Afrormosin (BioDeep_00000018757)

Main id: BioDeep_00000016680

 

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


Afrormosin

化学式: C17H14O5 (298.0841194)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O
InChI: InChI=1S/C17H14O5/c1-20-11-5-3-10(4-6-11)13-9-22-15-8-14(18)16(21-2)7-12(15)17(13)19/h3-9,18H,1-2H3

描述信息

同义名列表

2 个代谢物同义名

Afrormosin; Afrormosin



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(1)

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)

155 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

  • Quentin Favre-Godal, Stephane Dorsaz, Emerson F Queiroz, Laurence Marcourt, Samad N Ebrahimi, Pierre-Marie Allard, Francine Voinesco, Matthias Hamburger, Mahabir P Gupta, Katia Gindro, Dominique Sanglard, Jean-Luc Wolfender. Anti-Candida Cassane-Type Diterpenoids from the Root Bark of Swartzia simplex. Journal of natural products. 2015 Dec; 78(12):2994-3004. doi: 10.1021/acs.jnatprod.5b00744. [PMID: 26654828]
  • Olekile Tibe, Lucy P Meagher, Karl Fraser, David R K Harding. Condensed tannins and flavonoids from the forage legume sulla (Hedysarum coronarium). Journal of agricultural and food chemistry. 2011 Sep; 59(17):9402-9. doi: 10.1021/jf2014759. [PMID: 21780793]
  • Sajida Abdureyim, Nurmuhammat Amat, Anwar Umar, Halmurat Upur, Benedicte Berke, Nicholas Moore. Anti-inflammatory, immunomodulatory, and heme oxygenase-1 inhibitory activities of ravan napas, a formulation of uighur traditional medicine, in a rat model of allergic asthma. Evidence-based complementary and alternative medicine : eCAM. 2011; 2011(?):. doi: 10.1155/2011/725926. [PMID: 20953388]
  • Pilar Puebla, Yoko Oshima-Franco, Luiz M Franco, Marcio G Dos Santos, Renata V da Silva, Leandro Rubem-Mauro, Arturo San Feliciano. Chemical constituents of the bark of Dipteryx alata vogel, an active species against Bothrops jararacussu venom. Molecules (Basel, Switzerland). 2010 Nov; 15(11):8193-204. doi: 10.3390/molecules15118193. [PMID: 21076386]
  • Cheng Xiang, Jun Cheng, Hong Liang, Yu-Ying Zhao, Jie Feng. [Isoflavones from Millettia nitida var. hirsutissima]. Yao xue xue bao = Acta pharmaceutica Sinica. 2009 Feb; 44(2):158-61. doi: ". [PMID: 19408686]
  • Jie Feng, Cheng Xiang, Hong Liang, Yu-Ying Zhao. [Chemical constituents of isoflavones from vine stems of Millettia nitita var. hirsutissima]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2007 Feb; 32(4):321-2. doi: ". [PMID: 17455468]
  • Junsong Wang, Xianwen Yang, Yingtong Di, Yuehu Wang, Yuemao Shen, Xiaojiang Hao. Isoflavone diglycosides from Glycosmis pentaphylla. Journal of natural products. 2006 May; 69(5):778-82. doi: 10.1021/np060001q. [PMID: 16724840]
  • Maria Halabalaki, Xanthippi Alexi, Nektarios Aligiannis, George Lambrinidis, Harris Pratsinis, Ida Florentin, Sofia Mitakou, Emmanuel Mikros, Alexios-Leandros Skaltsounis, Michael N Alexis. Estrogenic activity of isoflavonoids from Onobrychis ebenoides. Planta medica. 2006 May; 72(6):488-93. doi: 10.1055/s-2005-916261. [PMID: 16773531]
  • Wei Wang, Hong Liang, Bin Wang, Guang-zhong Tu, Hu-biao Chen, Yu-ying Zhao. [A new natural product from the roots of Hedysarum multijugum]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 2005 Oct; 37(5):532-5. doi: . [PMID: 16224530]
  • A S Saratikov, V S Chuchalin, A V Rat'kin, E V Rat'kin, S A Fedoreev, V P Bulgakov. [Hepatoprotector properties of polyphenolic complexes from wood and cell culture of Maackia amurensis]. Eksperimental'naia i klinicheskaia farmakologiia. 2005 Mar; 68(2):51-4. doi: . [PMID: 15934369]
  • L Li, H K Wang, J J Chang, A T McPhail, D R McPhail, H Terada, T Konoshima, M Kokumai, M Kozuka, J R Estes. Antitumor agents, 138. Rotenoids and isoflavones as cytotoxic constitutents from Amorpha fruticosa. Journal of natural products. 1993 May; 56(5):690-8. doi: 10.1021/np50095a005. [PMID: 8326318]
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