CAS: 29701-07-3; (2R,3S,4R,5R,6R)-5-Amino-2-(Aminomethyl)-6-(((1R,2S,3S,4R,6S)-4,6-Diamino-3-(((2S,3R,4S,5S,6R)-4-Amino-3,5-Dihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2-yl)Oxy)-2-Hydroxycyclohexyl)Oxy)Tetrahydro-2H-Pyran-3,4-Diol Sulfate

该化合物是一个复杂的胶层,具有明显的结构特征,有助于其生物活动;该化合物的特征是其甘醇联系,涉及多种糖糖糖,特别是脱氧糖和氨基糖,表明其在抗生素活动方面的潜在作用;硫酸盐组的存在表明,它可能加强了生物系统中的溶性和再活性;D-苯丙胺主要因其作为某些微化酶抗生酶的组成部分的作用而闻名,这些抗生激素对一系列细菌感染有效;其结构允许与细菌肋骨发生相互作用,抑制蛋白合成,从而产生抗微生物效应;该物质的立体化学学学,特别是凝糖晶体元件的配置,对于其生物功能至关重要.总体而言,D-strepatami的独特结构特征有助于其药理特性及其在医药化学中的重要性.

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    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: Uchiyama T, Molgo J, Lemeignan M. Presynaptic effects of bekanamycin at the frog neuromuscular junction. Reversibility by calcium and aminopyridines. Eur J Pharmacol. 1981 Jul 10;72(4):271-80. doi: 10.1016/0014-2999(81)90564-1. 24(4):339-45. 4(10):998-1007. doi: 10.1002/cbic.200300680. 30(2):288-94. German. 25(3):75-87. doi: 10.1540/jsmr1965.25.75. 1188(2):331-3. doi: 10.1016/j.chroma.2008.01.088. Epub 2008 Mar 4. 10(5):464-70. doi: 10.1002/mus.880100514. 7(1):30-3. doi: 10.1039/b813252f. Epub 2008 Oct 30. 24(1):120. doi: 10.1186/s12864-023-09234-3.
    10: Fosso MY, Shrestha SK, Green KD, Garneau-Tsodikova S. Synthesis and Bioactivities of Kanamycin B-Derived Cationic Amphiphiles. J Med Chem. 2015 Dec 10;58(23):9124-32. doi: 10.1021/acs.jmedchem.5b01375. Epub 2015 Dec 1.
    11: Renna G, Siro-Brigiani G, Cagiano R, Cuomo V. Effects of two new aminoglycoside antibiotics on the rat sciatic nerve-gastrocnemius muscle preparation. Arzneimittelforschung. 1983;33(10):1473-4. 8(6):e00747. doi: 10.1002/mbo3.747. Epub 2018 Nov 17.

    合成参考文献


    摘要:Drugs in Japan, 6(742), 1982
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