首页> 外文学位 >Design and synthesis of foscarnet-peptide conjugates, halogenated bisphosphonates and phosphonocarboxylates and biochemical sensing using film-bulk-acoustic-resonators.
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Design and synthesis of foscarnet-peptide conjugates, halogenated bisphosphonates and phosphonocarboxylates and biochemical sensing using film-bulk-acoustic-resonators.

机译:膦甲酸-肽共轭物,卤代双膦酸酯和膦酰基羧酸酯的设计与合成,以及使用薄膜-体-声-谐振器的生化传感。

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摘要

A practical method for synthesis and isolation of previously elusive deprotected P-N linked foscarnet-amino acid conjugates was developed. The conjugates are good candidates for evaluation as foscarnet prodrugs as they release the active drug quantitatively under physiological conditions leaving only benign amino acids as by-products.; A number of alkyl ester-protected thiophosphonoformate-peptide conjugates were synthesized via coupling between dimethyl-TPFACl and C-alkyl protected amino acids. An easily scalable, safe and cleaner method for synthesis of dimethyl-TPFACl was developed. The conjugates were treated with a series of dealkylating agents, such as t-BuNH2, NaOH, NaI, LiBr etc to produce monoanionic salts. Unfortunately, none of them led to the clean product due to competitive P-C and P-N bond cleavage.; A safe and convenient method for fluorination of phosphonoacetate derivatives was achieved using SelectfluorRTM as fluorine source. Using this reagent either mono- or difluoro analogs were obtained selectively by simple adjustment of base and SelectfluorRTM equivalents in the reaction mixture. The same reagent was used to prepare fluorinated analogs of nitrogen-containing bisphosphonates and phosphonoacarboxylates. Their corresponding chloro- and brominated analogs were also synthesized using N-chlorosuccinamide and N-bromosuccinamide, respectively, as Cl+ and Br+ sources.; For the first time, it was demonstrated that an FBAR device could be used for realtime observation of bio-molecular interactions, such as of biotin-streptavidin, on solid supports without use of labels. Sequence-specific DNA sensing was demonstrated by immobilizing probe DNA on the FBAR surface and measuring the resonance shift in real-time during hybridization with complementary strand. 15-Mer oligonucleotides differing by only one nucleobase could be distinguished. A highly sensitive thin gold film coated FBAR was developed, which was able to detect mercuric ion selectively in water as low as 0.2 ppb, below the maximum allowable concentration in drinking water in the US.
机译:开发了一种实用的合成和分离先前难以捉摸的去保护的P-N连接的膦甲酸酯-氨基酸缀合物的方法。该缀合物是评估膦甲酸酯前药的良好候选物,因为它们在生理条件下定量释放活性药物,仅留下良性氨基酸作为副产物。通过二甲基-TPFAC1和C-烷基保护的氨基酸之间的偶联,合成了许多烷基酯保护的硫代膦酸酯-肽共轭物。开发了一种易于扩展,安全和清洁的二甲基-TPFACl合成方法。用一系列脱烷基剂,例如t-BuNH 2,NaOH,NaI,LiBr等处理缀合物以产生单阴离子盐。不幸的是,由于竞争性的P-C和P-N键断裂,它们都不导致获得清洁产品。使用SelectfluorRTM作为氟源,可以安全,方便地氟化膦酰基乙酸酯衍生物。使用该试剂,可通过简单调节反应混合物中的碱和SelectfluorRTM当量选择性地获得单氟或二氟类似物。使用相同的试剂制备含氮的双膦酸酯和膦酰基羧酸酯的氟化类似物。还分别使用N-氯琥珀酰胺和N-溴琥珀酰胺作为Cl +和Br +源合成了它们相应的氯代和溴代类似物。首次证明,FBAR设备可用于实时观察固体支持物上的生物分子相互作用,例如生物素-链霉亲和素,而无需使用标签。通过将探针DNA固定在FBAR表面并在与互补链杂交的过程中实时测量共振位移,证明了序列特异性DNA的检测。可以区别仅一个核碱基的15-Mer寡核苷酸。开发了一种高灵敏度的金膜薄膜涂覆的FBAR,它能够选择性地检测到低至0.2 ppb的水中的汞离子,低于美国饮用水中的最大允许浓度。

著录项

  • 作者

    Marma, Mong Sano.;

  • 作者单位

    University of Southern California.;

  • 授予单位 University of Southern California.;
  • 学科 Chemistry Biochemistry.; Chemistry Organic.; Chemistry Pharmaceutical.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 240 p.
  • 总页数 240
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;有机化学;药物化学;
  • 关键词

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