Herniarin (BioDeep_00000000258)

Main id: BioDeep_00000000248

Secondary id: BioDeep_00000406716, BioDeep_00000863311

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


7-Methoxycoumarin, suitable for fluorescence, >=98.0\\% (TLC)

化学式: C10H8O3 (176.0473418)
中文名称: 7-甲氧基香豆素, 甲氧基香豆素, 脱肠草内酯, 脱肠草素, 7-甲氧基香豆素
谱图信息: 最多检出来源 Macaca mulatta(otcml) 1.38%

分子结构信息

SMILES: c1c(cc2c(c1)ccc(=O)o2)OC
InChI: InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3

描述信息

Herniarin, also known as 7-methoxycoumarin or ayapanin, belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). Herniarin is a sweet, balsamic, and tonka tasting compound. Herniarin has been detected, but not quantified, in several different foods, such as barley, tarragons, roman camomiles, fruits, and wild celeries. This could make herniarin a potential biomarker for the consumption of these foods.
Herniarin is a member of the class of coumarins that is coumarin substituted by a methoxy group at position 7. It has a role as a fluorochrome.
7-Methoxycoumarin is a natural product found in Haplopappus multifolius, Herniaria hirsuta, and other organisms with data available.
See also: Chamomile (part of); Glycyrrhiza Glabra (part of).
Present in Prunus mahaleb (mahaleb cherry). Herniarin is found in many foods, some of which are caraway, wild celery, barley, and fruits.
A member of the class of coumarins that is coumarin substituted by a methoxy group at position 7.
Herniarin is a natural coumarin occurs in some flowering plants, with antitumor effect.
Herniarin is a natural coumarin occurs in some flowering plants, with antitumor effect.

同义名列表

50 个代谢物同义名

7-Methoxycoumarin, suitable for fluorescence, >=98.0\\% (TLC); Herniarin, primary pharmaceutical reference standard; 7-METHOXYCOUMARIN (CONSTITUENT OF CHAMOMILE) [DSC]; 7-Methoxycoumarin 100 microg/mL in Acetonitrile; 7-METHOXYCOUMARIN (CONSTITUENT OF CHAMOMILE); 5-18-01-00387 (Beilstein Handbook Reference); 7-Methoxycoumarin;Methyl umbelliferyl ether; 7-Methyl ether derivative of Umbelliferone; 7-Methoxycoumarin, analytical standard; 7-Methoxy-2H-1-benzopyran-2-one, 9CI; 2H-1-BENZOPYRAN-2-ONE, 7-METHOXY-; 7-Methoxy-2H-1-benzopyran-2-one; 7-(methyloxy)-2H-chromen-2-one; 7-methoxy-1-benzopyran-2-one; 7-Methoxy-2H-chromen-2-one #; Umbelliferone, methyl ether; Coumarin, 7-methoxy- (8CI); 7-Methoxy-2H-chromen-2-one; Umbelliferone methyl ether; Methyl umbelliferyl ether; 7-Methoxycoumarin, >=98\\%; 7-methoxy-chromen-2-one; 7-methoxychromen-2-one; Coumarin, 7-methoxy-; METHOXYCOURMARIN, 7-; METHOXYCOUMARIN, 7-; Methylumbelliferone; 7-METHOXYCOURMARIN; 7-Methoxy Coumarin; 7-methoxy-coumarin; 7-Methoxycoumarin; Spectrum4_001558; Spectrum3_000263; Spectrum2_000398; Spectrum5_000156; UNII-DGK72G008A; Herniarin (6CI); DivK1c_006418; Herniarin,(S); MEGxp0_000150; ACon1_002037; KBio1_001362; KBio2_003440; KBio2_006008; KBio3_001206; KBio2_000872; Herniarine; DGK72G008A; herniarin; Ayapanin



数据库引用编号

22 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

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(1)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

127 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

  • Arman Mokaram Doust Delkhah, Ehsan Karimi, Shirin Farivar. Herniarin-loaded solid lipid nanoparticles: promising molecular mechanism and therapeutic potential against pancreatic cancer line. Molecular biology reports. 2023 Jun; ?(?):. doi: 10.1007/s11033-023-08560-9. [PMID: 37326747]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Sandra Liliana Porras-Dávila, Alejandro Zamilpa, Enrique Jiménez-Ferrer, Antonio Jiménez-Aparicio, Mayra Alejandra Santillán-Urquiza, Fernanda Díaz-Patricio, Maribel Herrera-Ruiz. Anti-inflammatory and Neuroprotective effects of standardized fractions in herniarin and daphnoretin from Distictis buccinatoria. Chemistry & biodiversity. 2023 Mar; ?(?):e202200969. doi: 10.1002/cbdv.202200969. [PMID: 36973180]
  • Elham Al Fares, Tamar Sanikidze, Sophio Kalmakhelidze, David Topuria, Luigi Mansi, Sean Kitson, Mikaeil Molazadeh. The Alleviating Effect of Herniarin Against Ionizing Radiation-Induced Genotoxicity and Cytotoxicity in Human Peripheral Blood Lymphocytes. Current radiopharmaceuticals. 2022; 15(2):141-147. doi: 10.2174/1874471014666211012104808. [PMID: 34636317]
  • Samira Asgharzade, Mohammad Bagher Khorrami, Fatemeh Forouzanfar. Neuroprotective effect of herniarin following transient focal cerebral ischemia in rats. Metabolic brain disease. 2021 12; 36(8):2505-2510. doi: 10.1007/s11011-021-00841-1. [PMID: 34519909]
  • Jingxuan Ke, Jinxi Cheng, Qingying Luo, Hejun Wu, Guanghui Shen, Zhiqing Zhang. Identification of two bitter components in Zanthoxylum bungeanum Maxim. and exploration of their bitter taste mechanism through receptor hTAS2R14. Food chemistry. 2021 Feb; 338(?):127816. doi: 10.1016/j.foodchem.2020.127816. [PMID: 32818866]
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