CAS: 539-21-9; Ambazone

该化合物是一种化学化合物,属于被称为Azo染色物的有机化合物类别,其特点是其充满活力的颜色,这是许多染色物和颜料中常见的Azo功能组(N=N-)的结果,安巴zon通常用于各种用途,包括纺织品和墨水,因为其具有发扬强色的能力;该化合物在正常条件下具有稳定性,尽管它可能敏感于光和热,从而影响其色素.此外,与许多Azo化合物一样,安巴松在某些环境条件下可能发生退化,导致潜在有害产品释放.在处理安巴松时,安全考虑十分重要,因为一些亚巴松染料与健康风险有关,包括潜在的致癌影响.因此,在使用和处置过程中应当遵循适当的安全协议.总的来说,安巴松是合成染色的显著例子,并具有具体的应用和安全考虑.

结构式图片

上下游产品

CAS号61566-17-4 dihydroambazone | CAS号7316-92-9 Hydrazinecarbox... | CAS号79-19-6 硫代氨基脲

合成工艺路线路线简述

    二氢安巴腙置于potassium Hexacyanoferrate(Iii)体系中,化学反应 2.0H,以100%的收率获得产物安巴腙
    参考文献:Miosga; Schulze; Hesse,Pharmazie,1988,Vol. 43,# 8,P. 541-543
    标题:Miosga; Schulze; Hesse,Pharmazie,1988,Vol. 43,# 8,P. 541-543

    专利信息


    专利号:US-2007021349-A1
    优先权日:2005-04-28
    标题:Orthogonally protected bifunctional amino acid
    发明人:SRINIVASAN ANANTH; LUYT LEONARD G
    权利人:SRINIVASAN ANANTH; LUYT LEONARD G
    摘要:The present invention concerns novel orthogonally protected amino acids, there production and use for the synthesis of binding compounds usable in the diagnosis and treatment of proliferative diseases, in particular tumor diseases.

    专利号:WO-2006114323-A3
    优先权日:2005-04-28
    标题 :Orthogonally protected bifunctional amino acid
    发明人:SRINIVASAN ANANTH; LUYT LEONARD G
    权利人:SCHERING AG; SRINIVASAN ANANTH; LUYT LEONARD G
    摘要:The present invention concerns novel orthogonally protected amino acids, there production and use for the synthesis of binding Compounds usable in the diagnosis and treatment of proliferative diseases, in particular tumor diseases.

    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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    主要参考文献


    1: Fulga I, Neguţ M, Năşcuţiu AM, Nemet C, Toma F, Grigore L, Niţescu R, Marcu C, Nedelcu L, Spircu T. [Microbial sensitivity to ambazone (Faringosept) in pharyngeal samples from patients with acute infections of the upper respiratory tract]. Bacteriol Virusol Parazitol Epidemiol. 2007 Jan-Jun;52(1-2):19-27. Romanian. Review. German.

    合成参考文献


    参考文献:10.1080/15376510701857262
    摘要:Kruhlak NL, Choi SS, Contrera JF, Weaver JL, Willard JM, Hastings KL, Sancilio LF. Development of a Phospholipidosis Database and Predictive Quantitative Structure-Activity Relationship (QSAR) Models. Toxicology Mechanisms and Methods. 2008 Jan;18(2-3):217–27. doi: 10.1080/15376510701857262.
    摘要:Archives of Toxicology, Supplement., 11(P6), 1987
    摘要:Drugs in Japan, 6(57), 1982
    摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
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