teucrin A (BioDeep_00000323396)

   

natural product


代谢物信息卡片


NCGC00385790-01_C19H20O6_(3S,5S,5aS,7S,8S,8aR)-5-(3-Furyl)-8-hydroxy-7-methyl-3,4,5,5,5a,7,8,8a-octahydrospiro[furan-3,6-naphtho[1,8-bc]furan]-2,2(4H)-dione

化学式: C19H20O6 (344.125982)
中文名称: 石蚕苷A
谱图信息: 最多检出来源 Viridiplantae(plant) 12.7%

分子结构信息

SMILES: CC1C(C2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2)O
InChI: InChI=1S/C19H20O6/c1-9-15(20)16-14-11(17(21)25-16)3-2-4-12(14)19(9)7-13(24-18(19)22)10-5-6-23-8-10/h5-6,8-9,12-13,15-16,20H,2-4,7H2,1H3/t9-,12+,13+,15+,16-,19-/m1/s1



数据库引用编号

7 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)

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

  • ". Standard Method Performance Requirements (SMPRs®) 2018.008: Determination of Selected Compounds from Teucrium spp. in Skullcap Materials in Commerce. Journal of AOAC International. 2019 Jan; 102(1):330-334. doi: 10.1093/jaoac/102.1.330. [PMID: 30594276]
  • Alexandra Druckova, Raymond L Mernaugh, Amy-Joan L Ham, Lawrence J Marnett. Identification of the protein targets of the reactive metabolite of teucrin A in vivo in the rat. Chemical research in toxicology. 2007 Oct; 20(10):1393-408. doi: 10.1021/tx7001405. [PMID: 17892266]
  • E Bosisio, F Giavarini, M Dell'Agli, G Galli, C L Galli. Analysis by high-performance liquid chromatography of teucrin A in beverages flavoured with an extract of Teucrium chamaedrys L. Food additives and contaminants. 2004 May; 21(5):407-14. doi: 10.1080/02652030410001670157. [PMID: 15204541]
  • V De Berardinis, C Moulis, M Maurice, P Beaune, D Pessayre, D Pompon, J Loeper. Human microsomal epoxide hydrolase is the target of germander-induced autoantibodies on the surface of human hepatocytes. Molecular pharmacology. 2000 Sep; 58(3):542-51. doi: 10.1124/mol.58.3.542. [PMID: 10953047]
  • M Lekehal, D Pessayre, J M Lereau, C Moulis, I Fouraste, D Fau. Hepatotoxicity of the herbal medicine germander: metabolic activation of its furano diterpenoids by cytochrome P450 3A Depletes cytoskeleton-associated protein thiols and forms plasma membrane blebs in rat hepatocytes. Hepatology (Baltimore, Md.). 1996 Jul; 24(1):212-8. doi: 10.1002/hep.510240134. [PMID: 8707265]
  • S A Kouzi, R J McMurtry, S D Nelson. Hepatotoxicity of germander (Teucrium chamaedrys L.) and one of its constituent neoclerodane diterpenes teucrin A in the mouse. Chemical research in toxicology. 1994 Nov; 7(6):850-6. doi: 10.1021/tx00042a020. [PMID: 7696542]