Hydroferulic (BioDeep_00000866002)

Main id: BioDeep_00000017611

 

PANOMIX_OTCML-2023


代谢物信息卡片


.beta.-(4-Hydroxy-3-methoxyphenyl)propionic acid

化学式: C10H12O4 (196.0736)
中文名称: 3-(4-羟基-3-甲氧苯基)丙酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=C(C=CC(=C1)CCC(=O)O)O
InChI: InChI=1S/C10H12O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2,4,6,11H,3,5H2,1H3,(H,12,13)

描述信息

Dihydroferulic acid (Hydroferulic acid) is one of the main metabolites of curcumin and antioxidant/radical-scavenging properties with an IC50 value of 19.5 μM. Dihydroferulic acid is a metabolite of human gut microflora as well as a precursor of vanillic acid[1][2].
Dihydroferulic acid (Hydroferulic acid) is one of the main metabolites of curcumin and antioxidant/radical-scavenging properties with an IC50 value of 19.5 μM. Dihydroferulic acid is a metabolite of human gut microflora as well as a precursor of vanillic acid[1][2].

同义名列表

18 个代谢物同义名

.beta.-(4-Hydroxy-3-methoxyphenyl)propionic acid; 3-(4-hydroxy-3-methoxy-phenyl)propionic acid; 3-(4-hydroxy-3-methoxy-phenyl)propanoic acid; Benzenepropanoic acid, 4-hydroxy-3-methoxy-; 3-(4-Hydroxy-3-methoxyphenyl)propanoic acid; 3-(4-Hydroxy-3-methoxyphenyl)propionic acid; Benzenepropanoic acid, 4-hydroxy-3-methoxy; 4-Hydroxy-3-methoxyhydrocinnamic acid; Dihydroconiferylic acid; Dihydroferulic acid; Hydroferulic acid; EINECS 214-489-5; Hydroferulic; AIDS-017866; 17803_FLUKA; ZERO\009218; AIDS017866; 1135-23-5



数据库引用编号

5 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)

13 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。

亚细胞结构定位 关联基因列表


文献列表

  • Gema Baeza, Eva-Maria Bachmair, Sharon Wood, Raquel Mateos, Laura Bravo, Baukje de Roos. The colonic metabolites dihydrocaffeic acid and dihydroferulic acid are more effective inhibitors of in vitro platelet activation than their phenolic precursors. Food & function. 2017 Mar; 8(3):1333-1342. doi: 10.1039/c6fo01404f. [PMID: 28229135]
  • Letizia Bresciani, Francesca Scazzina, Roberto Leonardi, Elisabetta Dall'Aglio, Michael Newell, Margherita Dall'Asta, Camilla Melegari, Sumantra Ray, Furio Brighenti, Daniele Del Rio. Bioavailability and metabolism of phenolic compounds from wholegrain wheat and aleurone-rich wheat bread. Molecular nutrition & food research. 2016 11; 60(11):2343-2354. doi: 10.1002/mnfr.201600238. [PMID: 27273424]
  • Hengye Chen, Muhammad Safiullah Virk, Fusheng Chen. Phenolic acids inhibit the formation of advanced glycation end products in food simulation systems depending on their reducing powers and structures. International journal of food sciences and nutrition. 2016 Jun; 67(4):400-11. doi: 10.3109/09637486.2016.1166187. [PMID: 27102241]
  • Pei Wang, Huadong Chen, Yingdong Zhu, Jennifer McBride, Junsheng Fu, Shengmin Sang. Oat avenanthramide-C (2c) is biotransformed by mice and the human microbiota into bioactive metabolites. The Journal of nutrition. 2015 Feb; 145(2):239-45. doi: 10.3945/jn.114.206508. [PMID: 25644343]
  • Angélique Stalmach, Gary Williamson, Alan Crozier. Impact of dose on the bioavailability of coffee chlorogenic acids in humans. Food & function. 2014 Aug; 5(8):1727-37. doi: 10.1039/c4fo00316k. [PMID: 24947504]
  • Luciano Callipo, Chiara Cavaliere, Valentina Fuscoletti, Riccardo Gubbiotti, Roberto Samperi, Aldo Laganà. Phenilpropanoate identification in young wheat plants by liquid chromatography/tandem mass spectrometry: monomeric and dimeric compounds. Journal of mass spectrometry : JMS. 2010 Sep; 45(9):1026-40. doi: 10.1002/jms.1800. [PMID: 20690165]
  • Fernanda M F Roleira, Christophe Siquet, Elizabeta Orrù, E Manuela Garrido, Jorge Garrido, Nuno Milhazes, Gianni Podda, Fátima Paiva-Martins, Salette Reis, Rui A Carvalho, Elisiário J Tavares da Silva, Fernanda Borges. Lipophilic phenolic antioxidants: correlation between antioxidant profile, partition coefficients and redox properties. Bioorganic & medicinal chemistry. 2010 Aug; 18(16):5816-25. doi: 10.1016/j.bmc.2010.06.090. [PMID: 20650639]
  • Philippe A Guy, Mathieu Renouf, Denis Barron, Christophe Cavin, Fabiola Dionisi, Sunil Kochhar, Serge Rezzi, Gary Williamson, Heike Steiling. Quantitative analysis of plasma caffeic and ferulic acid equivalents by liquid chromatography tandem mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2009 Dec; 877(31):3965-74. doi: 10.1016/j.jchromb.2009.10.006. [PMID: 19879819]
  • E Azzini, R Bugianesi, F Romano, D Di Venere, S Miccadei, A Durazzo, M S Foddai, G Catasta, V Linsalata, G Maiani. Absorption and metabolism of bioactive molecules after oral consumption of cooked edible heads of Cynara scolymus L. (cultivar Violetto di Provenza) in human subjects: a pilot study. The British journal of nutrition. 2007 May; 97(5):963-9. doi: 10.1017/s0007114507617218. [PMID: 17408528]
  • John J Beck, Jong H Kim, Bruce C Campbell, Shen-Chieh Chou. Fungicidal activities of dihydroferulic acid alkyl ester analogues. Journal of natural products. 2007 May; 70(5):779-82. doi: 10.1021/np0606345. [PMID: 17469871]