Cyclo(pro-val) (BioDeep_00000169838)

 

Secondary id: BioDeep_00000403027, BioDeep_00000403705, BioDeep_00001876006

human metabolite PANOMIX_OTCML-2023 blood metabolite Cytotoxicity natural product


代谢物信息卡片


(3S,8aS)-1-hydroxy-3-(propan-2-yl)-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

化学式: C10H16N2O2 (196.1211716)
中文名称: 环(L-脯-L-缬)二肽, 环(脯氨酸-缬氨酸)二肽
谱图信息: 最多检出来源 Viridiplantae(plant) 0.11%

Reviewed

Last reviewed on 2024-09-13.

Cite this Page

Cyclo(pro-val). BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/cyclo(pro-val) (retrieved 2024-11-24) (BioDeep RN: BioDeep_00000169838). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: CC(C)C1C(=O)N2CCCC2C(=O)N1
InChI: InChI=1S/C10H16N2O2/c1-6(2)8-10(14)12-5-3-4-7(12)9(13)11-8/h6-8H,3-5H2,1-2H3,(H,11,13)/t7-,8-/m0/s1

描述信息

Cyclo(L-Pro-L-Val) is a 2,5-diketopiperazine, with toxic activity against phytopathogenic microorganisms (such as R. fascians LMG 3605). Cyclo(L-Pro-L-Val) shows toxicity similar to Chloramphenicol (HY-B0239) with comparable concentration. Cyclo(L-Pro-L-Val) can also inhibit gram-positive phytopathogenic bacterium. Cyclo(L-Pro-L-Val) has potential development as biopesticide[1].
Cyclo(L-Pro-L-Val) is a 2,5-diketopiperazine, with toxic activity against phytopathogenic microorganisms (such as R. fascians LMG 3605). Cyclo(L-Pro-L-Val) shows toxicity similar to Chloramphenicol (HY-B0239) with comparable concentration. Cyclo(L-Pro-L-Val) can also inhibit gram-positive phytopathogenic bacterium. Cyclo(L-Pro-L-Val) has potential development as biopesticide[1].
Cyclo(Pro-Val) can be isolated from Pseudomonas fluorescens GcM5-1A and has cytotoxicity[1].

同义名列表

6 个代谢物同义名

(3S,8aS)-1-hydroxy-3-(propan-2-yl)-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one; (3S,8aS)-1-hydroxy-3-isopropyl-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one; Cyclo(L-prolyl-L-valyl); Cyclo(prolyl-valyl); Cyclo(L-pro-L-val); Cyclo(pro-val)



数据库引用编号

11 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)

85 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

  • Dahae Lee, Seoung Rak Lee, Ki Sung Kang, Ki Hyun Kim. Bioactive Phytochemicals from Mulberry: Potential Anti-Inflammatory Effects in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages. International journal of molecular sciences. 2021 Jul; 22(15):. doi: 10.3390/ijms22158120. [PMID: 34360887]
  • Omar González, Randy Ortíz-Castro, César Díaz-Pérez, Alma L Díaz-Pérez, Viridiana Magaña-Dueñas, José López-Bucio, Jesús Campos-García. Non-ribosomal Peptide Synthases from Pseudomonas aeruginosa Play a Role in Cyclodipeptide Biosynthesis, Quorum-Sensing Regulation, and Root Development in a Plant Host. Microbial ecology. 2017 04; 73(3):616-629. doi: 10.1007/s00248-016-0896-4. [PMID: 27900439]
  • Lei Jiang, Huaixiu Wen, Yun Shao, Ruitao Yu, Zenggen Liu, Shuo Wang, Qilan Wang, Xiaohui Zhao, Peng Zhang, Yanduo Tao, Lijuan Mei. Novel Diketopiperazine Dihydroorotate Dehydrogenase Inhibitors Purified from Traditional Tibetan Animal Medicine Osteon Myospalacem Baileyi. Chemical biology & drug design. 2015 Oct; 86(4):626-36. doi: 10.1111/cbdd.12530. [PMID: 25626527]
  • Hee Sook Chung, Soo-Yeun Lee. Modification of ginseng flavors by bitter compounds found in chocolate and coffee. Journal of food science. 2012 Jun; 77(6):S202-10. doi: 10.1111/j.1750-3841.2012.02716.x. [PMID: 22591221]