CAS: 2180-92-9; 1-Butyl-N-(2,6-Dimethylphenyl)Piperidine-2-Carboxamide

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1-bromo-butane bupivacaine hydr°Chloride (+)-Bupivacaine racemic 1-butylpiperidine-2-carboxylic acid(+)-Bupivacaine levobupivacaine

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    专利号:US-2012177593-A1
    优先权日:2009-07-20
    标 题 :Synthesis of dendrimer conjugates
    发明人:BAKER JR JAMES R; ZHANG YUEHUA; THOMAS THOMMEY P; DESAI ANKUR MAHESH
    权利人:BAKER JR JAMES R; ZHANG YUEHUA; THOMAS THOMMEY P; DESAI ANKUR MAHESH; UNIV MICHIGAN
    摘要:The present invention relates to novel methods of synthesis of therapeutic and diagnostic dendrimers. In particular, the present invention is directed to novel dendrimer conjugates, novel methods of synthesizing the same, compositions comprising the conjugates, as well as systems and methods utilizing the conjugates (e.g., in diagnostic and/or therapeutic settings (e.g., for the delivery of therapeutics, imaging, and/or targeting agents (e.g., in disease (e.g., cancer, inflammatory disease) diagnosis and/or therapy, pain therapy, etc.)). Accordingly, dendrimer conjugates of the present invention may further comprise at least two different components for targeting, imaging, sensing, and/or providing a therapeutic or diagnostic material and/or monitoring response to therapy. Furthermore, the novel synthesis methods of certain embodiments of the present invention provide significant advantages with regard to total reaction time and simplicity.

    专利号:US-2014205671-A1
    优先权日:2013-01-18
    标题 :Synthesis and use of polyhydroxyalkanoate (pha) nanocapsules as a protein carrier
    发明人:YU PETER HOI FU; CHAN ALEX HO YIN; HO KWOK PING
    权利人:NANO & ADVANCED MATERIALS INST LTD
    摘要:A method of synthesizing PHA nanocapsules as a protein carrier, particularly, the synthesis of PHA nanocapsules synthesized by a modified precipitation/solvent evaporation technique with neutralization. Specifically, the method comprises the steps of sonicating a first solution comprising a triblock PHA copolymer, stirring the first solution into a second solution to give a third solution, the second solution containing a protein, and the second solution being acidic. Further, the method comprises adding the third solution with a neutralizing agent to give a neutralized solution, and sonicating the neutralized solution to form a final solution, wherein the synthesized PHA nanocapsules containing the protein are formed in the final solution. Further, PHA nanocapsules encapsulated with the protein is used by administering the synthesized PHA nanocapsule to an animal in need thereof via the oral cavity.

    专利号:US-2023047214-A1
    优先权日:2020-02-03
    标题:Methods for microwave synthesis of degradable polymers for drug delivery
    发明人:MURATOGLU ORHUN K; ORAL EBRU; GRINDY SCOTT
    权利人:MASSACHUSETTS GEN HOSPITAL
    摘要:Provided herein are methods of making degradable, additive-blended polymeric materials using microwave radiation and catalysts. The methods can include incorporation of therapeutic materials into the polymeric materials. There also are provided polymeric materials made by the methods and medical devices comprising the polymeric materials made by the methods.

    专利号:US-12295961-B2
    优先权日:2009-12-31
    标 题:Modulation of solubility, stability, absorption, metabolism, and pharmacokinetic profile of lipophilic drugs by sterols
    发明人:DHINGRA OM
    权利人:MARIUS PHARMACEUTICALS INC
    摘要:A formulation for drug delivery, providing enhanced modulation of solubility, stability, absorption, metabolism, and/or pharmacokinetic profile of a lipophilic therapeutic agent by formulation with sterols and/or sterol esters, resulting in higher bioavailability of a therapeutic agent administered to a subject in need of such therapeutic agent. The formulation contains a therapeutic agent and a sterol or sterol ester, and can, optionally, further contain a solubilizer and/or an enhancing agent. Also described are pharmaceutical compositions containing the formulations and methods of making and methods of using the formulations and pharmaceutical compositions. Formulations of the disclosure can be constituted to minimize the synthesis of dihydrotestosterone when the therapeutic agent includes testosterone or testosterone esters.

    专利号:WO-9964032-A1
    优先权日:1998-06-08
    标题 :Combinatorial synthesis of multibinding libraries
    发明人:CHRISTENSEN BURTON G; GRIFFIN JOHN H; JENKINS THOMAS E; JUDICE J KEVIN
    权利人:ADVANCED MEDICINE INC; CHRISTENSEN BURTON G; GRIFFIN JOHN H; JENKINS THOMAS E; JUDICE J KEVIN
    摘要:Disclosed are methods for synthesizing large collections of diverse multimeric compounds as well as iterative processes for evaluating key molecular constraints imparting multibinding properties to multimeric compounds. Also disclosed are libraries of multimeric compounds which can be evaluated for imparting multibinding properties.

    专利号:WO-9628426-A1
    优先权日:1995-03-10
    标 题 :N-alkylpipecolic acid compounds, their preparation and use in the synthesis of levobupivacaine and analogues
    发明人:DYER ULRICH CONRAD; ZAVAREH HOOSHANG SHAHRIARI
    权利人:CHIROSCIENCE LTD; DYER ULRICH CONRAD; ZAVAREH HOOSHANG SHAHRIARI
    摘要:Optically-enriched N,O-dialkyl pipecolates are useful in the preparation of levobupivacaine and related analgesics. They may be prepared simply by dialkylating optically-enriched pipecolic acid by reaction with an alkylating agent, in the presence of base and a polar aprotic solvent.
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    参考文献:10.1007/s00101-009-1673-2
    摘要:Wallenborn J; German Society for Anesthesiology and Intensive Care Medicine; Professional Association of German Anesthetists; German Society for Gynecology and Obstetrics. [Execution of analgesia and anesthesia procedures in obstetrics : Second revised recommendations of the German Society for Anesthesiology and Intensive Care Medicine and the Professional Association of German Anesthetists in cooperation with the German Society for Gynecology and Obstetrics]. Anaesthesist. 2010 Mar;59(3):250–4. doi: 10.1007/s00101-009-1673-2.
    参考文献:10.1016/j.neuroscience.2010.02.015
    摘要:Pereira M, Morrell JI. The medial preoptic area is necessary for motivated choice of pup- over cocaine-associated environments by early postpartum rats. Neuroscience. 2010 May;167(2):216–31. doi: 10.1016/j.neuroscience.2010.02.015.
    参考文献:10.1007/s00264-010-0968-x
    摘要:Wang J, Huang T, Ma H, Hung S, Chen T, Liu C. Manipulation under anaesthesia for frozen shoulder in patients with and without non-insulin dependent diabetes mellitus. International Orthopaedics (SICOT). 2010 Feb 17;34(8):1227–32. doi: 10.1007/s00264-010-0968-x.
    参考文献:10.1007/s00540-010-0884-7
    摘要:Zanette G, Micaglio M, Zanette L, Manani G, Facco E. Comparison between ketamine and fentanyl–droperidol for rectal premedication in children: a randomized placebo controlled trial. Journal of Anesthesia. 2010 Feb 17;24(2):197–203. doi: 10.1007/s00540-010-0884-7.
    参考文献:10.1111/j.1460-9592.2010.03259.x
    摘要:Akin A, Ocalan S, Esmaoglu A, Boyaci A. The effects of caudal or intravenous clonidine on postoperative analgesia produced by caudal levobupivacaine in children. Paediatr Anaesth. 2010 Apr;20(4):350–5. doi: 10.1111/j.1460-9592.2010.03259.x.
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