CAS: 2312-73-4; N-Benzyl-9-(Tetrahydro-2H-Pyran-2-yl)-9H-Purin-6-Amine

该化合物是一种纯衍生物,其结构复杂,包括一个与一个苯甲基组相连的纯基和四氢-2H-pyran moth,该化合物通常具有与纯相关的特性,例如潜在的生物活动,包括与核糖酸结构和酶的相互作用;其分子结构表明,由于有矿和氢氧组的存在,它可能参与氢联结,影响其溶解性和再活性;四氢-平环有助于其立体化学特性,并可能影响其药用植物特性;这种性质的化合物由于它们具有模拟天然核糖基的能力,因此经常被研究其潜在的治疗用途,特别是在医药化学和药物设计领域.然而,熔点,溶液和生物活动等具体特性需要实证数据才能精确评估.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号7306-68-5 6-氯-9-(四氢-2-吡喃基)嘌呤 | CAS号100-46-9 苄胺 | CAS号110-87-2 3,4-二氢-2H-吡喃 | CAS号1214-39-7 6-苄氨基嘌呤 | CAS号19769-32-5 6-methylsulfony... | CAS号50-66-8 6-甲巯基嘌呤

合成工艺路线路线简述

  • 合成目标产物 N-Benzyl-9-(Tetrahydro-2H-Pyran-2-yl)Adenine 主要起始原料 6-Chloro-9-(Tetrahydro-2-Pyranyl)-Purine And Benzylamine
  • (文献来源)合成步骤主要原料 6-Chloro-9-(Tetrahydro-2-Pyranyl)-Purine 和 Benzylamine
📜6-甲巯基嘌呤置于三氯异氰尿酸,对甲苯磺酸体系中,用 甲醇,水,正丁醇 用作溶剂,化学反应 4.25H,反应生成苄吡喃腺嘌呤
参考文献:Villar,Jose Daniel Figueroa; Motta,Marita Almeida,Nucleosides,Nucleotides And Nucleic Acids,2000,Vol. 19,# 5-6,P. 1005-1015
标题:Villar,Jose Daniel Figueroa; Motta,Marita Almeida,Nucleosides,Nucleotides And Nucleic Acids,2000,Vol. 19,# 5-6,P. 1005-1015

海关参考信息

专利信息


专利号:US-6867305-B2
优先权日:1996-12-03
标题:Synthesis of epothilones, intermediates thereto and analogues thereof
发明人:DANISHEFSKY SAMUEL J; STACHEL SHAWN J; LEE CHUL BOM; CHAPPELL MARK D; WU ZHICAL
权利人:SLOAN KETTERING INST CANCER; UNIV COLUMBIA
摘要:The present invention provides convergent processes for preparing epothilones, desoxyepothilones, and analogues thereof. The present invention further provides novel compositions and methods for the treatment of cancer and additionally provides methods for the treatment of cancer which has developed a multi-drug phenotype.

专利号:US-2009117125-A1
优先权日:2007-11-07
标 题:Synthesis of 8h-3a-aza-cyclopenta[a]indenes and 5,10-dihydropyrrolo[1,2-b]isoquinolines derivatives and their use as antitumor therapeutic agents

专利号:EP-4245856-B1
优先权日:2022-03-15
标题 :Synthesis of functional unspecific peroxidases using a non-fungal eukaryotic cell-free system
发明人:WALTER RUBEN; KUBICK STEFAN; ZEMELLA ANNE
权利人:FRAUNHOFER GES FORSCHUNG

专利号:WO-2013155481-A1
优先权日:2012-04-13
标 题:Improved cellodextrin transport and mixed sugar fermentation
发明人:DOUDNA CATE JAMES H; GALAZKA JONATHAN M; JIN YONG-SU; HA SUK-JIN
权利人:UNIV ILLINOIS; UNIV CALIFORNIA
摘要:The present disclosure relates to compositions and methods for increasing the transport of cellodextrin into cells, for increasing growth of cells, for increasing synthesis of hydrocarbons and hydrocarbon derivatives, and for co-fermenting cellulose-derived and hemicellulose-derived sugars.

专利号:EP-4245856-A1
优先权日:2022-03-15
标 题 :Synthesis of functional unspecific peroxidases using a non-fungal eukaryotic cell-free system

专利号:CN-115745857-A
优先权日:2022-10-28
标 题 :Active oxygen-responsive thioester compound, synthesis method and use of a class of oral administration

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Anato M, Ketema T. Anti-plasmodial activities of Combretum molle (Combretaceae) [Zwoo] seed extract in Swiss albino mice. BMC Res Notes. 2018 May 18;11(1):312. doi: 10.1186/s13104-018-3424-4. doi: 10.1016/j.biopha.2018.05.030. [Epub ahead of print] doi: 10.1016/j.jcis.2018.05.017. [Epub ahead of print] doi: 10.1186/s12889-018-5537-z. doi: 10.1039/c8cp01609g. doi: 10.1186/s12967-018-1493-8.
13: Shin DH, Leem DG, Shin JS, Kim JI, Kim KT, Choi SY, Lee MH, Choi JH, Lee KT. Compound K induced apoptosis via endoplasmic reticulum Ca(2+) release through ryanodine receptor in human lung cancer cells. J Ginseng Res. 2018 Apr;42(2):165-174. doi: 10.1016/j.jgr.2017.01.015. Epub 2017 Feb 4.
14: Corinti D, Catone D, Turchini S, Rondino F, Crestoni ME, Fornarini S. Photoionization mass spectrometry of ω-phenylalkylamines: Role of radical cation-π interaction. J Chem Phys. 2018 Apr 28;148(16):164307. doi: 10.1063/1.5027786. doi: 10.1016/j.bios.2018.04.050. Epub 2018 Apr 24. doi: 10.1159/000489367. Epub 2018 Apr 25. doi: 10.1016/j.taap.2018.04.025. [Epub ahead of print]

合成参考文献


参考文献:10.1007/978-1-59745-191-8_17
摘要:Tanaka Y, Nakamura N, Togami J. Altering flower color in transgenic plants by RNAi-mediated engineering of flavonoid biosynthetic pathway. Methods Mol Biol. 2008;442():245–57. doi: 10.1007/978-1-59745-191-8_17.
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