mearnsetin (BioDeep_00000359526)

   

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


mearnsetin

化学式: C16H12O8 (332.0532152)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=CC2OC(C3C=C(O)C(OC)=C(O)C=3)=C(O)C(=O)C=2C(O)=C1
InChI: InChI=1S/C16H12O8/c1-23-16-9(19)2-6(3-10(16)20)15-14(22)13(21)12-8(18)4-7(17)5-11(12)24-15/h2-5,17-20,22H,1H3

描述信息

同义名列表

1 个代谢物同义名

mearnsetin



数据库引用编号

8 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)

30 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

  • Lalith Jayasinghe, Nilupa R Amarasinghe, B G Suranga Arundathie, G Kalinga Rupasinghe, N H Ayona N Jayatilake, Yoshinori Fujimoto. Antioxidant flavonol glycosides from Elaeocarpus serratus and Filicium decipiens. Natural product research. 2012; 26(8):717-21. doi: 10.1080/14786419.2010.551514. [PMID: 21923561]
  • Sónia A O Santos, Carmen S R Freire, M Rosário M Domingues, Armando J D Silvestre, Carlos Pascoal Neto. Characterization of phenolic components in polar extracts of Eucalyptus globulus Labill. bark by high-performance liquid chromatography-mass spectrometry. Journal of agricultural and food chemistry. 2011 Sep; 59(17):9386-93. doi: 10.1021/jf201801q. [PMID: 21761864]
  • Elizabeth A Mazzio, Fran Close, Karam F A Soliman. The biochemical and cellular basis for nutraceutical strategies to attenuate neurodegeneration in Parkinson's disease. International journal of molecular sciences. 2011 Jan; 12(1):506-69. doi: 10.3390/ijms12010506. [PMID: 21340000]
  • Fawkeya A Abbas, Shaza M Al-Massarany, Shabana Khan, Tawfeq A Al-Howiriny, Jaber S Mossa, Ehab A Abourashed. Phytochemical and biological studies on Saudi Commiphora opobalsamum L. Natural product research. 2007 May; 21(5):383-91. doi: 10.1080/14786410600942025. [PMID: 17487607]
  • Guo-xun Yang, Jian-bin Qi, Ke-jun Cheng, Chang-qi Hu. [Anti-HIV chemical constituents of aerial parts of Caragana rosea]. Yao xue xue bao = Acta pharmaceutica Sinica. 2007 Feb; 42(2):179-82. doi: . [PMID: 17518047]
  • Hiroyuki Nakagawa, Yoshihisa Takaishi, Yoshinori Fujimoto, Carmenza Duque, Cristina Garzon, Mitsunobu Sato, Masato Okamoto, Tetsuya Oshikawa, Sharif Uddin Ahmed. Chemical constituents from the Colombian medicinal plant Maytenus laevis. Journal of natural products. 2004 Nov; 67(11):1919-24. doi: 10.1021/np040006s. [PMID: 15568791]
  • Erdal Bedir, Irem I Tatli, Riaz A Khan, Jianping Zhao, Satoshi Takamatsu, Larry A Walker, Peter Goldman, Ikhlas A Khan. Biologically active secondary metabolites from Ginkgo biloba. Journal of agricultural and food chemistry. 2002 May; 50(11):3150-5. doi: 10.1021/jf011682s. [PMID: 12009978]
  • I I Mahmoud, M S Marzouk, F A Moharram, M R El-Gindi, A M Hassan. Acylated flavonol glycosides from Eugenia jambolana leaves. Phytochemistry. 2001 Dec; 58(8):1239-44. doi: 10.1016/s0031-9422(01)00365-x. [PMID: 11738415]