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p-hydroxyphenylacetaldehyde oxime | 70365-10-5

中文名称
——
中文别名
——
英文名称
p-hydroxyphenylacetaldehyde oxime
英文别名
Tyramine oxime (E);4-hydroxyphenylacetaldoxime;p-hydroxyphenylacetaldoxime;anti-4-Hydroxy-phenylacetaldehyd-oxim, Anti-Verb.;4-[(2E)-2-hydroxyiminoethyl]phenol
p-hydroxyphenylacetaldehyde oxime化学式
CAS
70365-10-5
化学式
C8H9NO2
mdl
——
分子量
151.165
InChiKey
TVXJJNJGTDWFLD-RMKNXTFCSA-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:
    358.8±25.0 °C(Predicted)
  • 密度:
    1.14±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    52.8
  • 氢给体数:
    2
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Dhurrin Synthesis in Sorghum Is Regulated at the Transcriptional Level and Induced by Nitrogen Fertilization in Older Plants
    摘要:
    摘要

    高粱(Sorghum bicolor L. Moench)中的氰糖苷dhurrin的含量取决于植物的年龄和生长条件。在发芽后不久,氰化物潜力最高。在这个阶段,氮肥的施用对dhurrin含量没有影响,而在较老的植物中,氮肥的施用会引起增加。在所有阶段,dhurrin的含量与两种生物合成酶CYP79A1和CYP71E1的活性以及这两种酶的蛋白质和mRNA水平密切相关。在发育过程中,CYP79A1的活性低于CYP71E1的活性,这表明CYP79A1催化dhurrin合成的速率限制步骤,这与使用暗化的幼苗已经显示的结果一致。dhurrin合成的位置在植物发育过程中从叶子转移到茎。综合结果表明,高粱中的dhurrin含量主要由生物合成酶CYP79A1和CYP71E1的转录调控决定。

    DOI:
    10.1104/pp.000687
  • 作为产物:
    描述:
    4-羟基苯乙酸甲酯盐酸羟胺sodium acetate二异丁基氢化铝 作用下, 以 乙醇甲苯 为溶剂, 反应 11.0h, 生成 p-hydroxyphenylacetaldehyde oxime
    参考文献:
    名称:
    探索十字花科植物的真菌病原体中关键的代谢途径:吲哚-3-乙醛肟,4-羟苯基乙醛肟及其代谢物的生物转化。
    摘要:
    吲哚-3-乙醛肟是十字花科植物不同植物次生代谢产物生物合成中至关重要的中间体。在十字花科植物中引起重要植物病的真菌,吲哚-3-乙醛肟经吲哚-3-乙腈代谢为吲哚-3-乙酸,黄斑病的致病性黑斑病致病因子,黑腿病的致病因子,茄根枯菌的致病因子描述了根腐病和干腐病的核盘菌菌核病病原体。同样,还报道了吲哚-3-乙醛肟和代谢物的抗真菌活性以及相同植物病原体和昆虫真菌病原体球孢白僵菌对4-羟基苯基乙醛肟的合成和生物转化。
    DOI:
    10.1016/s0968-0896(03)00241-4
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文献信息

  • Cytochrome P450 monooxygenases
    申请人:——
    公开号:US20030041346A1
    公开(公告)日:2003-02-27
    Cytochrome P450 II dependent monooxygenases and DNA molecules encoding these monooxygenases are provided, which are able to catalyze the biosynthethic conversion of aldoximes to nitrils and the conversion of said nitrils to the corresponding cyanohydrins, which are the presursors of cyanogenic glycosides. Moreover, the invention provides methods for obtaining DNA molecules according to the invention and methods for obtaining transgenic plants resistant to insects, acarids, or nematodes or plants with improved nutritive value.
    本发明提供了依赖于细胞色素P450II的单加氧酶和编码这些单加氧酶的DNA分子,这些单加氧酶能够催化醛肟的生物合成转化为腈和将所述腈转化为相应的氰醇,这些是青霉素糖苷的前体。此外,本发明还提供了根据本发明获得DNA分子的方法和获得对昆虫、螨虫或线虫具有抗性或具有改善营养价值的转基因植物的方法。
  • P450 Monooxygenases of the cyp79 family
    申请人:——
    公开号:US20030166202A1
    公开(公告)日:2003-09-04
    The invention provides DNA coding for cytochrome P450 monooxygenases of the CYP79 family catalyzing the conversion of an aliphatic or aromatic amino acid or chain-elongated methionine homologue to the corresponding oxime. Preferred embodiments of the invention are enzymes catalyzing the conversion of L-Valine and L-Isoleucine such as the cassava enzymes CYP79D1 and CYP79D2, enzymes catalyzing the conversion of tyrosine such as the Triglochin maritima enzymes CYP79E1 and CYP79E2, enzymes catalyzing the conversion of tryptophan to the corresponding oxime indole-3-acetaldoxime such as the Arabidopsis thaliana enzyme CYP79A2 and the Brassica napus enzyme CYP79B5, and enzymes catalyzing the conversion of a chain-elongated methionine homologue such as the Arabidopsis thaliana enzymes CYP79F1 and CYP79F2. Transgenic expression of said DNA or parts thereof in plants can be used to manipulate the biosynthesis of corresponding glucosinolates or cyanogenic glucosides.
    该发明提供了编码CYP79家族细胞色素P450单加氧酶的DNA,其催化将脂肪族或芳香族氨基酸或链延长的蛋氨酸同源物转化为相应的肟类。该发明的优选实施例是催化L-缬氨酸和L-异亮氨酸转化的酶,例如木薯酶CYP79D1和CYP79D2,催化酪氨酸转化的Triglochin maritima酶CYP79E1和CYP79E2,催化色氨酸转化为相应的肟类吲哚-3-乙醛肟的Arabidopsis thaliana酶CYP79A2和Brassica napus酶CYP79B5,以及催化链延长的蛋氨酸同源物转化的Arabidopsis thaliana酶CYP79F1和CYP79F2。在植物中转基因表达该DNA或其部分可以用于操纵相应的硫代葡萄糖苷或氰基葡萄糖苷的生物合成。
  • Dhurrin Synthesis in Sorghum Is Regulated at the Transcriptional Level and Induced by Nitrogen Fertilization in Older Plants
    作者:Peter Kamp Busk、Birger Lindberg Møller
    DOI:10.1104/pp.000687
    日期:2002.7.1
    Abstract

    The content of the cyanogenic glucoside dhurrin in sorghum (Sorghum bicolor L. Moench) varies depending on plant age and growth conditions. The cyanide potential is highest shortly after onset of germination. At this stage, nitrogen application has no effect on dhurrin content, whereas in older plants, nitrogen application induces an increase. At all stages, the content of dhurrin correlates well with the activity of the two biosynthetic enzymes, CYP79A1 and CYP71E1, and with the protein and mRNA level for the two enzymes. During development, the activity of CYP79A1 is lower than the activity of CYP71E1, suggesting that CYP79A1 catalyzes the rate-limiting step in dhurrin synthesis as has previously been shown using etiolated seedlings. The site of dhurrin synthesis shifts from leaves to stem during plant development. In combination, the results demonstrate that dhurrin content in sorghum is largely determined by transcriptional regulation of the biosynthetic enzymes CYP79A1 and CYP71E1.

    摘要

    高粱(Sorghum bicolor L. Moench)中的氰糖苷dhurrin的含量取决于植物的年龄和生长条件。在发芽后不久,氰化物潜力最高。在这个阶段,氮肥的施用对dhurrin含量没有影响,而在较老的植物中,氮肥的施用会引起增加。在所有阶段,dhurrin的含量与两种生物合成酶CYP79A1和CYP71E1的活性以及这两种酶的蛋白质和mRNA水平密切相关。在发育过程中,CYP79A1的活性低于CYP71E1的活性,这表明CYP79A1催化dhurrin合成的速率限制步骤,这与使用暗化的幼苗已经显示的结果一致。dhurrin合成的位置在植物发育过程中从叶子转移到茎。综合结果表明,高粱中的dhurrin含量主要由生物合成酶CYP79A1和CYP71E1的转录调控决定。

  • Metabolic engineering of dhurrin in transgenic <i>Arabidopsis</i> plants with marginal inadvertent effects on the metabolome and transcriptome
    作者:Charlotte Kristensen、Marc Morant、Carl Erik Olsen、Claus T. Ekstrøm、David W. Galbraith、Birger Lindberg Møller、Søren Bak
    DOI:10.1073/pnas.0409233102
    日期:2005.2

    Focused and nontargeted approaches were used to assess the impact associated with introduction of new high-flux pathways in Arabidopsis thaliana by genetic engineering. Transgenic A. thaliana plants expressing the entire biosynthetic pathway for the tyrosine-derived cyanogenic glucoside dhurrin as accomplished by insertion of CYP79A1 , CYP71E1 , and UGT85B1 from Sorghum bicolor were shown to accumulate 4% dry-weight dhurrin with marginal inadvertent effects on plant morphology, free amino acid pools, transcriptome, and metabolome. In a similar manner, plants expressing only CYP79A1 accumulated 3% dry weight of the tyrosine-derived glucosinolate, p -hydroxybenzylglucosinolate with no morphological pleitropic effects. In contrast, insertion of CYP79A1 plus CYP71E1 resulted in stunted plants, transcriptome alterations, accumulation of numerous glucosides derived from detoxification of intermediates in the dhurrin pathway, and in loss of the brassicaceae-specific UV protectants sinapoyl glucose and sinapoyl malate and kaempferol glucosides. The accumulation of glucosides in the plants expressing CYP79A1 and CYP71E1 was not accompanied by induction of glycosyltransferases, demonstrating that plants are constantly prepared to detoxify xenobiotics. The pleiotrophic effects observed in plants expressing sorghum CYP79A1 and CYP71E1 were complemented by retransformation with S. bicolor UGT85B . These results demonstrate that insertion of high-flux pathways directing synthesis and intracellular storage of high amounts of a cyanogenic glucoside or a glucosinolate is achievable in transgenic A. thaliana plants with marginal inadvertent effects on the transcriptome and metabolome.

    采用有针对性和非有针对性的方法,评估了通过基因工程引入新的高通量途径对拟南芥的影响。表达了源自高粱的整个酪氨酸衍生的氰甙dhurrin的生物合成途径,包括插入了CYP79A1、CYP71E1和UGT85B1,的转基因拟南芥植物被证明可以积累4%的dhurrin干重,对植物形态、游离氨基酸池、转录组和代谢组的不良影响微乎其微。同样,只表达CYP79A1的植物可以积累3%的酪氨酸衍生的糖苷,即p-羟基苯甲醇糖苷,没有形态多向性影响。相比之下,插入CYP79A1和CYP71E1会导致矮化的植物、转录组改变、积累许多源自dhurrin途径中间产物解毒的糖苷,以及失去十字花科特有的紫外线保护剂芥子酰葡萄糖和芥子酰苹果酸和卡培菲糖苷。表达CYP79A1和CYP71E1的植物中糖苷的积累并未伴随着糖基转移酶的诱导,表明植物始终准备解毒外源物质。通过重新转化S.bicolor UGT85B,可以补充表达高粱CYP79A1和CYP71E1的植物中观察到的多向性效应。这些结果表明,在转基因拟南芥植物中插入定向合成和细胞内储存大量氰甙或糖苷的高通量途径是可行的,对转录组和代谢组的不良影响微乎其微。
  • A method of producing a low molecular weight organic compound in a cell
    申请人:Poalis A/S
    公开号:EP1510586A1
    公开(公告)日:2005-03-02
    A method of producing a low molecular weight organic compound (e.g. a plant or bacteria secondary metabolite) in increased yields involving use of a cell (e.g. a plant or microorganism cell), which comprises a gene involved in the biosynthesis pathway leading to a low molecular weight organic aglycon compound and a glycosyltransferase gene capable of glycosylating the produced aglycon.
    一种提高低分子量有机化合物(如植物或细菌的次级代谢产物)产量的方法,涉及使用细胞(如植物或微生物细胞),该细胞包括一个参与导致低分子量有机苷元化合物的生物合成途径的基因和一个能够将所产生的苷元糖基化的糖基转移酶基因。
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