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(3R,4S)-5-fluoro-5-deoxy-D-ribulose-1-phosphate | 953394-51-9

中文名称
——
中文别名
——
英文名称
(3R,4S)-5-fluoro-5-deoxy-D-ribulose-1-phosphate
英文别名
5-fluoro-5-deoxy-d-ribulose 1-phosphate;[(3R,4S)-5-fluoro-3,4-dihydroxy-2-oxopentyl] dihydrogen phosphate
(3R,4S)-5-fluoro-5-deoxy-D-ribulose-1-phosphate化学式
CAS
953394-51-9
化学式
C5H10FO7P
mdl
——
分子量
232.102
InChiKey
RGVDXIXIXWVTIL-NQXXGFSBSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    -2.7
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    124
  • 氢给体数:
    4
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    (3R,4S)-5-fluoro-5-deoxy-D-ribulose-1-phosphate 在 phytase from Aspergillus ficuum P 9792 作用下, 反应 16.0h, 生成 5-fluoro-5-deoxy-D-ribulose
    参考文献:
    名称:
    The identification of (3R,4S)-5-fluoro-5-deoxy-d-ribulose-1-phosphate as an intermediate in fluorometabolite biosynthesis in Streptomyces cattleya
    摘要:
    (3R,4S)-5-氟-5-脱氧-D-核糖醇-1-磷酸酯(5-FDRulP)在链霉菌cattleya的氟乙酸和4-氟苏氨酸生物合成途径中被鉴定为第三个含氟的中间体。5-FDRulP是在5'-氟-5'-脱氧腺苷(5'-FDA)形成之后,由嘌呤核苷磷酸化酶作用使5'-FDA发生磷酸水解生成5-氟-5-脱氧-D-核糖-1-磷酸(5-FDRP),随后通过异构酶的作用将5-FDRP转化为5-FDRulP。5-FDRulP的(3R,4S)异构体身份通过比较F-19{H-1} NMR研究得以确定。具体来说,链霉菌cattleya细胞提取物中积累的5-FDRulP经磷酸酶处理生成非磷酸化糖5-氟-5-脱氧-D-核糖醇(5-FDRul)。该链霉菌cattleya产物与体外生物转化产物进行比较,其中5-氟-5-脱氧-D-核糖和5-氟-5-脱氧-D-木糖分别在葡萄糖异构酶作用下转化为5-氟-5-脱氧-D-核糖醇和5-氟-5-脱氧-D-木糖醇。结果表明,5-氟-5-脱氧-D-核糖生成了与5-FDRulP中相同的异构体。 © 2007 Elsevier Inc. 保留所有权利。
    DOI:
    10.1016/j.bioorg.2007.04.001
  • 作为产物:
    描述:
    5'-fluoro-5'-deoxy-D-ribose-1-phosphate 在 乙二胺四乙酸 作用下, 反应 16.0h, 生成 (3R,4S)-5-fluoro-5-deoxy-D-ribulose-1-phosphate
    参考文献:
    名称:
    The identification of (3R,4S)-5-fluoro-5-deoxy-d-ribulose-1-phosphate as an intermediate in fluorometabolite biosynthesis in Streptomyces cattleya
    摘要:
    (3R,4S)-5-氟-5-脱氧-D-核糖醇-1-磷酸酯(5-FDRulP)在链霉菌cattleya的氟乙酸和4-氟苏氨酸生物合成途径中被鉴定为第三个含氟的中间体。5-FDRulP是在5'-氟-5'-脱氧腺苷(5'-FDA)形成之后,由嘌呤核苷磷酸化酶作用使5'-FDA发生磷酸水解生成5-氟-5-脱氧-D-核糖-1-磷酸(5-FDRP),随后通过异构酶的作用将5-FDRP转化为5-FDRulP。5-FDRulP的(3R,4S)异构体身份通过比较F-19{H-1} NMR研究得以确定。具体来说,链霉菌cattleya细胞提取物中积累的5-FDRulP经磷酸酶处理生成非磷酸化糖5-氟-5-脱氧-D-核糖醇(5-FDRul)。该链霉菌cattleya产物与体外生物转化产物进行比较,其中5-氟-5-脱氧-D-核糖和5-氟-5-脱氧-D-木糖分别在葡萄糖异构酶作用下转化为5-氟-5-脱氧-D-核糖醇和5-氟-5-脱氧-D-木糖醇。结果表明,5-氟-5-脱氧-D-核糖生成了与5-FDRulP中相同的异构体。 © 2007 Elsevier Inc. 保留所有权利。
    DOI:
    10.1016/j.bioorg.2007.04.001
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文献信息

  • The identification of (3R,4S)-5-fluoro-5-deoxy-d-ribulose-1-phosphate as an intermediate in fluorometabolite biosynthesis in Streptomyces cattleya
    作者:Mayca Onega、Ryan P. McGlinchey、Hai Deng、John T.G. Hamilton、David O’Hagan
    DOI:10.1016/j.bioorg.2007.04.001
    日期:2007.10
    (3R,4S)-5-Fluoro-5-deoxy-D-ribulose-1-phosphate (5-FDRulP) has been identified as the third fluorinated intermediate on the biosynthetic pathway to fluoroacetate and 4-fluorothreonine in Streptomyces cattleya. 5-FDRulP is generated after formation of 5 '-fluoro-5 '-deoxyadenosine (5 '-FDA) and then phosphorolysis of 5 '-FDA to 5-fluoro-5-deoxy-D-ribose-1-phosphate (5-FDRP) by the action of a purine nucleoside phosphorylase. An isomerase mediates the conversion of 5-FDRP to 5-FDRulP. The identity of the (3R,4S) diastereoisomer of 5-FDRulP was established by comparative F-19H-1} NMR studies whereby 5-FDRulP that accumulated in a cell free extract of S. cattleya, was treated with a phytase to generate the non-phosphorylated sugar, 5-fluoro-5-deoxy-D-ribulose (5-FDRul). This S. cattleya product was compared to the product of an in-vitro biotransformation where separately 5-fluoro5-deoxy-D-ribose and 5-fluoro-5-deoxy-D-xylose were converted to 5-fluoro-5-deoxy-D-ribulose and 5-fluoro-5-deoxy-D-xylulose respectively by the action of glucose isomerase. It was demonstrated that 5-fluoro-5-deoxy-D-ribose gave the identical diastereoisomer to that observed from 5-FDRulP. (c) 2007 Elsevier Inc. All rights reserved.
    (3R,4S)-5-氟-5-脱氧-D-核糖醇-1-磷酸酯(5-FDRulP)在链霉菌cattleya的氟乙酸和4-氟苏氨酸生物合成途径中被鉴定为第三个含氟的中间体。5-FDRulP是在5'-氟-5'-脱氧腺苷(5'-FDA)形成之后,由嘌呤核苷磷酸化酶作用使5'-FDA发生磷酸水解生成5-氟-5-脱氧-D-核糖-1-磷酸(5-FDRP),随后通过异构酶的作用将5-FDRP转化为5-FDRulP。5-FDRulP的(3R,4S)异构体身份通过比较F-19H-1} NMR研究得以确定。具体来说,链霉菌cattleya细胞提取物中积累的5-FDRulP经磷酸酶处理生成非磷酸化糖5-氟-5-脱氧-D-核糖醇(5-FDRul)。该链霉菌cattleya产物与体外生物转化产物进行比较,其中5-氟-5-脱氧-D-核糖和5-氟-5-脱氧-D-木糖分别在葡萄糖异构酶作用下转化为5-氟-5-脱氧-D-核糖醇和5-氟-5-脱氧-D-木糖醇。结果表明,5-氟-5-脱氧-D-核糖生成了与5-FDRulP中相同的异构体。 © 2007 Elsevier Inc. 保留所有权利。
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