(-)-Pinoresinol (BioDeep_00000000688)

   

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


4-[(3R,3aS,6R,6aS)-6-(3-methoxy-4-oxidanyl-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxy-phenol

化学式: C20H22O6 (358.1416312)
中文名称: (-)-松脂醇
谱图信息: 最多检出来源 Viridiplantae(plant) 19.29%

分子结构信息

SMILES: COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O
InChI: InChI=1S/C20H22O6/c1-23-17-7-11(3-5-15(17)21)19-13-9-26-20(14(13)10-25-19)12-4-6-16(22)18(8-12)24-2/h3-8,13-14,19-22H,9-10H2,1-2H3/t13-,14-,19+,20+/m1/s1

描述信息

(-)-pinoresinol is an enantiomer of pinoresinol having (-)-1R,3aS,4R,6aS-configuration. It has a role as a plant metabolite.
(-)-Pinoresinol is a natural product found in Dendrobium loddigesii, Forsythia suspensa, and other organisms with data available.
An enantiomer of pinoresinol having (-)-1R,3aS,4R,6aS-configuration.

同义名列表

7 个代谢物同义名

4-[(3R,3aS,6R,6aS)-6-(3-methoxy-4-oxidanyl-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxy-phenol; 4-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol; 4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3-methoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2-methoxyphenol; 4,4-(1R,3aS,4R,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diylbis(2-methoxyphenol); (7beta,7beta,8beta,8beta)-3,3-dimethoxy-7,9:7,9-diepoxylignane-4,4-diol; (-)-Pinoresinol; (?)-Pinoresinol



数据库引用编号

10 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(1)

代谢反应

114 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(2)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(112)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

154 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

  • Di Zhou, Hongyan Wei, Zhe Jiang, Xuezheng Li, Kun Jiao, Xiaoguang Jia, Yue Hou, Ning Li. Natural potential neuroinflammatory inhibitors from Alhagi sparsifolia Shap. Bioorganic & medicinal chemistry letters. 2017 02; 27(4):973-978. doi: 10.1016/j.bmcl.2016.12.075. [PMID: 28073678]
  • Won Se Suh, Lalita Subedi, Sun Yeou Kim, Sang Un Choi, Kang Ro Lee. Bioactive lignan constituents from the twigs of Sambucus williamsii. Bioorganic & medicinal chemistry letters. 2016 Apr; 26(8):1877-80. doi: 10.1016/j.bmcl.2016.03.023. [PMID: 26988298]
  • Kyeong Wan Woo, Won Se Suh, Lalita Subedi, Sun Yeou Kim, Aejung Kim, Kang Ro Lee. Bioactive lignan derivatives from the stems of Firmiana simplex. Bioorganic & medicinal chemistry letters. 2016 Feb; 26(3):730-733. doi: 10.1016/j.bmcl.2016.01.008. [PMID: 26774654]
  • Sooryun Lee, Inn-Hye Song, Jung-Ho Lee, Woo-Young Yang, Ki-Bong Oh, Jongheon Shin. Sortase A inhibitory metabolites from the roots of Pulsatilla koreana. Bioorganic & medicinal chemistry letters. 2014 Jan; 24(1):44-8. doi: 10.1016/j.bmcl.2013.12.006. [PMID: 24360605]
  • Nguyen X Nhiem, Phan V Kiem, Chau V Minh, Nanyoung Kim, Seonju Park, Hwa Young Lee, Eun Sil Kim, Young Ho Kim, Sohyun Kim, Young-Sang Koh, Seung Hyun Kim. Diarylheptanoids and flavonoids from viscum album inhibit LPS-stimulated production of pro-inflammatory cytokines in bone marrow-derived dendritic cells. Journal of natural products. 2013 Apr; 76(4):495-502. doi: 10.1021/np300490v. [PMID: 23484668]
  • Ji Sang Hwang, Seon A Lee, Seong Su Hong, Xiang Hua Han, Chul Lee, Dongho Lee, Chong-Kil Lee, Jin Tae Hong, Youngsoo Kim, Mi Kyeong Lee, Bang Yeon Hwang. Inhibitory constituents of Nardostachys chinensis on nitric oxide production in RAW 264.7 macrophages. Bioorganic & medicinal chemistry letters. 2012 Jan; 22(1):706-8. doi: 10.1016/j.bmcl.2011.10.043. [PMID: 22079762]
  • Suresh Awale, Feng Li, Hiroko Onozuka, Hiroyasu Esumi, Yasuhiro Tezuka, Shigetoshi Kadota. Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition. Bioorganic & medicinal chemistry. 2008 Jan; 16(1):181-9. doi: 10.1016/j.bmc.2007.10.004. [PMID: 17950610]
  • Y Mimaki, M Kuroda, T Asano, Y Sashida. Triterpene saponins and lignans from the roots of Pulsatilla chinensis and their cytotoxic activity against HL-60 cells. Journal of natural products. 1999 Sep; 62(9):1279-83. doi: 10.1021/np9901837. [PMID: 10514313]