5,6,7-Trimethoxycoumarin (BioDeep_00000002790)

 

Secondary id: BioDeep_00000861043

natural product PANOMIX_OTCML-2023 PANOMIX_OTCML-2025


Metabolite Card


5,6,7-trimethoxychromen-2-one

  Formula: C12H12O5 (236.0685)
Chinese Names: 三甲氧基香豆素
  Spectrum Hits: Top Source Viridiplantae(otcml) 29.68%

Reviewed

Last reviewed on 2025-06-05.

Cite this Page

5,6,7-Trimethoxycoumarin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/5,6,7-trimethoxycoumarin (retrieved 2025-06-17) (BioDeep RN: BioDeep_00000002790). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Molecular Structure

SMILES: c1(c(cc2c(c1OC)ccc(=O)o2)OC)OC
InChI: InChI=1S/C12H12O5/c1-14-9-6-8-7(4-5-10(13)17-8)11(15-2)12(9)16-3/h4-6H,1-3H3


Description

A member of the class of coumarins that is coumarin substituted by methoxy groups at positions 5, 6 and 7.

Synonyms

12 synonym names

5,6,7-Trimethoxycoumarin; 5,6,7-Trimethoxycoumarin; 2H-1-Benzopyran-2-one, 5,6,7-trimethoxy-; 5,6,7-trimethoxy-2H-1-benzopyran-2-one; 5,6,7-trimethoxy-2H-chromen-2-one; 5,6,7-trimethoxychromen-2-one; AC1L3XOT; DYC5EDM6W7; fraxinol methyl ether; UMCKALIN METHYL ETHER; UMCKALIN MONOMETHYL ETHER; UNII-DYC5EDM6W7



Cross Reference

35 cross reference id

Classification Terms

Related Pathways

Reactome(0)

BioCyc(0)

PlantCyc(0)

Biological Process

0 related biological process reactions.

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

29 organism taxonomy source information

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。



Literature Reference

  • InWha Park, Hee Sun Byun, Gang Min Hur, MinKyun Na. Tulipiferamide A, an Alkamide from Liriodendron tulipifera, Exhibits an Anti-Inflammatory Effect via Targeting IKKβ Phosphorylation. Journal of natural products. 2021 05; 84(5):1598-1606. doi: 10.1021/acs.jnatprod.1c00146. [PMID: 33939429]
  • Sung-Jin Lee, Hye Min Kim, Jeong Min Lee, Hee Seung Park, Sanghyun Lee. Artemisterol, a new steryl ester from the whole plant of Artemisia apiacea. Journal of Asian natural products research. 2008 Mar; 10(3-4):313-6. doi: 10.1080/10286020701782486. [PMID: 18348053]
  • M Asif Saeed, A W Sabir. Irritant and cytotoxic coumarins from Angelica glauca Edgew roots. Journal of Asian natural products research. 2008 Jan; 10(1-2):49-58. doi: 10.1080/10286020701273759. [PMID: 18058380]
  • Sanghyun Lee, Kyoung Soon Kim, Sang Hee Shim, You Mie Park, Bak-Kwang Kim. Constituents from the non-polar fraction of Artemisia apiacea. Archives of pharmacal research. 2003 Nov; 26(11):902-5. doi: 10.1007/bf02980197. [PMID: 14661854]
  • P Satyanarayana, K A Kumar, S K Singh, G N Rao. A new phorbol diester from Aleurites moluccana. Fitoterapia. 2001 Mar; 72(3):304-6. doi: 10.1016/s0367-326x(00)00314-2. [PMID: 11295313]