CAS: 37661-08-8; Bacampicillin Hydrochloride

该化合物是丙烯菊酯的一种杀菌剂,目的是通过改善胃肠道的吸收,提高口服生物利用率.作为半合成乙酯-林丹抗生素,在活性丙酰胺体内进行水解,以释放活性丙烯,提供抗丙烯丙烯的广谱抗菌活动,防治抗脂阳性和克丁-阴性有机体.盐的盐形式确保稳定性和溶性,促进配方.关键优势包括:与单方丙烯相比,血浆浓度更高,剂量频率降低,胃肠刺激最小化.其浸泡结构允许有效跨越生物膜,使其特别有助于治疗呼吸道,尿道和软组织感染.它适合于临床和研究应用,它保持了丙烯醇的功效,优化了药用.

结构式图片

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CAS号40966-78-7 2-(R)-2-phenyl-... | CAS号69-53-4 氨苄西林

合成工艺路线路线简述

    📜Magnesium Sulfate,氨苄西林,1-溴乙基乙基碳酸酯置于盐酸,碳酸氢钠体系中,用 乙酸丁酯,水,乙酸乙酯,丙酮 作为反应溶剂,化学反应生成 盐酸巴氨西林
    参考文献:Preparation Of 1'-Ethoxycarbonyl-Oxyethyl Esters Of Penicillins
    标题:Preparation Of 1'-Ethoxycarbonyl-Oxyethyl Esters Of Penicillins
    摘要:制备青霉素1'-乙氧羰氧乙酯的过程,其中化合物的结构式为##str1##其中a是苯基,苯氧基或4-羟基苯基,B是氢,氨基或保护的氨基,Z是氢或从碱金属,三(较低烷基)氨基和四(较低烷基)氨基组中选择的阳离子,与1-溴乙基乙基碳酸酯在有机溶剂中反应,当b是保护的氨基时,保护基被去除以产生一次氨基.还提供了结构式为##str2##其中ph是苯基,R是ch.Sub.3--或c.Sub.2H.Sub.5--的新化合物.

    海关参考信息

    专利信息


    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-2007203079-A1
    优先权日:2005-11-21
    标题:Methods of using small molecule compounds for neuroprotection
    发明人:CALDWELL GUY A; CALDWELL KIM A; CAO SONGSONG
    权利人:CALDWELL GUY A; CALDWELL KIM A; CAO SONGSONG
    摘要:Methods are provided for preventing neurodegeneration and neuronal loss by administering compositions comprising small molecule compounds with the effect of preventing neurodegeneration and neuronal loss. In one aspect of the invention, the methods and compositions are also useful for treating neurodegenerative diseases. Small molecule compounds provide an important treatment option because of their stability, ease of use in both manufacture and formulation, ease of administration, and patient compliance. The small molecule compound compositions of the present invention may include topoisomerase II inhibitors, bacterial transpeptidase inhibitors, calcium channel antagonists, cyclooxygenase inhibitors, folic acid synthesis inhibitors, or sodium channel blockers and functional analogues thereof that have an effect on neurodegeneration. The compositions of the present invention may be administered prophylactically before the onset of clinical symptoms or after clinical symptoms of a neurodegenerative disease have manifested.

    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.

    专利号:US-9493497-B2
    优先权日:2012-04-26
    标题:Carbamate glycolipid and use thereof
    发明人:TASHIRO TAKUYA; MORI KENJI; SHIOZAKI MASAO; TANIGUCHI MASARU; WATARAI HIROSHI
    权利人:RIKEN
    摘要:The invention provides a compound effective as an antitumor active agent or vaccine adjuvant and an intermediate useful for the synthesis of the compound, as well as production methods thereof, and a medicament containing the novel compound. The compound is a carbamate glycolipid represented by the formula (I) n nwherein each symbol is as defined herein. The invention also provides a dendritic cell pulsed with the glycolipid.

    专利号:US-9907753-B2
    优先权日:2010-03-19
    标 题 :Lipid vesicle compositions and methods of use
    发明人:IRVINE DARRELL J; MOON JAEHYUN
    权利人:MASSACHUSETTS INST TECHNOLOGY
    摘要:The invention provides delivery systems comprised of stabilized multilamellar vesicles, as well as compositions, methods of synthesis, and methods of use thereof. The stabilized multilamellar vesicles may comprise prophylactic, therapeutic and/or diagnostic agents.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Buonomo A, Nucera E, De Pasquale T, Pecora V, Lombardo C, Sabato V, Colagiovanni A, Rizzi A, Aruanno A, Pascolini L, Patriarca G, Schiavino D. Tolerability of aztreonam in patients with cell-mediated allergy to β-lactams. Int Arch Allergy Immunol. 2011;155(2):155-9. doi: 10.1159/000318844. Epub 2010 Dec 22. English, Italian. French. Japanese. Review. Erratum in: Mayo Clin Proc 1999 Nov;74(11):1184.

    合成参考文献


    参考文献:10.1038/ncb3255
    摘要:Lin R, Elf S, Shan C, Kang HB, Ji Q, Zhou L, Hitosugi T, Zhang L, Zhang S, Seo JH, Xie J, Tucker M, Gu TL, Sudderth J, Jiang L, Mitsche M, DeBerardinis RJ, Wu S, Li Y, Mao H, Chen PR, Wang D, Chen GZ, Hurwitz SJ, Lonial S, Arellano ML, Khoury HJ, Khuri FR, Lee BH, Lei Q, Brat DJ, Ye K, Boggon TJ, He C, Kang S, Fan J, Chen J. 6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling. Nat Cell Biol. 2015 Nov;17(11):1484–96.
    摘要:
    摘要:Chemotherapy, 27(Suppl
    摘要:Gekkan Yakuji. Pharmaceuticals Monthly., 23(1735), 1981
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