Luteoforol (BioDeep_00000005991)

 

Secondary id: BioDeep_00000270472, BioDeep_00001869637

human metabolite PANOMIX_OTCML-2023 PANOMIX-Anthocyanidin natural product


代谢物信息卡片


2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4,5,7-triol, 9ci

化学式: C15H14O6 (290.079)
中文名称: 3-去氧鲁考 矢车菊素
谱图信息: 最多检出来源 Viridiplantae(plant) 18.23%

分子结构信息

SMILES: C1C(C2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O)O
InChI: InChI=1S/C15H14O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,12-13,16-20H,6H2

描述信息

Constituent of Zea mays (sweet corn) and Sorghum vulgare (sorghum). Luteoforol is found in cereals and cereal products, fats and oils, and corn.
Luteoforol is found in cereals and cereal products. Luteoforol is a constituent of Zea mays (sweet corn) and Sorghum vulgare (sorghum).

同义名列表

5 个代谢物同义名

2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4,5,7-triol, 9ci; 2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4,5,7-triol; 3-Deoxyleucocyanidin; Luteoforol; Luteoforol



数据库引用编号

19 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(1)

代谢反应

83 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(81)

COVID-19 Disease Map(0)

PathBank(1)

PharmGKB(0)

26 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。

亚细胞结构定位 关联基因列表
Cytoplasm 6 ALB, FOXO1, GYS2, IRS1, PPARG, SLC2A2
Nucleus 5 ALB, FOXO1, IRS1, PPARA, PPARG
cytosol 5 ALB, FOXO1, GYS2, IRS1, PPARG
centrosome 1 ALB
nucleoplasm 4 FOXO1, IRS1, PPARA, PPARG
RNA polymerase II transcription regulator complex 1 PPARG
Cell membrane 1 SLC2A2
Multi-pass membrane protein 2 SLC2A2, SLC5A1
cell cortex 1 GYS2
Golgi apparatus 2 ALB, SI
Golgi membrane 1 INS
plasma membrane 4 IRS1, SI, SLC2A2, SLC5A1
Membrane 2 SI, SLC2A2
apical plasma membrane 3 SI, SLC2A2, SLC5A1
brush border 2 SI, SLC2A2
caveola 1 IRS1
extracellular exosome 3 ALB, SI, SLC5A1
endoplasmic reticulum 1 ALB
extracellular space 2 ALB, INS
perinuclear region of cytoplasm 2 PPARG, SLC5A1
mitochondrion 2 FOXO1, PCK2
protein-containing complex 1 ALB
intracellular membrane-bounded organelle 2 IRS1, PPARG
Secreted 2 ALB, INS
extracellular region 2 ALB, INS
mitochondrial matrix 1 PCK2
anchoring junction 1 ALB
Early endosome 1 SLC5A1
cell-cell junction 1 SLC2A2
Apical cell membrane 1 SLC5A1
intracellular vesicle 1 SLC5A1
receptor complex 1 PPARG
ciliary basal body 1 ALB
chromatin 3 FOXO1, PPARA, PPARG
cytoskeleton 1 GYS2
centriole 1 ALB
brush border membrane 1 SLC5A1
spindle pole 1 ALB
blood microparticle 1 ALB
endosome lumen 1 INS
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 ALB, INS
cortical actin cytoskeleton 1 GYS2
platelet alpha granule lumen 1 ALB
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
insulin receptor complex 1 IRS1
intracellular organelle 1 SLC5A1
ciliary transition fiber 1 ALB


文献列表

  • Mandeep Sharma, Chenglin Chai, Kengo Morohashi, Erich Grotewold, Maurice E Snook, Surinder Chopra. Expression of flavonoid 3'-hydroxylase is controlled by P1, the regulator of 3-deoxyflavonoid biosynthesis in maize. BMC plant biology. 2012 Nov; 12(?):196. doi: 10.1186/1471-2229-12-196. [PMID: 23113982]
  • Houhua Li, Jian Qiu, Fudong Chen, Xiaofen Lv, Chunxiang Fu, Dexiu Zhao, Xuejun Hua, Qiao Zhao. Molecular characterization and expression analysis of dihydroflavonol 4-reductase (DFR) gene in Saussurea medusa. Molecular biology reports. 2012 Mar; 39(3):2991-9. doi: 10.1007/s11033-011-1061-2. [PMID: 21701830]
  • Henryk Flachowsky, Heidi Halbwirth, Dieter Treutter, Klaus Richter, Magda-Viola Hanke, Iris Szankowski, Christian Gosch, Karl Stich, Thilo C Fischer. Silencing of flavanone-3-hydroxylase in apple (Malus × domestica Borkh.) leads to accumulation of flavanones, but not to reduced fire blight susceptibility. Plant physiology and biochemistry : PPB. 2012 Feb; 51(?):18-25. doi: 10.1016/j.plaphy.2011.10.004. [PMID: 22153235]
  • Daniela Fritz, Caroline Rita Venturi, Simone Cargnin, Jan Schripsema, Paulo Michel Roehe, Jarbas Alves Montanha, Gilsane Lino von Poser. Herpes virus inhibitory substances from Hypericum connatum Lam., a plant used in southern Brazil to treat oral lesions. Journal of ethnopharmacology. 2007 Sep; 113(3):517-20. doi: 10.1016/j.jep.2007.07.013. [PMID: 17719731]
  • N Ramesh, M B Viswanathan, A Saraswathy, P Brindha, K Balakrishna, P Lakshmanaperumalsamy, A Patra. Antibacterial activity of luteoforol from Bridelia crenulata. Fitoterapia. 2001 May; 72(4):409-11. doi: 10.1016/s0367-326x(00)00317-8. [PMID: 11395265]