(-)-DCA (BioDeep_00000396478)

 

Secondary id: BioDeep_00000266995

PANOMIX_OTCML-2023


代谢物信息卡片


4-{(2R,3S)-3-(hydroxymethyl)-5-[(1E)-3-hydroxyprop-1-en-1-yl]-7-methoxy-2,3-dihydro-1-benzofuran-2-yl}-2-methoxyphenol

化学式: C20H22O6 (358.1416312)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(blood) 14.29%

分子结构信息

SMILES: COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO
InChI: InChI=1S/C20H22O6/c1-24-17-10-13(5-6-16(17)23)19-15(11-22)14-8-12(4-3-7-21)9-18(25-2)20(14)26-19/h3-6,8-10,15,19,21-23H,7,11H2,1-2H3/b4-3+/t15-,19+/m1/s1

描述信息

(-)-dehydrodiconiferyl alcohol is a dehydrodiconiferyl alcohol that has (2R,3S)-configuration. It is a natural product isolated from several plant species including Aglaia foveolata, Viburnum erosum and Rosa multiflora. It has a role as a plant metabolite. It is an enantiomer of a (+)-dehydrodiconiferyl alcohol.
(-)-Dehydrodiconiferyl Alcohol is a natural product found in Campylotropis hirtella, Kadsura coccinea, and other organisms with data available.
A dehydrodiconiferyl alcohol that has (2R,3S)-configuration. It is a natural product isolated from several plant species including Aglaia foveolata, Viburnum erosum and Rosa multiflora.

同义名列表

11 个代谢物同义名

4-{(2R,3S)-3-(hydroxymethyl)-5-[(1E)-3-hydroxyprop-1-en-1-yl]-7-methoxy-2,3-dihydro-1-benzofuran-2-yl}-2-methoxyphenol; (2R)-5-[(E)-3-Hydroxy-1-propenyl]-2,3-dihydro-2beta-(4-hydroxy-3-methoxyphenyl)-7-methoxybenzofuran-3alpha-methanol; 4-[(2R,3S)-3-(hydroxymethyl)-5-[(E)-3-hydroxyprop-1-enyl]-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenol; (2R,3S)-2,3-Dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-[(1E)-3-hydroxy-1-propen-1-yl]-7-methoxy-3-benzofuranmethanol; 7-Methoxy-5-[(E)-3-hydroxy-1-propenyl]-2beta-(3-methoxy-4-hydroxyphenyl)-2,3-dihydrobenzofuran-3alpha-methanol; (-)-(2R,3S)-dehydrodiconiferyl alcohol; (7R,8S)-Dehydrodiconiferyl alcohol; (2R,3S)-dehydrodiconiferyl alcohol; (-)-Dehydrodiconiferyl Alcohol; 5-O-Methylhierochin D; (-)-DCA



数据库引用编号

6 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(0)

代谢反应

1 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

9 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

  • Li-Li Lou, Guo-Dong Yao, Jie Wang, Wen-Yu Zhao, Xiao-Bo Wang, Xiao-Xiao Huang, Shao-Jiang Song. Enantiomeric neolignans from Picrasma quassioides exhibit distinctive cytotoxicity on hepatic carcinoma cells through ROS generation and apoptosis induction. Bioorganic & medicinal chemistry letters. 2018 05; 28(8):1263-1268. doi: 10.1016/j.bmcl.2018.03.043. [PMID: 29567344]
  • Eun Ju Jeong, Jung Hee Cho, Sang Hyun Sung, Sun Yeou Kim, Young Choong Kim. Inhibition of nitric oxide production in lipopolysaccharide-stimulated RAW264.7 macrophage cells by lignans isolated from Euonymus alatus leaves and twigs. Bioorganic & medicinal chemistry letters. 2011 Apr; 21(8):2283-6. doi: 10.1016/j.bmcl.2011.02.102. [PMID: 21435874]
  • Francesca Cutillo, Brigida D'Abrosca, Marina DellaGreca, Antonio Fiorentino, Armando Zarrelli. Lignans and neolignans from Brassica fruticulosa: effects on seed germination and plant growth. Journal of agricultural and food chemistry. 2003 Oct; 51(21):6165-72. doi: 10.1021/jf034644c. [PMID: 14518939]