EVOXINE (BioDeep_00000003759)

   

natural product


Metabolite Card


2,3-Butanediol, 1-((4,8-dimethoxyfuro(2,3-b)quinolin-7-yl)oxy)-3-methyl-, (+)-

Formula: C18H21NO6 (347.1369)
Chinese Names: 尖叶云香碱
Spectrum Hits: Top Source Viridiplantae(plant) 14.36%

Molecular Structure

SMILES: c1c(c(c2c(c1)c(c1c(n2)occ1)OC)OC)OC[C@@H](C(C)(O)C)O
InChI: InChI=1S/C18H21NO6/c1-18(2,21)13(20)9-25-12-6-5-10-14(16(12)23-4)19-17-11(7-8-24-17)15(10)22-3/h5-8,13,20-21H,9H2,1-4H3/t13-/m0/s1

Description

Synonyms

28 synonym names

2,3-Butanediol, 1-((4,8-dimethoxyfuro(2,3-b)quinolin-7-yl)oxy)-3-methyl-, (+)-; 7-(2,3-Dihydroxy-3-methyl-butyl)oxy-8-methyldictamnine; EVOXINE; Evoxine; (+)-1-((4,8-Dimethoxyfuro(2,3-b)quinolin-7-yl)oxy)-3-methyl-2,3-butanediol; 1-(4,8-dimethoxyfurano[2,3-b]quinolin-7-yloxy)-3-methylbutane-2,3-diol; 1-(4,8-dimethoxyfuro(2,3-b)quinolin-7-yl)oxy-3-methyl-butane-2,3-diol; 1-(4,8-dimethoxyfuro(2,3-b)quinolin-7-yl)oxy-3-methylbutane-2,3-diol; 1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methyl-butane-2,3-diol; 1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methylbutane-2,3-diol; 1-[(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy]-3-methyl-2,3-butanediol; 1-[(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy]-3-methylbutane-2,3-diol; 2,3-Butanediol, 1-[(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy]-3-methyl-, (+)-; DivK1c_006700; Evoxine (Haploperine); KBio1_001644; KBio2_002214; KBio2_004782; KBio2_007350; KBio3_001869; NCI60_042106; Prestwick0_000665; Prestwick1_000665; Prestwick2_000665; Spectrum2_001625; Spectrum3_000985; Spectrum4_001111; Spectrum5_001911



Cross Reference

31 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)

63 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

  • Nishikant Wase, Boqiang Tu, James W Allen, Paul N Black, Concetta C DiRusso. Identification and Metabolite Profiling of Chemical Activators of Lipid Accumulation in Green Algae. Plant physiology. 2017 Aug; 174(4):2146-2165. doi: 10.1104/pp.17.00433. [PMID: 28652262]
  • Joyce J Kiplimo, Md Shahidul Islam, Neil A Koorbanally. A novel flavonoid and furoquinoline alkaloids from Vepris glomerata and their antioxidant activity. Natural product communications. 2011 Dec; 6(12):1847-50. doi: . [PMID: 22312722]
  • Luis Enrique Cuca Suarez, Manuel Elkin Pattarroyo, Jose Manuel Lozano, Franco Delle Monache. Biological activity of secondary metabolites from Peltostigma guatemalense. Natural product research. 2009; 23(4):370-4. doi: 10.1080/14786410802228439. [PMID: 19296377]
  • Alain F Kamdem Waffo, Philip H Coombes, Neil R Crouch, Dulcie A Mulholland, Sawsan M M El Amin, Peter J Smith. Acridone and furoquinoline alkaloids from Teclea gerrardii (Rutaceae: Toddalioideae) of southern Africa. Phytochemistry. 2007 Mar; 68(5):663-7. doi: 10.1016/j.phytochem.2006.10.011. [PMID: 17174364]
  • J H Holmes, I Kanfer, H Zwarenstein. Effect of benzodiazepine derivatives on human blood cholinesterase in vitro. Research communications in chemical pathology and pharmacology. 1978 Aug; 21(2):367-70. doi: . [PMID: 29327]