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2'-deoxy-4'-ethyl-2'-fluorocytidine | 1445379-74-7

中文名称
——
中文别名
——
英文名称
2'-deoxy-4'-ethyl-2'-fluorocytidine
英文别名
4-Amino-1-((2R,3R,4R,5R)-5-ethyl-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one;4-amino-1-[(2R,3R,4R,5R)-5-ethyl-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
2'-deoxy-4'-ethyl-2'-fluorocytidine化学式
CAS
1445379-74-7
化学式
C11H16FN3O4
mdl
——
分子量
273.264
InChiKey
WRHBWEWELIFEKF-PKIKSRDPSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    487.1±55.0 °C(Predicted)
  • 密度:
    1.60±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    108
  • 氢给体数:
    3
  • 氢受体数:
    5

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2'-deoxy-4'-ethyl-2'-fluorocytidine吡啶咪唑2,4,6-三甲基吡啶四丁基氟化铵silver nitrate 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 3.0h, 生成 1-((2R,3R,4R,5R)-5-ethyl-3-fluoro-5-(hydroxymethyl)-4-((4-methoxyphenyl)diphenylmethoxy)tetrahydrofuran-2-yl)-4-(((4-methoxyphenyl)diphenylmethyl)amino)pyrimidin-2(1H)-one
    参考文献:
    名称:
    [EN] SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF
    [FR] NUCLÉOSIDES, NUCLÉOTIDES SUBSTITUÉS ET LEURS ANALOGUES
    摘要:
    本文揭示了核苷、核苷酸及其类似物,包括一个或多个核苷、核苷酸及其类似物的药物组合物,以及它们的合成方法。本文还揭示了利用核苷、核苷酸及其类似物改善和/或治疗疾病和/或病况的方法,包括使用核苷、核苷酸和其类似物治疗诺如病毒感染的方法。
    公开号:
    WO2014209979A1
  • 作为产物:
    描述:
    4-amino-1-((2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-5-ethyl-3-fluorotetrahydrofuran-2-yl)pyrimidin-2(1H)-one 在 氟化铵 作用下, 以 甲醇 为溶剂, 反应 14.0h, 以1.6 g的产率得到2'-deoxy-4'-ethyl-2'-fluorocytidine
    参考文献:
    名称:
    发现用于治疗人类呼吸道合胞病毒的一流​​RSV聚合酶抑制剂4'-氯甲基-2'-脱氧3',5'-二-O-异丁酰基-2'-氟胞苷(ALS-8176)感染
    摘要:
    呼吸道合胞病毒(RSV)是儿童期的主要病原体,与明显的发病率和死亡率有关。迄今为止,利巴韦林是唯一获准使用的小分子药物,用途有限。唯一的其他RSV药物是帕利珠单抗(palivizumab),一种单克隆抗体,可用于RSV预防。显然,迫切需要小分子RSV药物。本文报道了一系列4'-取代胞苷核苷的设计,合成,抗RSV活性,代谢和药代动力学。在测试的化合物中,4'-氯甲基-2'-脱氧-2'-氟胞苷(2c)在RSV复制子测定中表现出最有希望的活性,EC 50为0.15μM。2c(2c - TP的5'-三磷酸)抑制RSV聚合酶的IC 50为0.02μM,而对100μM的人DNA和RNA聚合酶没有明显的抑制作用。ALS-8176(71)是2c的3',5'-二-O-异丁酰基前药,在体内具有良好的口服生物利用度和2c - TP高水平。化合物71是一流的核苷RSV聚合酶抑制剂,在2期临床RSV攻击研究中显示出优异的抗RSV功效和安全性。
    DOI:
    10.1021/jm5017279
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文献信息

  • SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF
    申请人:Alios BioPharma, Inc.
    公开号:US20130165400A1
    公开(公告)日:2013-06-27
    Disclosed herein are nucleosides, nucleotides and analogs thereof, pharmaceutical compositions that include one or more of nucleosides, nucleotides and analogs thereof, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an infection from a paramyxovirus and/or an orthomyxovirus, with a nucleoside, a nucleotide and an analog thereof.
    本文披露了核苷、核苷酸及其类似物,包括一个或多个核苷、核苷酸及其类似物的药物组合物,以及它们的合成方法。本文还披露了使用核苷、核苷酸和其类似物来改善和/或治疗疾病和/或病况的方法,包括使用核苷、核苷酸和其类似物来治疗副粘病毒和/或正粘病毒感染的方法。
  • [EN] SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF<br/>[FR] NUCLÉOSIDES, NUCLÉOTIDES SUBSTITUÉS ET ANALOGUES DE CEUX-CI
    申请人:ALIOS BIOPHARMA INC
    公开号:WO2013142525A1
    公开(公告)日:2013-09-26
    Disclosed herein are nucleosides, nucleotides and analogs thereof, pharmaceutical compositions that include one or more of nucleosides, nucleotides and analogs thereof, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an infection from a paramyxovirus and/or an orthomyxovirus, with a nucleoside, a nucleotide and an analog thereof.
    本文披露了核苷、核苷酸及其类似物,包括一个或多个核苷、核苷酸及其类似物的制药组合物,以及其合成方法。本文还披露了使用核苷、核苷酸和其类似物改善和/或治疗疾病和/或病况的方法,包括从副黏病毒和/或正黏病毒感染中治疗。
  • [EN] SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF<br/>[FR] NUCLÉOSIDES SUBSTITUÉS, NUCLÉOTIDES SUBSTITUÉS ET ANALOGUES DE CEUX-CI
    申请人:ALIOS BIOPHARMA INC
    公开号:WO2013096679A1
    公开(公告)日:2013-06-27
    Disclosed herein are nucleosides, nucleotides and analogs thereof, pharmaceutical compositions that include one or more of nucleosides, nucleotides and analogs thereof, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an infection from a paramyxovirus and/or an orthomyxovirus, with a nucleoside, a nucleotide and an analog thereof.
    本文披露了核苷、核苷酸及其类似物,包括一个或多个核苷、核苷酸及其类似物的制药组合物,以及其合成方法。本文还披露了使用核苷、核苷酸和其类似物来改善和/或治疗疾病和/或病况的方法,包括来自副黏病毒和/或正黏病毒的感染。
  • Substituted nucleosides, nucleotides and analogs thereof
    申请人:Alios BioPharma, Inc.
    公开号:US10464965B2
    公开(公告)日:2019-11-05
    Disclosed herein are nucleosides, nucleotides and analogs thereof, pharmaceutical compositions that include one or more of nucleosides, nucleotides and analogs thereof, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an infection from a paramyxovirus and/or an orthomyxovirus, with a nucleoside, a nucleotide and an analog thereof.
    本文公开了核苷、核苷酸及其类似物,包括一种或多种核苷、核苷酸及其类似物的药物组合物,以及合成这些物质的方法。本文还公开了用核苷、核苷酸及其类似物改善和/或治疗疾病和/或病症的方法,包括副粘病毒和/或正粘病毒感染。
  • Discovery of β-d-2′-deoxy-2′-α-fluoro-4′-α-cyano-5-aza-7,9-dideaza adenosine as a potent nucleoside inhibitor of respiratory syncytial virus with excellent selectivity over mitochondrial RNA and DNA polymerases
    作者:Michael O. Clarke、Richard Mackman、Daniel Byun、Hon Hui、Ona Barauskas、Gabriel Birkus、Byoung-Kwon Chun、Edward Doerffler、Joy Feng、Kapil Karki、Gary Lee、Michel Perron、Dustin Siegel、Swami Swaminathan、William Lee
    DOI:10.1016/j.bmcl.2015.04.073
    日期:2015.6
    Novel 4'-substituted beta-D-2'-deoxy-2'-alpha-fluoro (2'd2'F) nucleoside inhibitors of respiratory syncytial virus (RSV) are reported. The introduction of 4'-substitution onto 2'd2'F nucleoside analogs resulted in compounds demonstrating potent cell based RSV inhibition, improved inhibition of the RSV polymerase by the nucleoside triphosphate metabolites, and enhanced selectivity over incorporation by mitochondrial RNA and DNA polymerases. Selectivity over the mitochondrial polymerases was found to be extremely sensitive to the specific 4'-substitution and not readily predictable. Combining the most potent and selective 4'-groups from N-nucleoside analogs onto a 2'd2'F C-nucleoside analog resulted in the identification of beta-D-2'-deoxy-2'-alpha-fluoro-4'-alpha-cyano-5-aza-7,9-dideaza adenosine as a promising nucleoside lead for RSV. (C) 2015 Elsevier Ltd. All rights reserved.
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