CAS: 4697-36-3; Carbenicillin

该化合物是一种半合成抗生素,属于青霉素类,主要用于治疗某些克氏阴性细菌引起的感染,其特点是能够抑制细菌细胞壁合成,这是其抗菌活动的关键机制.卡比西林对普塞多莫纳斯大肠杆菌和其他肠杆菌菌特别有效.该化合物通常以其钠盐形式施用,以提高溶性性和生物利用率.其化学结构具有乙酯环特征,这对它的抗菌特性至关重要,同时具有碳信箱状体组将其与其他青霉素区别开来.卡比西林一般是良好的,但与其他抗生素一样,它可能会在一些人中引起过敏反应.必须指出,对卡比西林的抗药性可以发展,需要谨慎使用和考虑临床环境中的易感测试.总的来说,卡比西林在治疗特定细菌感染方面,特别是在其他抗生素可能不太有效的案例中,仍然是一种宝贵的选择.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

2.2-dimethyl-5-phenyl-1,3-dioxane-4,6-dione 6-aminopenicillanic acid bis-(trimethylsilyl)acetamide carbenicillin disodium saltphenylmalonic acid L-carbenicillin D-carbenicillin

合成工艺路线路线简述

    📜Carbenicillin Disodium Salt 以 Miliq Water 作为反应溶剂,化学反应生成 羧苄西林
    参考文献:Modified Tnfalpha Molecules,Dna Encoding Such Modified Tnfalpha Molecules And Vaccines Comprising Such Modified Tnfalpha Molecules And Dna
    标题:Modified Tnfalpha Molecules,Dna Encoding Such Modified Tnfalpha Molecules And Vaccines Comprising Such Modified Tnfalpha Molecules And Dna

    海关参考信息

    专利信息


    专利号:US-12421534-B2
    优先权日:2021-11-10
    标 题 :Engineered enzymes and method for the synthesis of diverse tyrosine analogs
    发明人:ALMHJELL PATRICK J; ARNOLD FRANCES H
    权利人:CALIFORNIA INST OF TECHN
    摘要:Provided herein is an engineered tryptophan synthase β-subunit (TrpB) that catalyzes the synthesis of tyrosine, tyrosine analogs, or salts thereof. Also provided herein are methods for preparing tyrosine, tyrosine analogs, or a salt thereof using the engineered TrpB described herein.

    专利号:US-12188072-B2
    优先权日:2018-03-19
    标题 :Compositions and methods for rapid in vitro synthesis of bioconjugate vaccines in vitro via production and N-glycosylation of protein carriers in detoxified prokaryotic cell lysates
    发明人:JEWETT MICHAEL CHRISTOPHER; STARK JESSICA CAROL; DELISA MATTHEW P; JAROENTOMEECHAI THAPAKORN
    权利人:UNIV NORTHWESTERN; UNIV CORNELL
    摘要:Disclosed are methods, systems, components, and compositions for cell-free synthesis of glycosylated carrier proteins. The glycosylated carrier proteins may be utilized in vaccines, including anti-bacterial vaccines. The glycosylated carrier proteins may include a bacterial polysaccharide conjugated to a carrier, which may be utilized to generate an immune response in an immunized host against the polysaccharide conjugated to the carrier. The glycosylated carrier proteins may be synthesized in cell-free glycoprotein synthesis (CFGpS) systems using prokaryote cell lysates that are enriched in components for glycoprotein synthesis such as oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs) including OSTs and LLOs associated with synthesis of bacterial O antigens.

    专利号:US-10920229-B2
    优先权日:2014-07-16
    标 题:Method for improving heterologous synthesis of Escherichia coli into polyketides and use of same
    发明人:WANG YONG; XIONG ZHIQIANG; SONG SHUJIE; LIU QIAOXIA; WANG JIANFENG
    权利人:SHANGHAI INST BIOLOGICAL SCIENCES CAS; CAS CENTER FOR EXCELLENCE IN MOLECULAR PLANT SCIENCES
    摘要:The present invention relates to a method for improving the heterologous synthesis of a polyketide by E. coli and use thereof. The yield of the polyketide heterologously synthesized by E. coli is significantly increased by attenuating the expression of seventy-two genes, such as sucC and talB, in a host strain, wherein the highest yield increase rate can reach 60% or more. Currently, erythromycin is the most clear model compound in the study on the biosynthesis of polyketids. The production strain of the present invention enables massive accumulation of 6-deoxyerythronolide (6-dEB), an erythromycin precursor, in the fermentation process, laying the foundation for the industrial production of the heterologous synthesis of erythromycin by E. coli.

    专利号:US-11046978-B2
    优先权日:2016-03-16
    标 题:Synthesis of isoprenoids and derivatives
    发明人:GONZALEZ RAMON; CLOMBURG JAMES M; CHEONG SEOKJUNG
    权利人:UNIV RICE WILLIAM M
    摘要:This disclosure generally relates to the use of enzyme combinations or recombinant microbes comprising same to make isoprenoid precursors, isoprenoids and derivatives thereof including prenylated aromatic compounds. Novel metabolic pathways exploiting Claisen, aldol, and acyioin condensations are used instead of the natural mevalonate (MVA) pathway or 1-deoxy-d-xylulose 5-phosphate (DXP) pathways for generating isoprenoid precursors such as isopentenyl pyrophosphate (IPP), dimethylallyl pyrophosphate (DMAPP), and geranyl pyrophosphate (GPP). These pathways have the potential for better carbon and or energy efficiency than native pathways. Both decarboxylative and non-carboxylative condensations are utilized, enabling product synthesis from a number of different starting compounds. These condensation reactions serve as a platform for the synthesis of isoprenoid precursors when utilized in combination with a variety of metabolic pathways and enzymes for carbon rearrangement and the addition/removal of functional groups. Isoprenoid alcohols are key intermediary products for the production of isoprenoid precursors in these novel synthetic metabolic pathways.

    专利号:US-10925977-B2
    优先权日:2006-10-05
    标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
    发明人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S
    权利人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S; CEIL POINT LLC; UNIV TEXAS
    摘要:Novel methods of synthesis of chelator-targeting ligand conjugates, compositions comprising such conjugates, and therapeutic and diagnostic applications of such conjugates are disclosed. The compositions include chelator-targeting ligand conjugates optionally chelated to one or more metal ions. Methods of synthesizing these compositions in high purity are also presented. Also disclosed are methods of imaging, treating and diagnosing disease in a subject using these novel compositions, such as methods of imaging a tumor within a subject and methods of diagnosing myocardial ischemia.

    专利号:US-2024197774-A1
    优先权日:2021-04-16
    标 题:Synthesis of Antimicrobial PVP-coated Bismuth Nanoparticles
    发明人:LOPEZ-RIBOT JOSE; VAZQUEZ-MUNOZ ROBERTO
    权利人:UNIV TEXAS
    摘要:Described herein is a facile, fast, and economical method for the synthesis of BAL-mediated PVP-BiNPs, using basic laboratory instruments and reagents readily available in most laboratories.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献


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    合成参考文献


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    参考文献:10.3390/md9060984
    摘要:Arai M, Liu L, Fujimoto T, Setiawan A, Kobayashi M. DedA protein relates to action-mechanism of halicyclamine A, a marine spongean macrocyclic alkaloid, as an anti-dormant mycobacterial substance. Mar Drugs. 2011;9(6):984–93.
    参考文献:10.3389/fmicb.2011.00139
    摘要:Rholl DA, Papp-Wallace KM, Tomaras AP, Vasil ML, Bonomo RA, Schweizer HP. Molecular Investigations of PenA-mediated β-lactam Resistance in Burkholderia pseudomallei. Front Microbiol. 2011;2():139.
    参考文献:10.1007/s10863-011-9376-1
    摘要:Matsuno T, Yoshimune K, Yumoto I. Physiological function of soluble cytochrome c-552 from alkaliphilic Pseudomonas alcaliphila AL15-21T. Journal of Bioenergetics and Biomembranes. 2011 Jul 16;43(5):473. doi: 10.1007/s10863-011-9376-1.
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