是一种合成抗生素,属于甲状腺素类,其特点是乙状乳腺结构,主要用于抗菌性特性,对一系列抗菌性细菌和克状阴性细菌有效,Cefpimizole通过抑制细菌细胞壁合成,导致细胞分解和死亡而开展的工作,该化合物通常通过注射进行,并因其稳定性而闻名于某些乙状乳腺,这些乙状腺是某些细菌为抵抗抗生素行动而生成的酶,其药用植物遗传学包括良好的组织渗透和相对较短的半衰期,需要多剂量才能有效治疗,常见副作用可能包括胃肠紊乱,过敏反应和对肾功能的潜在影响.与其他抗生素一样,抗力的出现是一个关切问题,突出了在临床环境中适当使用的重要性.总体来说,丙皮质素是防止细菌感染的一件有价值的选择,特别是在其他抗生素可能无效的情况下.

结构式图片

MSDS等安全信息

    合成工艺路线路线简述

      📜Ajicef 反应生成 头孢咪唑
      参考文献:Sajto,Xidehtomi;Yamamoto,Rinya;Nomura,Mayuki;Yatani,Gukehj
      标题:Sajto,Xidehtomi;Yamamoto,Rinya;Nomura,Mayuki;Yatani,Gukehj

      海关参考信息

      专利信息


      专利号:US-8017776-B2
      优先权日:2003-07-15
      标题 :Methods for synthesis of acyloxyalkyl compounds
      发明人:BHAT LAXMINARAYAN; GALLOP MARK A
      权利人:XENOPORT INC
      摘要:Disclosed herein are methods for synthesizing 1-(acyloxy)-alkyl prodrug derivatives of drugs through oxidation of 1-acyl-alkyl derivatives of drugs under anhydrous reaction conditions. The methods typically proceed stereospecifically, in high yield, do not require the use of activated intermediates and/or toxic compounds and are readily amenable to scale-up.

      专利号:US-9693999-B2
      优先权日:2011-01-26
      标题:Small molecule RNase inhibitors and methods of use
      发明人:DUNMAN PAUL M; OLSON PATRICK D; CHILDERS WAYNE
      权利人:UNIV ROCHESTER; UNIV NEBRASKA; Temple University—Of the Commonwealth System of Higher Education
      摘要:Small molecule inhibitors of bacterial ribonuclease (e.g., RnpA) and methods for their synthesis and use are described herein. The methods of using the compounds include treating and preventing microbial infections and inhibiting bacterial ribonuclease. Also described herein are methods of identifying compounds for treating or preventing a microbial infection.

      专利号:US-8143437-B2
      优先权日:2002-02-19
      标题:Methods for synthesis of prodrugs from 1-acyl-alkyl derivatives and compositions thereof
      发明人:GALLOP MARK A; XIANG JIA-NING; YAO FENMEI; BHAT LAXMINARAYAN; ZHOU CINDY X
      权利人:GALLOP MARK A; XIANG JIA-NING; YAO FENMEI; BHAT LAXMINARAYAN; ZHOU CINDY X; XENOPORT INC
      摘要:The present invention provides a method for synthesizing 1-(acyloxy)-alkyl derivatives from 1-acyl-alkyl derivatives, which typically proceeds stereospecifically, in high yield, does not require the use of activated intermediates and/or toxic compounds and is readily amendable to scale-up. The current invention also provides 1-acyl-alkyl derivatives of known drug components and methods for synthesizing these 1-acyl-alkyl derivatives.

      专利号:US-2009111737-A1
      优先权日:1999-05-24
      标题:Novel antibacterial agents
      发明人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
      权利人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
      摘要:This invention relates to novel multibinding compounds (agents) that are antibacterial agents. The multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands in their monovalent (i.e., unlinked) state have the ability to bind to a an enzyme involved in cell wall biosynthesis and metabolism, a precursor used in the synthesis of the bacterial cell wall and/or the bacterial cell surface thereby interfere with the synthesis and/or metabolism of the cell wall. In particular the multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands hasn a ligand domain capable of binding to penicillin binding proteins, a transpeptidase enzyme, a substrate of a transpeptidase enzyme, a beta-lactamase enzyme, pencillinase enzyme, cephalosporinase enzyme, a transglycoslase enzyme, or a transglycosylase enzyme substrate; Preferably, the ligands are selected from the beta lactam or glycopeptide class of antibacterial agents.

      专利号:WO-2009056955-A1
      优先权日:2007-10-30
      标题 :Amine-bearing phospholipids (abps), their synthesis and use
      发明人:ZUMBUEHL ANDREAS
      权利人:UNIV BASEL; ZUMBUEHL ANDREAS
      摘要:Disclosed herein are amine-bearing phospholipids (ABP). The ABPs display many properties and functionalities of naturally occurring phospholipids, but also new properties and functionalities, such as the ability to polymerize while maintaining structural integrity, that may supplement or expand the functionalities of naturally occurring phospholipids.

      专利号:US-9868747-B2
      优先权日:2014-02-18
      标题:Marinopyrrole derivatives and methods of making and using same
      发明人:LI RONGSHI; SEBTI SAID; LIU YAN; QIN YONG; SONG HAO; CHENG CHUNWEI
      权利人:H LEE MOFFITT CANCER CT & RES; CHONGQING ZEIN PHARMACEUTICAL CO LTD
      摘要:Marinopyrrole derivatives and methods for their synthesis and use are described herein. Novel cyclic and symmetric marinopyrroles with triazole substituents having antibacterial activity against resistant bacterial strains, such as MRSA are introduced. Also provided are methods of using the compounds for treating or preventing cancer and/or microbial infections.

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      📌 第三方产品分析报告

      ✅ COA系统入驻 | 共享模式

      主要参考文献


      1: Xu H, Xu R, Wang X, Liang Q, Zhang L, Liu J, Wei J, Lu Y, Yu D. Co-infections of Aeromonas veronii and Nocardia seriolae in largemouth bass (Micropterus salmoides). Microb Pathog. 2022 Dec;173(Pt A):105815. doi: 10.1016/j.micpath.2022.105815. Epub 2022 Oct 7. 10(2):91-6. doi: 10.1179/joc.1998.10.2.91. 107(5):225-35. Japanese. doi: 10.1254/fpj.107.225. 40(5):333-8. doi: 10.1111/j.1348-0421.1996.tb01076.x. 14(5):877-85. doi: 10.1016/0192-0561(92)90087-2. 80(4):619-20. Japanese. 34(6):1160-4. doi: 10.1128/AAC.34.6.1160.
      8: Oishi K, Matsumoto K, Yamamoto M, Morito T, Yoshida T. Stimulatory effect of cefodizime on macrophage-mediated phagocytosis. J Antibiot (Tokyo). 1989 Jun;42(6):989-92. doi: 10.7164/antibiotics.42.989. 15(2):73-7. doi: 10.1097/00007435-198804000-00001. 63(1):19-25. Japanese. 31(12):1904-8. doi: 10.1128/AAC.31.12.1904.
      12: Novak E, Lakings DB, Paxton LM. Tolerance and disposition of cefpimizole in normal human volunteers after intramuscular administration. Antimicrob Agents Chemother. 1987 Nov;31(11):1706-10. doi: 10.1128/AAC.31.11.1706.

      合成参考文献


      摘要:S6 | ITNANTIBIOTIC | Antibiotic List from the ITN MSCA ANSWER | DOI:10.5281/zenodo.2621956
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