Phenylpropiolic acid (BioDeep_00000027077)

Main id: BioDeep_00000405529

 

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds


代谢物信息卡片


Phenylacetylene monocarboxylic acid

化学式: C9H6O2 (146.0367776)
中文名称: 苯丙炔酸, 苯丙酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C(C=C1)C#CC(=O)O
InChI: InChI=1S/C9H6O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5H,(H,10,11)

描述信息

Phenylpropiolic acid is an acetylenic compound that is propynoic acid in which the acetylenic hydrogen is replaced by a phenyl group. It is an alpha,beta-unsaturated monocarboxylic acid, an acetylenic compound and a member of benzenes. It derives from a propynoic acid. Phenylpropiolic acid is one of a number of phenylpropanoid, natural products occurring in plants pathways involved in plant resistance providing building units of physical barriers against pathogen invasion, synthesizing an array of antibiotic compounds, and producing signals implicated in the mounting of plant resistance. (PMID 15199968). Phenylpropiolic acid is a cis-pyrrolidinone that has been tested as an inhibitors of type II 17beta-hydroxysteroid dehydrogenase for the treatment of osteoporosis. (PMID 16806919). Phenylpropiolic acid (C6H5CCCO2H) is formed by the action of alcoholic potash on cinnamic acid dibromide (C6H5CHBrCHBrCO2H), crystallizes in long needles or prisms which melt at 136–137 °C. When heated with water to 120 °C, it yields phenylacetylene (C6H5CCH). Chromic acid oxidizes it to benzoic acid; zinc and acetic acid reduce it to cinnamic acid, C6H5CH=CHCO2H, whilst sodium amalgam reduces it to hydrocinnamic acid, C6H5CH2CH2CO2H. Ortho-nitrophenylpropiolic acid, NO2C6H4CCCO2H, prepared by the action of alcoholic potash on ortho-nitrocinnamic acid dibromide, crystallizes in needles which decompose when heated to 155–156 °C. It is readily converted into indigo.
Phenylpropiolic acid is one of a number of phenylpropanoid, natural products occurring in plants pathways involved in plant resistance providing building units of physical barriers against pathogen invasion, synthesizing an array of antibiotic compounds, and producing signals implicated in the mounting of plant resistance. (PMID 15199968)
Phenylpropiolic acid is an endogenous metabolite. Phenylpropiolic acid is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Phenylpropiolic acid is an endogenous metabolite. Phenylpropiolic acid is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

同义名列表

30 个代谢物同义名

Phenylacetylene monocarboxylic acid; Phenylacetylene monocarboxylate; Phenylacetylenecarboxylic acid; beta-Phenylpropargylic acid; Phenyl-(8ci)propiolic acid; Phenylacetylenecarboxylate; 3-phenylprop-2-ynoic acid; 3-Phenyl-2-propynoic acid; b-Phenylpropargylic acid; Β-phenylpropargylic acid; 3-Phenyl-propiolic acid; beta-Phenylpropargylate; 3-Phenylpropynoic acid; 3-Phenylpropiolic acid; Phenyl-(8ci)propiolate; Phenylpropioplic acid; Phenyl-propiolic acid; 3-Phenyl-2-propynoate; Phenylpropynoic acid; Β-phenylpropargylate; b-Phenylpropargylate; Phenylpropiolic acid; 3-Phenyl-propiolate; 3-Phenylpropiolate; 3-Phenylpropynoate; Phenyl-propiolate; Phenylpropioplate; Phenylpropynoate; Phenylpropiolate; Phenylpropiolic acid



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)

1 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

  • Jun He, Harro J Bouwmeester, Marcel Dicke, Iris F Kappers. Transcriptional and metabolite analysis reveal a shift in direct and indirect defences in response to spider-mite infestation in cucumber (Cucumis sativus). Plant molecular biology. 2020 Jul; 103(4-5):489-505. doi: 10.1007/s11103-020-01005-y. [PMID: 32306368]
  • Isabel Gutiérrez-Díaz, Tania Fernández-Navarro, Nuria Salazar, Begoña Bartolomé, M Victoria Moreno-Arribas, Patricia López, Ana Suárez, Clara G de Los Reyes-Gavilán, Miguel Gueimonde, Sonia González. Could Fecal Phenylacetic and Phenylpropionic Acids Be Used as Indicators of Health Status?. Journal of agricultural and food chemistry. 2018 Oct; 66(40):10438-10446. doi: 10.1021/acs.jafc.8b04102. [PMID: 30227707]
  • Yung-Ping Lee, Tzong-Fu Kuo, Shoei-Sheng Lee. Identification of the metabolites of TCM prescription Sinisan, found in miniature pig urine via intragastric administration. Journal of pharmaceutical and biomedical analysis. 2015; 111(?):311-9. doi: 10.1016/j.jpba.2015.04.011. [PMID: 25931441]
  • Shih-Chia Tso, Xiangbing Qi, Wen-Jun Gui, Jacinta L Chuang, Lorraine K Morlock, Amy L Wallace, Kamran Ahmed, Sunil Laxman, Philippe M Campeau, Brendan H Lee, Susan M Hutson, Benjamin P Tu, Noelle S Williams, Uttam K Tambar, R Max Wynn, David T Chuang. Structure-based design and mechanisms of allosteric inhibitors for mitochondrial branched-chain α-ketoacid dehydrogenase kinase. Proceedings of the National Academy of Sciences of the United States of America. 2013 Jun; 110(24):9728-33. doi: 10.1073/pnas.1303220110. [PMID: 23716694]
  • Elizabeth Joubert, Dalene de Beer, Christiaan J Malherbe, Nina Muller, Susan L Bonnet, Jan H van der Westhuizen, Daneel Ferreira. Occurrence and sensory perception of Z-2-(β-d-glucopyranosyloxy)-3-phenylpropenoic acid in rooibos (Aspalathus linearis). Food chemistry. 2013 Jan; 136(2):1078-85. doi: 10.1016/j.foodchem.2012.09.014. [PMID: 23122165]
  • Iwona Morkunas, Dorota Narożna, Witold Nowak, Sławomir Samardakiewicz, Dorota Remlein-Starosta. Cross-talk interactions of sucrose and Fusarium oxysporum in the phenylpropanoid pathway and the accumulation and localization of flavonoids in embryo axes of yellow lupine. Journal of plant physiology. 2011 Mar; 168(5):424-33. doi: 10.1016/j.jplph.2010.08.017. [PMID: 21056513]
  • Kun Li, Xiu-wu Guo, Yin-shan Guo, Cheng-xiang Li, Hong-gang Xie, Xi-xi Hu, Li-heng Zhang, Ying-ni Sun. [Allelopathy of grape root aqueous extracts]. Ying yong sheng tai xue bao = The journal of applied ecology. 2010 Jul; 21(7):1779-84. doi: . [PMID: 20879537]
  • Priya Ranjan, Yu-Ying Kao, Hongying Jiang, Chandrashekhar P Joshi, Scott A Harding, Chung-Jui Tsai. Suppression subtractive hybridization-mediated transcriptome analysis from multiple tissues of aspen (Populus tremuloides) altered in phenylpropanoid metabolism. Planta. 2004 Aug; 219(4):694-704. doi: 10.1007/s00425-004-1291-9. [PMID: 15146331]
  • Sylvain La Camera, Guillaume Gouzerh, Sandrine Dhondt, Laurent Hoffmann, Bernard Fritig, Michel Legrand, Thierry Heitz. Metabolic reprogramming in plant innate immunity: the contributions of phenylpropanoid and oxylipin pathways. Immunological reviews. 2004 Apr; 198(?):267-84. doi: 10.1111/j.0105-2896.2004.0129.x. [PMID: 15199968]
  • . . . . doi: . [PMID: 15145789]