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eriodictyol 7-neohesperidoside | 13241-32-2

中文名称
——
中文别名
——
英文名称
eriodictyol 7-neohesperidoside
英文别名
eriodictyol 7-O-neohesperidoside;neoeriocitrin;β-Neohesperidosyl-7 tetrahydroxy-3',4',5,7 flavanon; β-Neohesperidosid-7 des Eriodictyol;3',4',5-Trihydroxy-7-neohesperidosyl-flavanon;(S)-3',4',5,7-Tetrahydroxyflavanone-7-[2-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside];7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-2,3-dihydrochromen-4-one
eriodictyol 7-neohesperidoside化学式
CAS
13241-32-2
化学式
C27H32O15
mdl
——
分子量
596.542
InChiKey
OBKKEZLIABHSGY-BEDUMGIKSA-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:
    277°C
  • 沸点:
    960.7±65.0 °C(Predicted)
  • 密度:
    1.73±0.1 g/cm3 (20 ºC 760 Torr)
  • 溶解度:
    溶于甲醇;
  • LogP:
    2.130 (est)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    42
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    245
  • 氢给体数:
    9
  • 氢受体数:
    15

安全信息

  • WGK Germany:
    3
  • 海关编码:
    29389090

制备方法与用途

生物活性 Neoeriocitrin 从百日草(Drynaria Rhizome)中分离而出,在 MC3T3-E1 细胞系中表现出对增殖和成骨分化的影响。Neoeriocitrin 还是一种有效的乙酰胆碱酯酶抑制剂。

化学性质:Neoeriocitrin 是一种白色结晶粉末,可溶于甲醇、乙醇、DMSO 等有机溶剂,并来源于柑橘。

文献信息

  • METHOD FOR THE BIOTECHNOLOGICAL PRODUCTION OF FLAVONE GLYCOSIDE DIHYDROCHALCONES
    申请人:Symrise AG
    公开号:US20180216152A1
    公开(公告)日:2018-08-02
    The invention relates to a method for producing flavone glycoside dihydrochalcones, having the following steps: (a) providing a transgenic microorganism containing (i) a first nucleic acid portion (A) containing a gene which codes for a bacterial chalcone isomerase and (ii) a second nucleic acid portion (B) containing a gene which codes for a bacterial enoate reductase, (b) adding one or more flavone glycosides to the transgenic microorganism under conditions which allow the simultaneous isomerization and reduction of the flavone glycoside into the flavone glycoside dihydrochalcone, and optionally (d) isolating and purifying the final product, wherein the nucleic acid portion (A) (1) is a nucleotide sequence according to SEQ ID NO:1, in which the nucleic acid portion (A′) according to SEQ ID NO:3 has been cut out, or (2) is an amino acid sequence according to SEQ ID NO:2, in which the amino acid portion (A′) according to SEQ ID NO:4 has been cut out.
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