CAS: 63469-19-2; Apalcillin

该化合物是一种主要用于抗菌性特性的半合成二硝基苯丙胺抗生素,主要用于抗菌素;它属于范围更广的乙酯抗生素,其作用是抑制细菌细胞壁合成,最终导致细胞分解和死亡;阿帕西林对一系列抗乳性细菌和某些抗性细菌有效,使其在治疗各种感染方面有用;它的化学结构包括一个乙酯环,这对抗微生物活动至关重要;该物质通常通过注射进行,并因其稳定性而闻名于某些乙酯类抗生素,某些细菌产生的酶,这些细菌对青霉素具有抗药性;阿帕西林的特征是吸收,分布,新陈代谢和排泄性,影响其功效和剂量疗法;与其他抗生素一样,必须明智地使用阿帕西林来降低抗生素抗生素抗药性的风险;潜在的副作用包括过敏反应,气肠道反应和正常的制药业者之间经常使用.

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      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-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: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-2005239725-A1
      优先权日:2002-02-19
      标题:Methods for synthesis of prodrugs from 1-acyl-alkyl derivatives and compositions thereof

      专利号:US-2005070715-A1
      优先权日:2003-07-15
      标 题:Methods for synthesis of acyloxyalkyl compounds

      专利号:US-7560483-B2
      优先权日:2002-02-19
      标题 :Methods for synthesis of prodrugs from 1-acyl-alkyl derivatives and compositions thereof

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      合成参考文献


      摘要:Yakugaku Zasshi. Journal of Pharmacy., 107(592), 1987 []
      摘要:S72 | NTUPHTW | Pharmaceutically Active Substances from National Taiwan University | DOI:10.5281/zenodo.3955664
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