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N-CBZ胞嘧啶乙酸 | 144564-95-4

中文名称
N-CBZ胞嘧啶乙酸
中文别名
——
英文名称
[N4-(benzyloxycarbonyl)cytosine-1-yl]acetic acid
英文别名
2-Oxo-4-[(benzyloxycarbonyl)amino]pyrimidine-1(2H)-acetic acid;2-[2-oxo-4-(phenylmethoxycarbonylamino)pyrimidin-1-yl]acetic acid
N-CBZ胞嘧啶乙酸化学式
CAS
144564-95-4
化学式
C14H13N3O5
mdl
MFCD01830832
分子量
303.274
InChiKey
ONHBSJOXWOGKOD-UHFFFAOYSA-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

  • 熔点:
    272-274 °C(Solv: methanol (67-56-1))
  • 密度:
    1.39±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    108
  • 氢给体数:
    2
  • 氢受体数:
    5

安全信息

  • 危险性防范说明:
    P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P340,P330,P363,P501
  • 危险性描述:
    H302,H312,H332

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    N-CBZ胞嘧啶乙酸sodium hydroxideN,N-二异丙基乙胺 、 bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 24.5h, 生成 Nα-[[4-N-(benzyloxycarbonyl)cytosin-1-yl]acetyl]-NG-(2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-sulfonyl)-L-arginine
    参考文献:
    名称:
    Neamine derivatives having a nucleobase with a lysine or an arginine as a linker, their synthesis and evaluation as potential inhibitors for HIV TAR–Tat
    摘要:
    Neamine derivatives hearing a nucleobase, adenine, cytosine. guanine or thymine with a lysine or an arginine as a linker have been synthesized and its potential as the inhibitor for HIV TAR-Tat interaction examined. Among them, modified neamine having an arginine-nucleobase showed a higher inhibition than that of the one having a lysine-nuclcobase. The difference of the nucleobase anchor did not characterize inhibition specificity. Also, stereochemistry of the amino acid in the compounds causes no difference in the inhibition for TAR-Tat. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.11.056
  • 作为产物:
    描述:
    1-ethoxycarbonylmethylcytosine4-二甲氨基吡啶 、 sodium hydroxide 作用下, 以 1,4-二氧六环二氯甲烷 为溶剂, 反应 10.0h, 生成 N-CBZ胞嘧啶乙酸
    参考文献:
    名称:
    双面肽核酸:高胸腺嘧啶-同胞嘧啶双峰Cα-PNA(bm - Cα -PNA)形成bm -PNA 2的双链体:DNA Triplex
    摘要:
    Cα-双峰肽核酸(bm - Cα- PNA)是具有两个面的PNA,被设计为PNA的同源物,其中标准PNA骨架中的每个氨基乙基甘氨酸(aeg)重复单元在Cα处通过带有一个三唑接头。这种具有混合序列的bm -Cα-PNA可通过同时与两个互补DNA结合而形成双链体,两个互补DNA分别与t-酰胺侧的碱基序列结合,而另一个与Cα侧链的碱基结合。bm -Cα-PNA的合成,在叔酰胺面上有高胸腺嘧啶(T 7)和高胞嘧啶(C 5通过三唑接头在Cα侧链上的固相合成是通过固相合成和整体点击反应实现的。在互补DNA DA的存在8和DG 6在中性pH下,BM -Cα-PNA 1所形成高阶一个五聚体组成的三链体的双双工2 BM -Cα-PNA-C 5:dG的5个构建在核心双链(BM -Cα-PNA-T 7)2:DA 8三层 圆二色性研究表明,组装可以通过首先进行三重结合,然后通过双面进行,反之亦然。等温滴定量热法数
    DOI:
    10.1021/acs.joc.0c02158
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文献信息

  • [EN] PNA MONOMER AND PRECURSOR<br/>[FR] MONOMERE ET PRECURSEUR PNA
    申请人:PANAGENE INC
    公开号:WO2003091231A1
    公开(公告)日:2003-11-06
    This application relates to monomers of the general formula (I) for the preparation PNA (peptide nucleic acid) oligomers and provides method for the synthesis of both predefined sequence PNA oligomers and random sequence PNA oligomers: (I) wherein E is nitrogen or C-R'; J is sulfur or oxygen; R', Rl, R2, R3, R4 is independently H, halogen, alkyl, nitro, nitrile, alkoxy, halogenated alkyl, halogenated alkoxy, phenyl or halogenated phenyl, RS is H or protected or unprotected side chain of natural or unnatural a-amino acid; and B is a natural or unnatural nucleobase, wherein when said nucleobase has an exocyclic amino function, said function is protected by protecting group which is labile to acids but stable to weak to medium bases in the presence of thiol.
    该应用程序涉及通用式(I)的单体,用于制备PNA(肽核酸)寡聚体,并提供了合成预定义序列PNA寡聚体和随机序列PNA寡聚体的方法:(I)其中E为氮或C-R'; J为硫或氧; R',Rl,R2,R3,R4独立地为H,卤素,烷基,硝基,腈基,烷氧基,卤代烷基,卤代烷氧基,苯基或卤代苯基,RS为H或天然或非天然α-氨基酸的保护或未保护侧链; B为天然或非天然核碱基,其中当所述核碱基具有外环氨基功能时,所述功能由对酸敏感但在巯基存在下对弱到中等碱稳定的保护基保护。
  • PNA monomer and precursor
    申请人:——
    公开号:US20030225252A1
    公开(公告)日:2003-12-04
    This application relates to monomers of the general formula (I) for the preparation of PNA (peptide nucleic acid) oligomers and provides method for the synthesis of both predefined sequence PNA oligomers and random sequence PNA oligomers: 1 wherein E is nitrogen or C—R′; J is sulfur or oxygen; R′, R1, R2, R3, R4 is independently H, halogen, alkyl, nitro, nitrile, alkoxy, halogenated alkyl, halogenated alkoxy, phenyl or halogenated phenyl, R5 is H or protected or unprotected side chain of natural or unnatural &agr;-amino acid; and B is a natural or unnatural nucleobase, wherein when said nucleobase has an exocyclic amino function, said function is protected by protecting group which is labile to acids but stable to weak to medium bases in the presence of thiol.
    该应用程序涉及通式(I)的单体,用于制备PNA(肽核酸)寡聚体,并提供了合成预定义序列PNA寡聚体和随机序列PNA寡聚体的方法: 其中 E为氮或C—R′;J为硫或氧; R′、R1、R2、R3、R4独立地为H、卤素、烷基、硝基、腈基、烷氧基、卤代烷基、卤代烷氧基、苯基或卤代苯基, R5为H或天然或非天然α-氨基酸的保护或未保护侧链;以及 B为天然或非天然核碱基,其中当所述核碱基具有外环氨基功能时,所述功能由对酸敏感但在巯基存在下对弱到中等碱稳定的保护基保护。
  • Peptide nucleic acids having 2,6-diaminopurine nucleobases
    申请人:——
    公开号:US06414112B1
    公开(公告)日:2002-07-02
    A novel class of compounds, known as peptide nucleic acids, bind complementary DNA and RNA strands more strongly than a corresponding DNA strand, and exhibit increased sequence specificity and binding affinity. The peptide nucleic acids of the invention comprise ligands selected from a group consisting of naturally-occurring nucleobases and non-naturally-occurring nucleobases attached to a polyamide backbone. Some PNAs of the invention also contain C1-C8 alkylamine side chains.
    一种新型化合物类别,被称为肽核酸,比相应的DNA链和RNA链结合更牢固,并表现出增强的序列特异性和结合亲和力。该发明的肽核酸包括从天然存在的核碱基和连接到聚酰胺骨架的非天然核碱基中选择的配体。该发明的一些肽核酸还包含C1-C8烷基胺侧链。
  • Peptide nucleic acids
    申请人:——
    公开号:US05539082A1
    公开(公告)日:1996-07-23
    A novel class of compounds, known as peptide nucleic acids, bind complementary ssDNA and RNA strands more strongly than a corresponding DNA. The peptide nucleic acids generally comprise ligands such as naturally occurring DNA bases attached to a peptide backbone through a suitable linker.
    一种新型化合物,被称为肽核酸,比相应的DNA更强烈地结合互补的单链DNA和RNA链。肽核酸通常包括配体,例如天然存在的DNA碱基,通过适当的连接剂连接到肽骨架上。
  • Peptide nucleic acids having enhanced binding affinity, sequence
    申请人:——
    公开号:US05714331A1
    公开(公告)日:1998-02-03
    A novel class of compounds, known as peptide nucleic acids, bind complementary DNA and RNA strands more strongly than a corresponding DNA strand, and exhibit increased sequence specificity and solubility. The peptide nucleic acids comprise ligands selected from a group consisting of naturally-occurring nucleobases and non-naturally-occurring nucleobases attached to a polyamide backbone, and contain C.sub.1 -C.sub.8 alkylamine side chains. Methods of enhancing the solubility, binding affinity and sequence specificity of PNAs are provided.
    一种新型化合物,被称为肽核酸,比相应的DNA链和RNA链结合更牢固,并表现出增强的序列特异性和溶解性。肽核酸包括从天然存在的核碱基和连接到聚酰胺骨架的非天然存在的核碱基中选择的配体,并含有C.sub.1 -C.sub.8烷基胺侧链。提供了增强PNAs溶解性、结合亲和力和序列特异性的方法。
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