13015-87-7 + 85-61-0 = 61-19-8 + 72-89-9 反应条件:1.1C:1H-Imidazole,S:H2O,10 Min,Rt 标题:A Simple And Efficient Method To Prepare Thio-Esters In Aqueous Solutions 作者:By Coleman,Tricia M. Et Al 参考文献:Tetrahedron Letters 日期:2005 卷标:46(25) 页码:4307-4310]
56-65-5 = 61-19-8 + 13050-93-6 + 58-64-0 + 690199-49-6 + 55612-37-8 反应条件:1.1R:Naod,C:1801427-51-9,S:D2O,37°C,Ph 7.4 标题:Intrinsic Apyrase-Like Activity Of Cerium-Based Metal-Organic Frameworks (Mofs): Dephosphorylation Of Adenosine Tri- And Diphosphate 作者:By Yang,Jian Et Al 参考文献:Angewandte Chemie 日期:2020 卷标:59(51) 页码:22952-22956]
344911-72-4 = 61-19-8 + 916981-64-1 + 916981-65-2 + 2596-55-6 反应条件:1.1R:4-Ethylmorpholine,C:Pb(No3)2,S:H2O,1 D,20°C,Ph 7.3 标题:Chiral Selection In Oligoadenylate Formation In The Presence Of A Metal Ion Catalyst Or Poly(U) Template 作者:By Osawa,Kazuomi Et Al 参考文献:Origins Of Life And Evolution Of Biospheres 日期:2005 卷标:35(3) 页码:213-223]
73-24-5 + 50-69-1 = 61-19-8 + 56-65-5 + 58-64-0 反应条件:1.1R:Po43-,R:H2O,2 H,150°C 标题:Confinement And Time Immemorial: Prebiotic Synthesis Of Nucleotides On A Porous Mineral Nanoreactor 作者:By Rodrigues,Francisco Et Al 参考文献:Journal Of Physical Chemistry Letters 日期:2019 卷标:10(15) 页码:4192-4196
β-烟酰胺腺嘌呤二核苷酸置于ammonium Hydroxide,P-G-Grain Nadase,三羟甲基氨基甲烷盐酸盐,Magnesium Chloride体系中,化学反应 30.0H,反应生成 5'-腺嘌呤核苷酸 参考文献:Enzymatic Synthesis Of New Pyridine Nucleosides. Clitidine And Its Amide Derivative 标题:Enzymatic Synthesis Of New Pyridine Nucleosides. Clitidine And Its Amide Derivative 摘要:两种β-Nad类似物是通过猪脑nad酶催化的碱基交换反应制备的.这些类似物被证实含有甲基1,4-二氢-4-亚氮喹啉酸盐和1,4-二氢-4-亚氮喹啉胺基团.通过对这些类似物进行连续的水解降解,获得了具有3-羧基和3-氨基甲酰基的1,4-二氢-4-亚氮吡啶β-核糖苷,产率很好.前一种化合物与最近从毒蘑菇分离出的毒性吡啶核苷克利替定相同.本次合成确认了克利替定的1,4-二氢-4-亚氮β-核糖苷结构.初步生物测试表明,3-氨基甲酰基化合物的毒性高于克利替定,这表明克利替定的酰胺衍生物是在毒蘑菇中的一种重要毒性物质. DOI:10.1246/bcsj.54.212
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合成参考文献
参考文献:10.1073/pnas.2005463117 摘要:Abrams RPM, Yasgar A, Teramoto T, Lee MH, Dorjsuren D, Eastman RT, Malik N, Zakharov AV, Li W, Bachani M, Brimacombe K, Steiner JP, Hall MD, Balasubramanian A, Jadhav A, Padmanabhan R, Simeonov A, Nath A. Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. Proc Natl Acad Sci U S A. 2020 Dec 08;117(49):31365–75.