Indole-3-acetyl-myo-inositol (BioDeep_00000005338)

 

Secondary id: BioDeep_00000898447

human metabolite Endogenous


代谢物信息卡片


(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl 2-(1H-indol-3-yl)acetate

化学式: C16H19NO7 (337.1161464)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(plant) 36.42%

分子结构信息

SMILES: C1=CC=C2C(=C1)C(=CN2)CC(=O)OC3C(C(C(C(C3O)O)O)O)O
InChI: InChI=1S/C16H19NO7/c18-10(5-7-6-17-9-4-2-1-3-8(7)9)24-16-14(22)12(20)11(19)13(21)15(16)23/h1-4,6,11-17,19-23H,5H2/t11?,12-,13+,14+,15-,16?

描述信息

1H-Indol-3-ylacetyl-myo-inositol is found in cereals and cereal products. 1H-Indol-3-ylacetyl-myo-inositol is present in Oryza sativa (rice) and Zea mays (corn
Present in Oryza sativa (rice) and Zea mays (corn). 1H-Indol-3-ylacetyl-myo-inositol is found in cereals and cereal products, rice, and corn.

同义名列表

10 个代谢物同义名

(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl 2-(1H-indol-3-yl)acetate; (1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl 1H-indol-3-ylacetate; 1D-1-O-(indol-3-yl)acetyl-myo-inositol; 1H-Indol-3-ylacetyl-myo-inositol; indol-3-Ylacetyl-1D-myo-inositol; Indole-3-acetyl-1D-myo-inositol; Indole-3-ylacetyl-myo-inositol; indol-3-Ylacetyl-myo-inositol; Indole-3-acetyl-myo-inositol; Iaa-inositol



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

2 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。



文献列表

  • Maciej Ostrowski, Anna Ciarkowska, Agata Dalka, Emilia Wilmowicz, Anna Jakubowska. Biosynthesis pathway of indole-3-acetyl-myo-inositol during development of maize (Zea mays L.) seeds. Journal of plant physiology. 2020 Feb; 245(?):153082. doi: 10.1016/j.jplph.2019.153082. [PMID: 31862648]
  • Tongbo Wu, Yuan Liang, Xiaocui Zhu, Meiping Zhao, Huwei Liu. Separation and quantification of four isomers of indole-3-acetyl-myo-inositol in plant tissues using high-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. Analytical and bioanalytical chemistry. 2014 May; 406(13):3239-47. doi: 10.1007/s00216-014-7739-2. [PMID: 24633567]
  • W Domagalski, A Schulze, R S Bandurski. Isolation and characterization of esters of indole-3-acetic acid from the liquid endosperm of the horse chestnut (Aesculus species). Plant physiology. 1987; 84(?):1107-13. doi: 10.1104/pp.84.4.1107. [PMID: 11539676]
  • R S Bandurski, A Schulze, Y Momonoki. Gravity-induced asymmetric distribution of a plant growth hormone. The Physiologist. 1984; 27(6 Suppl):S123-6. doi: . [PMID: 11539003]
  • J R Chisnell. Myo-inositol esters of indole-3-acetic acid are endogenous components of Zea mays L. shoot tissue. Plant physiology. 1984; 74(?):278-83. doi: 10.1104/pp.74.2.278. [PMID: 11540816]
  • . . . . doi: . [PMID: 11539037]
  • . . . . doi: . [PMID: 11539040]