CAS: 68892-41-1; N2-Isobutyryl-5'-O-(4,4'-Dimethoxytrityl)-2'-Deoxyguanosine

该化合物是一种合成核素派衍生物,由于有经过改装的guanosine脊椎,具有独特的结构特征.该化合物具有5欧元-欧替代成分,包括双(4-甲基)苯基甲基苯基,这增加了其亲脂性,并有可能加强其生物活动.2欧元-脱氧结构表明,它缺乏位于2欧元位置的氢氧基组,该组具有DNA核素的典型特征,从而影响其稳定性以及与核酸的相互作用.N-(2-甲基-1-氧基丙基)在guanine基上的修改可能会影响其与核糖酸目标的结合性和特殊性.

结构式图片

相似化合物

114745-26-5 81246-83-5 144089-96-3

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

CAS号68892-42-2 N2-异丁酰-2'-脱氧鸟甙 | CAS号40615-36-9 4,4'-二甲氧基三苯基氯甲烷 | CAS号961-07-9 2'-脱氧鸟苷 | CAS号82921-42-4 2'-deoxy-N2-iso... | CAS号132471-94-4 N2-isobutyryl-2... | CAS号64350-24-9 N2-异丁酰基鸟苷一水合物 | CAS号87865-78-9 3',5'-TIPS-N-IBU-鸟苷 | CAS号118-00-3 鸟苷 | CAS号74405-46-2 IBU-DMT-DEOXYGU... | CAS号68892-42-2 N2-异丁酰-2'-脱氧鸟甙 | CAS号81144-43-6 5'-O-(4,4'-二甲氧基... | CAS号84416-84-2 5'-O-(4,4'-DIME... | CAS号63660-23-1 N2-异丁酰基-3'-O-苯甲...

合成工艺路线路线简述

    在 4-二甲氨基吡啶,Ammonium Hydroxide,Tea,1,8-二氮杂双环[5.4.0]十一碳-7-烯体系中,用 吡啶 作为反应溶剂,化学反应 6.0H,反应生成 N2-异丁酰-5'-O-(4,4'-二甲氧基三苯基)-2'-脱氧鸟苷
    参考文献:Awasthi,S. K.; Khanna,V.; Watal,G.,Indian Journal Of Chemistry-Section B Organic And Medicinal Chemistry,1993,Vol. 32,# 9,P. 916-919
    标题:Awasthi,S. K.; Khanna,V.; Watal,G.,Indian Journal Of Chemistry-Section B Organic And Medicinal Chemistry,1993,Vol. 32,# 9,P. 916-919

    专利信息


    专利号:US-2023212204-A1
    优先权日:2020-01-16
    标题:Reagents and their use for modular enantiodivergent synthesis of c-p bonds
    发明人:XU DONGMIN; RIVAS-BASCÓN NAZARET; KNOUSE KYLE W; PADIAL NATALIA; ZHENG BIN; VANTOUROUT JULIEN; SCHMIDT MICHAEL; EASTGATE MARTIN D; BARAN PHI
    权利人:BRISTOL MYERS SQUIBB CO; SCRIPPS RESEARCH INST
    摘要:The disclosure describes chiral P(V)-based reagents and their uses for the modular, scalable, and stereospecific synthesis of chiral phosphines, phosphine oxides and particular oligonucleotides.

    专利号:US-4849513-A
    优先权日:1983-12-20
    标 题 :Deoxyribonucleoside phosphoramidites in which an aliphatic amino group is attached to the sugar ring and their use for the preparation of oligonucleotides containing aliphatic amino groups
    发明人:SMITH LLOYD M; FUNG STEVEN; KAISER ROBERT J
    权利人:CALIFORNIA INST OF TECHN
    摘要:The invention consists of compounds and methods for the synthesis of oligonucleotides which contain one or more free aliphatic amino groups attached to the sugar moieties of the nucleoside subunits. The synthetic method is versatile and general, permitting amino groups to be selectively placed at any position on oligonucleotides of any composition or length which is attainable by current DNA synthetic methods. Fluorescent dyes or other detectable moieties may be covalently attached to the amino groups to yield the corresponding modified oligonucleotide.

    专利号:US-12337291-B2
    优先权日:2017-09-11
    标 题 :Guide RNA synthesis system and method
    发明人:DABROWSKI PAUL; GERLINGHAUS FABIAN; KELSO REED; WALKER II JOHN ANDREW
    权利人:SYNTHEGO CORP
    摘要:The present invention provides improved automated systems and methods for synthesis of biopolymers including DNA and RNA. The automated systems and methods represent a number of improvements over existing systems for multiplex synthesis of biopolymers in a combinatorial fashion.

    专利号:US-2013303745-A1
    优先权日:2007-05-22
    标 题:Synthesis of oligonucleotides
    发明人:LANGE MEINOLF; HOHLFELD ANDREAS; SCHONBERGER ANDREAS; KIRCHHOFF CHRISTINA; GROSSEL OLAF
    权利人:LANGE MEINOLF; HOHLFELD ANDREAS; SCHONBERGER ANDREAS; KIRCHHOFF CHRISTINA; GROSSEL OLAF
    摘要:A method for preparing an oligonucleotide comprising the steps of synthesizing a phosphoramidite by reacting a hydroxyl-containing compound of formula (A) with a phosphitylating agent in the presence of an activator compound of formula (I), to prepare a phosphitylated compound, then coupling the phosphitylated compound without isolation with a second compound having the formula (A), wherein R 5 , R 3 , R 2 , B are independently selected, but have the same definition as above in the presence of an activator II selected from the group of imidazole, imidazolium salts, and mixtures thereof, which are improved activators over activators disclosed in related art.

    专利号:US-5118800-A
    优先权日:1983-12-20
    标 题 :Oligonucleotides possessing a primary amino group in the terminal nucleotide
    发明人:SMITH LLOYD M; FUNG STEVEN; KAISER JR ROBERT J
    权利人:CALIFORNIA INST OF TECHN
    摘要:The invention consists of compounds and methods for the synthesis of oligonucleotides which contain one or more free aliphatic amino groups attached to the sugar moieties of the nucleoside subunits. The synthetic method is versatile and general, permitting amino groups to be selectively placed at any position on oligonucleotides of any composition or length which is attainable by current DNA synthetic methods. Fluorescent dyes or other detectable moieties may be covalently attached to the amino groups to yield the corresponding modified oligonucleotide.

    专利号:US-5015733-A
    优先权日:1983-12-20
    标题 :Nucleosides possessing blocked aliphatic amino groups
    发明人:SMITH LLOYD M; FUND STEVEN; KAISER JR ROBERT J
    权利人:CALIFORNIA INST OF TECHN
    摘要:The invention consists of compounds and methods for the synthesis of oligonucleotides which contain one or more free aliphatic amino groups attached to the sugar moieties of the nucleoside subunits. The synthetic method is versatile and general, permitting amino groups to be selectively placed at any position on oligonucleotides of any composition or length which is attainable by current DNA synthetic methods. Fluorescent dyes or other detectable moieites may be covalently attached to the amino groups to yield the corresponding modified oligonucleotide.
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    主要参考文献

    [参考文献]: Meinolf Lange, Et Al. Synthesis Of Oligonucleotides. Wo2008141682A1.

    合成参考文献


    摘要:McKenna, C. E.; Kashemirov, B. A.; Błażewska, K. M., Science of Synthesis, (2009) 42, 891.
    摘要:McKenna, C. E.; Kashemirov, B. A.; Błażewska, K. M., Science of Synthesis, (2009) 42, 788.
    摘要:McKenna, C. E.; Kashemirov, B. A.; Błażewska, K. M., Science of Synthesis, (2009) 42, 888.
    摘要:McKenna, C. E.; Kashemirov, B. A.; Błażewska, K. M., Science of Synthesis, (2009) 42, 893.
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