Balanophonin (BioDeep_00000343059)

   

PANOMIX_OTCML-2023


代谢物信息卡片


(2E)-3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl] acrylaldehyde

化学式: C20H20O6 (356.125982)
中文名称: 右旋蛇菰宁, 蛇菰宁
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 46.15%

分子结构信息

SMILES: COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O
InChI: InChI=1S/C20H20O6/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/h3-10,15,19,22-23H,11H2,1-2H3/b4-3+/t15-,19+/m0/s1

描述信息

(+)-Balanophonin is a natural product found in Balanophora japonica, Catunaregam spinosa, and other organisms with data available.
Balanophonin is a natural product found in Lonicera insularis, Carya cathayensis, and other organisms with data available.

同义名列表

16 个代谢物同义名

(2E)-3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl] acrylaldehyde; 2-Propenal, 3-[2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-5-benzofuranyl]-, [2,3,5(E)]-; (E)-3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal; (E)-3-((2S,3R)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)acrylaldehyde; ( inverted exclamation markA)-Balanophonin; (+)-dehydrodiconiferyl aldehyde; (+/-)-balanophonin; (-)-balanophonin; (+)-Balanophonin; ()-Balanophonin; Balanophonin; (+)-DCA-L; (2E)-3-[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl] acrylaldehyde; (E)-3-((2R,3S)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)acrylaldehyde; (-)-dehydrodiconiferyl aldehyde; (-)-DCA-L



数据库引用编号

12 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)

0 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

  • Rita Könye, Gergő Tóth, Anna Sólyomváry, Zsolt Mervai, Moritz Zürn, Kornélia Baghy, Ilona Kovalszky, Péter Horváth, Ibolya Molnár-Perl, Béla Noszál, Szabolcs Béni, Imre Boldizsár. Chemodiversity of Cirsium fruits: Antiproliferative lignans, neolignans and sesquineolignans as chemotaxonomic markers. Fitoterapia. 2018 Jun; 127(?):413-419. doi: 10.1016/j.fitote.2018.04.007. [PMID: 29653155]
  • 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]
  • Yue-ping Jiang, Yu-feng Liu, Qing-lan Guo, Cheng-bo Xu, Sheng Lin, Cheng-gen Zhu, Yong-chun Yang, Jian-gong Shi. [Lignanoids from an aqueous extract of the roots of Codonopsis pilosula]. Yao xue xue bao = Acta pharmaceutica Sinica. 2016 04; 51(4):616-25. doi: . [PMID: 29860746]
  • 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]
  • ". [Chemical Constituents from Serissa japonica]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Jan; 39(1):94-7. doi: ". [PMID: 30080007]
  • Gui-hui Wu, Yan Chen, Li-hua Zheng, Tao Huang, Xiao-jiang Hao, Jian-xin Zhang. [Chemical Constituents of Eucommia ulmoides in Guizhou Province]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 May; 38(5):980-4. doi: . [PMID: 26767291]
  • I Boldizsár, M Kraszni, F Tóth, G Tóth, A Sólyomváry, B Noszál, Gy Záray, I Molnár-Perl. The role of harmonized, gas and liquid chromatography mass spectrometry in the discovery of the neolignan balanophonin in the fruit wall of Cirsium vulgare. Journal of chromatography. A. 2012 Nov; 1264(?):143-7. doi: 10.1016/j.chroma.2012.09.073. [PMID: 23068765]
  • Wei Wu, Xiu-Li Bi, Jia-Qing Cao, Kai-Qing Zhang, Yu-Qing Zhao. New antitumor compounds from Carya cathayensis. Bioorganic & medicinal chemistry letters. 2012 Mar; 22(5):1895-8. doi: 10.1016/j.bmcl.2012.01.062. [PMID: 22330636]
  • Joo Hee Kwon, Jee Hun Kim, Sun Eun Choi, Kwan Hee Park, Min Won Lee. Inhibitory effects of phenolic compounds from needles of Pinus densiflora on nitric oxide and PGE2 production. Archives of pharmacal research. 2010 Dec; 33(12):2011-6. doi: 10.1007/s12272-010-1217-y. [PMID: 21191767]
  • Souichi Nakashima, Hisashi Matsuda, Yoshimi Oda, Seikou Nakamura, Fengming Xu, Masayuki Yoshikawa. Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells. Bioorganic & medicinal chemistry. 2010 Mar; 18(6):2337-2345. doi: 10.1016/j.bmc.2010.01.046. [PMID: 20189399]