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uridine-3'-phosphate disodium salt | 35170-03-7

中文名称
——
中文别名
——
英文名称
uridine-3'-phosphate disodium salt
英文别名
3'-uridine monophosphate disodium salt;disodium uridine-3'-monophosphate;uridine 3’-monophosphate disodium salt;[3']uridylic acid ; disodium-salt;[3']Uridylsaeure; Dinatrium-Salz;sodium;[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] phosphate
uridine-3'-phosphate disodium salt化学式
CAS
35170-03-7
化学式
C9H11N2O9P*2Na
mdl
——
分子量
368.148
InChiKey
KWEHEBFOIOLYPP-IAIGYFSYSA-L
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:
    >215°C (dec.)
  • 溶解度:
    PBS(pH 7.2):10 mg/mL

计算性质

  • 辛醇/水分配系数(LogP):
    -6.99
  • 重原子数:
    22.0
  • 可旋转键数:
    4.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    176.97
  • 氢给体数:
    3.0
  • 氢受体数:
    10.0

SDS

SDS:afec1fbc1a0d167e0fd707169dfdd18e
查看

制备方法与用途

用途:用作食品添加剂、基因工程试剂及制药原料。

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Phosphorylation, oligomerization and self-assembly in water under potential prebiotic conditions
    摘要:
    在水的环境下对(前)生物底物进行磷酸化,是生命起源中的关键一步。以往的研究要么成功率有限,要么需要特殊环境,这些环境与后续产生相应寡聚体或更高层次结构不相容。在这里,我们证明了二氨基磷酸盐(DAP)——一种可能的前生物剂,由三聚磷酸盐产生——在不需要缩合剂的情况下,能够有效地在水溶性(溶液/膏状)条件下,对多种(前)生物构建单元(核苷/酸、氨基酸和脂质前体)进行(氨基)磷酸化。值得注意的是,更高层次的结构(寡核苷酸、肽和脂质体)在相同的磷酸化反应条件下形成。这种可能的前生物磷酸化过程在类似的反应条件下,可以在单一的水环境中实现三种(前)生物相关分子的系统化学及其寡聚体。在水中对(前)生物分子进行磷酸化一直是前生物化学长期追求的目标。现在,我们已经证明二氨基磷酸盐在水中对核苷、氨基酸和甘油/脂肪酸进行磷酸化的同时,也在同一反应混合物中形成更高层次的结构,如寡核苷酸、肽和脂质体。
    DOI:
    10.1038/nchem.2878
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 生成 uridine-3'-phosphate disodium salt
    参考文献:
    名称:
    Barker et al., Journal of the Chemical Society, 1949, p. 904,906
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Biotin-phenyldiazomethane conjugates as labeling reagents at phosphate in mono and polynucleotides
    作者:Cécile Bourget、Emmanuelle Trévisiol、Isabelle Bridon、Mitsuharu Kotera、Jean Lhomme、Ali Laayoun
    DOI:10.1016/j.bmc.2004.12.046
    日期:2005.3.1
    Molecules 2-5 that include in their structure a biotin moiety as detectable unit and differently substituted phenyl diazo functions as reactive group were prepared as reagents for labeling the phosphate group in mono and polynucleotides. These molecules were shown to react selectively and quantitatively with the model nucleotide 3'-UMP. They were used successfully in the labeling step of DNA and RNA
    制备在其结构中包括生物素部分作为可检测单元并且不同取代的苯基重氮官能团作为反应性基团的分子2-5,作为标记单和多核苷酸中磷酸基团的试剂。这些分子显示出与模型核苷酸3'-UMP选择性和定量反应。它们已使用高密度DNA芯片(或微阵列)技术成功用于DNA和RNA分析的标记步骤。
  • Synthesis and spectroscopic analysis of branched RNA fragments: messenger RNA splicing intermediates
    作者:Masad J. Damha、Kelvin K. Ogilvie
    DOI:10.1021/jo00251a010
    日期:1988.8
  • Pyrenyldiazomethane, a versatile reagent for nucleotide phosphate alkylation
    作者:Mitsuharu Kotera、Marie-Louise Dheu、Anne Milet、Jean Lhomme、Ali Laayoun
    DOI:10.1016/j.bmcl.2004.11.024
    日期:2005.2
    Pyrenyldiazomethane was shown to react quantitatively and selectively at phosphate with 2'-, 3'-, and 5'-nucleotide phosphates incorporating the different nucleic bases. (C) 2004 Elsevier Ltd. All rights reserved.
  • Phosphorylation, oligomerization and self-assembly in water under potential prebiotic conditions
    作者:Clémentine Gibard、Subhendu Bhowmik、Megha Karki、Eun-Kyong Kim、Ramanarayanan Krishnamurthy
    DOI:10.1038/nchem.2878
    日期:2018.2
    Prebiotic phosphorylation of (pre)biological substrates under aqueous conditions is a critical step in the origins of life. Previous investigations have had limited success and/or require unique environments that are incompatible with subsequent generation of the corresponding oligomers or higher-order structures. Here, we demonstrate that diamidophosphate (DAP)—a plausible prebiotic agent produced from trimetaphosphate—efficiently (amido)phosphorylates a wide variety of (pre)biological building blocks (nucleosides/tides, amino acids and lipid precursors) under aqueous (solution/paste) conditions, without the need for a condensing agent. Significantly, higher-order structures (oligonucleotides, peptides and liposomes) are formed under the same phosphorylation reaction conditions. This plausible prebiotic phosphorylation process under similar reaction conditions could enable the systems chemistry of the three classes of (pre)biologically relevant molecules and their oligomers, in a single-pot aqueous environment. Phosphorylation of (pre)biological molecules in water has been a long-sought goal in prebiotic chemistry. Now, it has been demonstrated that diamidophosphate phosphorylates nucleosides, amino acids and glycerol/fatty acids in aqueous medium, while simultaneously leading to higher-order structures such as oligonucleotides, peptides and liposomes in the same reaction mixture.
    在水的环境下对(前)生物底物进行磷酸化,是生命起源中的关键一步。以往的研究要么成功率有限,要么需要特殊环境,这些环境与后续产生相应寡聚体或更高层次结构不相容。在这里,我们证明了二氨基磷酸盐(DAP)——一种可能的前生物剂,由三聚磷酸盐产生——在不需要缩合剂的情况下,能够有效地在水溶性(溶液/膏状)条件下,对多种(前)生物构建单元(核苷/酸、氨基酸和脂质前体)进行(氨基)磷酸化。值得注意的是,更高层次的结构(寡核苷酸、肽和脂质体)在相同的磷酸化反应条件下形成。这种可能的前生物磷酸化过程在类似的反应条件下,可以在单一的水环境中实现三种(前)生物相关分子的系统化学及其寡聚体。在水中对(前)生物分子进行磷酸化一直是前生物化学长期追求的目标。现在,我们已经证明二氨基磷酸盐在水中对核苷、氨基酸和甘油/脂肪酸进行磷酸化的同时,也在同一反应混合物中形成更高层次的结构,如寡核苷酸、肽和脂质体。
  • Barker et al., Journal of the Chemical Society, 1949, p. 904,906
    作者:Barker et al.
    DOI:——
    日期:——
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同类化合物

腺苷-3’-磷酸 胸苷酰-(3'-5')-胸苷氰基乙基磷酰三酯 胸腺嘧啶脱氧核苷3-单磷酸铵盐水合物 胞啶-3'-单磷酸二钠盐 环(腺苷酰(3'-5')尿苷单磷酸酯) 尿苷酸 尿苷溴乙酰甲醇5'-二磷酸酯 尿苷氯乙酰甲醇5'-二磷酸酯 [(2R,3S,4R,5R)-5-(6-氨基嘌呤-9-基)-4-羟基-2-(羟基甲基)四氢呋喃-3-基]苯基磷酸氢酯 N-苯甲酰基-2'-脱氧-3'-胞苷酸2-氯苯基2-氰基乙基酯 8-[(E)-苄亚基氨基]-2'-脱氧腺苷3'-(磷酸二氢酯) 5-甲基-2'-脱氧胞苷-3'-磷酸 3'-(二氢磷酸)鸟嘌呤核苷 3'-(1-丁基磷酰)腺苷 2ˊ-脱氧胞苷-3ˊ-一磷酸 2-脱氧腺苷-3-单磷酸酯*铵 2'-脱氧鸟苷 3'-(磷酸二氢酯) 2'-脱氧腺苷酰-(3'-5')-2'-脱氧腺苷酰-(3'-5)-2'-脱氧腺苷 2'-脱氧-3'-胞苷酸二钠盐 2' -脱氧3' -磷酸游离酸 uridine 3'-(2,2,2-trichloroethyl)phosphate triethylammonium salt 5'-O-pivaloyl-2'-O-(tetrahydropyran-2-yl)uridin-3'-yl 2,2-difluoroethyl isopropyl phosphate 3'-O-(di-tert-butoxyphosphoryl)-6-N-benzoyladenosine 2',5'-di-O-tert-butyldimethylsilyluridine 3'-(2,2,2-trichloroethyl)phosphate α-L-threofuranosyl adenine-3′-monophosphate α-L-threofuranosyl thymine-3′-monophosphate N2-2-nitrobenzen-1-yl-2'-deoxyguanosine-3'-phosphate thymidine 3'-monophosphate 3'-(5'-deoxy-5-fluoro)uridylic acid mono[(2R)-2,3-dihydroxypropyl] ester guanosyl-(3',3')-uridine thymidine 3'-hexadecylphosphate Thymidine 3'-(1,2-dimyristoyl-sn-glycero-3-phosphate) Diethyl 5'-O-(tert-butyldimethylsilyl)-N6,N6-diethyl-2'-deoxyadenosine 3'-phosphate 9-β-D-Arabinofuranosylhypoxanthine-3'-phosphate 3'-Cytidylic acid, N-benzoyl-2'-deoxy-5'-O-(9-phenyl-9H-xanthen-9-yl)-, mono(2-chlorophenyl) ester Niacinamide adenylate 2'-deoxyadenosine-3'-triphosphate dCpdU 1-(O3-phosphono-β-D-arabinofuranosyl)-1H-pyrimidine-2,4-dione 2',5'-Di(tert-butyldimethylsilyl)-3'-(ethyl 4-(hydroxymethyl)phenyl phosphate)uridine 2',5'-Di(tert-butyldimethylsilyl)-3'-(ethyl 4-formylphenyl phosphate)uridine 2',5'-Di(tert-butyldimethylsilyl)-3'-(ethyl vinyl phosphate)uridine 2',5'-Di(tert-butyldimethylsilyl)-3'-(ethyl 4-(fluoromethyl)phenyl phosphate)uridine Phosphoric acid (2R,3R,4R,5R)-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 1,2-dibromo-ethyl ester ethyl ester N(6)-(benzoyl)-2'-O-(tert-butyldimethylsilyl)adenosine 3'-(allyl 2-cyanoethyl phosphate) N6-benzoyl-3'-O-[bis(benzyloxy)phosphoryl]-2'-O-(4-methoxybenzyl)adenosine 2'-deoxyguanosine 3'-monophosphate ammonium salt Phosphoric acid dibenzyl ester (2R,3S,5R)-2-hydroxymethyl-5-(6-methylamino-purin-9-yl)-tetrahydro-furan-3-yl ester N6-methyl-2'-deoxyadenosine-3'-phosphate [(2R,3S,5R)-3-[(2,2-dicyano-3-hydroxypropoxy)-(2-methoxyethoxy)phosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl 2,2-dimethylpropanoate