CAS: 77-39-4; Cycrimine

该化合物是它能够抑制对肌肉受体的乙酰胆碱酯酶作用,这可能导致分泌减少,肌肉松动和心率提高等效应.Cycrimine经常用于治疗各种病症,包括运动疾病和某些肠胃紊乱.该化合物一般是白到白的晶状固体,在有机溶剂中可溶解.其药理学特征包括相对快速的行动开始,使其对急性症状有效.然而,与许多抗胆碱菊酯酶一样,它也可能产生副作用,如口干口,视力模糊和尿液保留,因为它对胆碱系统具有系统性影响.安全和功效是最重要的,应当监测其使用情况,特别是在敏感到抗胆碱效应的人群中.

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CAS号73-63-2 Β-哌啶子基苯丙酮 | CAS号33240-34-5 环戊基溴化镁

合成工艺路线路线简述

    📜3-(1-哌啶基)苯丙酮盐酸盐,环戊基溴化镁置于乙醚体系中,化学反应生成 赛克立明
    参考文献:Antispasmodics. Vi.1 Additional Substituted Beta Amino Ketones
    标题:Antispasmodics. Vi.1 Additional Substituted Beta Amino Ketones
    摘要:
    DOI:10.1021/ja01164A126

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    专利信息


    专利号:US-2023271983-A1
    优先权日:2020-07-29
    标题 :Functionalized isonitriles and products, preparation and uses thereof
    发明人:SOTELO PÉREZ EDDY; AZUAJE GUERRERO JHONNY ALBERTO; MAJELLARO MARIA
    权利人:UNIV SANTIAGO COMPOSTELA
    摘要:The present invention relates to functionalized isonitrile compounds, formed by means of multicomponent environmentally friendly reactions, suitable for coupling to functional molecules such as biomolecules, APIs, chromophore and fluorophore molecules. The invention also relates to conjugates between said isonitrile compounds and functional molecules, which are useful in the synthesis of pharmaceutic drugs or tools, fluorescent molecules and labels, polymeric smart materials. The invention furthermore provides a kit for the in-vitro preparation of the functionalized isontrile compounds and conjugates. The invention also contemplates the medical use of said compounds and conjugates.

    专利号:US-2005053642-A1
    优先权日:2000-08-23
    标题:Biocompatible materials
    发明人:ULBRICHT MATHIAS; THOM VOLKMAR; JANKOVA KATJA; ALTANKOV GEORGE; JONSSON GUNNAR
    摘要:The present invention teaches a novel approach of creating biocmpatible surfaces, said surfaces being capable of functionally interact with biological material. SAid biocompatible surfaces comrise at least two comonents, such as a hydrophobic substratum and a macromolecule of hydrophilic nature, which, in a cooperativity, form together the novel biocoompatible surfaces. The novel approach is ased on contacting said hydrophobic substratum with a laterally patterned monomolecular layer of said hydrophilic and flexible macromolecules, exhibiting a pronounced excluded volume. The htus formed two component surface is, in respect to polarity and morphology, a molecularly heterogeneous surface. Structural features of said macromolecular monolayer (as e.g. the layer thickness or its lateral density) are determined by: i) the structural features of the layer forming macromolecules (as e.g. their MW or their molecular architecture) and ii) the method of creating said monomolecular layer (as e.g. by physi- or chemisorbing, or by chemically binding said macromolecules). The structural features of the layer forming macromolecules(s) is in turn determined by synthesis. AMount and conformation and thus also biological activity of biological material (as e.g. polypeptides) which contact the novel biocompatible surface, is determined and maintained by the cooperative action of the underlying hydrophobic substratum and the macromolecular layer. In this way it becomes possible to maintain and control biological interactions between said contacted polypeptides and other biological compounds as e.g. cells, antibodies and the like. Consequently, the present invention aims to reduce and/or eliminate the deactivation and/or denaturation associated with the contacting of polypeptides and/or other biological material to a hydrophobic substratum surface.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Winger RH, Liedl KR, Sotriffer CA, Gamper AM, Rode BM, Kroemer RT, Varga JM. Prediction of IgE(Lb4)-ligand complex structures by automated docking. J Mol Recognit. 1996 May-Jun;9(3):239-46. Italian. Spanish. French.

    合成参考文献


    参考文献:10.1007/bf00124500
    摘要:Sotriffer CA, Winger RH, Liedl KR, Rode BM, Varga JM. Comparative docking studies on ligand binding to the multispecific antibodies IgE-La2 and IgE-Lb4. Journal of Computer-Aided Molecular Design. 1996 Aug;10(4):305–20. doi: 10.1007/bf00124500.
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