Stereoselective Synthesis and Chemical Investigation of Modified DNA Oligomer
Stereoselective Synthesis and Chemical Investigation of Modified DNA Oligomer
批准号:
01571150
负责人:
TANAKA Kiyoshi
金额:
$1.28万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1989
资助国家:
日本
项目状态:
已结题
起止时间:
1989 至 1990
中文摘要
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英文摘要
Chemical investigation on stereoselective synthesis and properties of modified DNA oligomers has been done in order to obtain the information about the elucidation of DNA function systems and development of new type of medicines. During this study, the apparatus such as spinning concentrator, and electrophoretic equipments were efficiently employed for isolation and characterization of the modified DNA molecules. The results of our investigation are summaried as follows :1. Hybridization of functional heterocyclic compounds, flavin, 5-deazaflavin, viologen, with DNA oligomer was effectively achieved in covalent phosphoramidate, using alkylamine as a linker. On the basis of this approach, several modified DNA oligomers have been synthesized, in which the functional hoterocyclic compounds were introduced at the desired site of the sequence.2. After characterization, the stability of the duplex with their comlementary strands was examined. Subsequently, function and capabilities (intercal … More ator, fluorescence-marker, redox and local cleavage reactor) were investigated by means of UV, fluorescence, ESR spectra and HPLC analyses.3. The resistant reactivity of the above strand toward the conventional nuclease was observed at the modified site of the sequence.4. Some kinds of sulfur modified thymidine nucleotides were synthesized, which were incorporated into the desired site of the DNA sequence. The stability of the duplex was investigated by UV and CD spectra, and it turned out that both position of the sulfur and number of the modified base significantly influencedupon the stability and conformation of the duplex.5. Several attempts were made to achieve stereoselective internucleotide bond formation based on phosphoramidite approach under the controlled condition and with chiral auxiliaries. In spite of the effort, no satisfactory results were obtained and this subject remained as a future problem.6. The reductive repair of oxidatively damaged nucleosides was investigated and a proposal that glutathione and reduced coenzyme models might play an important role in the living systems, was made. Less
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Kiyoshi Tanaka: "The Synthesis and Properties of ViologenーOligonucleotide Conjugate Molecules" Bioorg.& Med.Chem.Lett.,. 1. (1991)
Kiyoshi Tanaka:“紫罗碱-寡核苷酸缀合物分子的合成和特性”Bioorg.& Med.Chem.Lett.,1. (1991)
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Kiyoshi Tanaka: "A Novel One-electron Reduction System Consisting of 1,5-Dihydro-5-deazaflavin and Flavinium.Application to the Reductive Repair of 1,3-Dimethylthymine-Bromohydrin as a Model of a Damaged Nucleic Acid" J.Chem.Soc.,Chem.Commun.910-911 (1989
Kiyoshi Tanaka:“一种由 1,5-二氢-5-脱氮黄素和黄素组成的新型单电子还原系统。作为受损核酸模型在 1,3-二甲基胸腺嘧啶-溴醇还原修复中的应用”J.Chem
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Kiyoshi Tanaka: "A Novel Oneーelectron Reduction System Consisting of 1,5ーDihydroー5ーdeazaflavin and Flavinium.Application to the Reductive Repair of 1,3ーDimethylthymineーBromohydrin as a Model of a Damaged Nucleic Acid" J.Chem.Soc.,Chem.Commun.910-911 (1989
Kiyoshi Tanaka:“一种由1,5-二氢-5-去氮黄素和黄素组成的新型单电子还原系统。作为受损核酸模型在1,3-二甲基胸腺嘧啶-溴醇还原修复中的应用” J.Chem .Soc.,Chem.Commun.910-911 (1989
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Kiyoshi Tanaka: "A Novel Oneーelectron Redection System Consisting of 1,5ーDihydroー5ーdeazaflavin and Flavinium.Application to the Redective Repair of 1,3ーDimethylthymineーBromohydrin as a Model of a Damaged Nucleic Acid" J.Chem.Soc.,Chem.Commun.910-911 (1989
Kiyoshi Tanaka:“一种由1,5-二氢-5-去氮黄素和黄素组成的新型单电子还原系统。作为受损核酸模型在1,3-二甲基胸腺嘧啶-溴醇还原修复中的应用” J.Chem .Soc.,Chem.Commun.910-911 (1989
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Kiyoshi Tanaka et al.: "A Novel One-electron Reduction System Consisting of 1, 5-Dihydro-5-deazaflavin and flavinium. Application to the Reductive Repair of 1, 3-Dimethylthmine- Bromohydrin as a Model of a Damaged Nucleic Acid" J. Chem. Soc., Chem. Commun
Kiyoshi Tanaka 等人:“一种由 1, 5-二氢-5-去氮黄素和黄素组成的新型单电子还原系统。作为受损核酸模型在 1, 3-二甲三胺-溴醇还原修复中的应用”
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New Development of Asymmetric Olefination
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海外基金