Moupinamide (BioDeep_00000000493)

   

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


(Z,2E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enimidic acid

化学式: C18H19NO4 (313.1314014)
中文名称: N-反式阿魏酰酪胺, N-反式-阿魏酰酪胺
谱图信息: 最多检出来源 Viridiplantae(plant) 0.04%

分子结构信息

SMILES: COC1=C(C=CC(=C1)/C=C/C(=O)NCCC2=CC=C(C=C2)O)O
InChI: InChI=1S/C18H19NO4/c1-23-17-12-14(4-8-16(17)21)5-9-18(22)19-11-10-13-2-6-15(20)7-3-13/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)/b9-5+

描述信息

N-feruloyltyramine is a member of tyramines. It has a role as a metabolite.
Moupinamide is a natural product found in Zanthoxylum beecheyanum, Polyalthia suberosa, and other organisms with data available.
See also: Tobacco Leaf (part of); Cannabis sativa subsp. indica top (part of); Ipomoea aquatica leaf (part of).
Alkaloid from Piper nigrum. Moupinamide is found in many foods, some of which are nutmeg, amaranth, sapodilla, and orange bell pepper.
Moupinamide is found in eggplant. Moupinamide is an alkaloid from Piper nigru
CASMI2013 Challenge_1 MS2 data; [MS1] MSJ00001
CASMI2013 Challenge_1 MS1 data; [MS2] MSJ00002
N-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid from Piper nigru, is an inhibitor of COX1 and COX2, with potential antioxidant properties. N-trans-Feruloyltyramine possesses anti-inflammatory activity[1].
N-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid from Piper nigru, is an inhibitor of COX1 and COX2, with potential antioxidant properties. N-trans-Feruloyltyramine possesses anti-inflammatory activity[1].

同义名列表

34 个代谢物同义名

(Z,2E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enimidic acid; 2-Propenamide, 3-(4-hydroxy-3-methoxyphenyl)-N-(2-(4-hydroxyphenyl)ethyl)-, (2E)-; (2E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-2-propenamide; (E)-3-(4-hydroxy-3-methoxy-phenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide; (2E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide; (E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide; (E)-3-(4-Hydroxy-3-methoxy-phenyl)-N-[2-(4-hydroxy-phenyl)-ethyl]-acrylamide; 2-Propenamide, 3-(4-hydroxy-3-methoxyphenyl)-N-(2-(4-hydroxyphenyl)ethyl)-; (E)-3-(4-HYDROXY-3-METHOXYPHENYL)-N-(4-HYDROXYPHENETHYL)ACRYLAMIDE; (2,3)trans-N-(p-Hydroxyphenethyl)ferulamide; N-P-TRANS-HYDROXYPHENETHYL FERULAMINE; Moupinamide, >=95\\% (LC/MS-ELSD); N-feruloyltyramine; Moupinamide; feruloyltyramine, (E)-isomer; feruloyltyramine, (Z)-isomer; N-Trans-Feruloyl Tyramine; N-trans-Feruloyltyramine; N-[(E)-feruloyl]tyramine; trans-N-Feruloyltyramine; N-Transferuloyl Tyramine; N-Trans-feruloyltramine; (e)-n-feruloyltyramine; N-E-FERULOYL TYRAMINE; (E)-Feruloyltyramine; N-feruloyltyramine; N-FERYROYLTYRAMINE; feruloyl tyramine; feruloyltyramine; UNII-WC99S6JM5Y; MEGxp0_000693; ACon1_001233; moupinamide; Alfrutamide; WC99S6JM5Y



数据库引用编号

25 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(3)

PlantCyc(2)

代谢反应

130 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(4)

WikiPathways(0)

Plant Reactome(3)

INOH(0)

PlantCyc(123)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

414 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

  • Oscar Galarce-Bustos, Camilo Obregón, Alejandro Vallejos-Almirall, Christian Folch, Francisca Acevedo. Application of effect-directed analysis using TLC-bioautography for rapid isolation and identification of antidiabetic compounds from the leaves of Annona cherimola Mill. Phytochemical analysis : PCA. 2023 Jul; ?(?):. doi: 10.1002/pca.3265. [PMID: 37488746]
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  • Martino Forino, Luciana Tartaglione, Carmela Dell'Aversano, Patrizia Ciminiello. NMR-based identification of the phenolic profile of fruits of Lycium barbarum (goji berries). Isolation and structural determination of a novel N-feruloyl tyramine dimer as the most abundant antioxidant polyphenol of goji berries. Food chemistry. 2016 Mar; 194(?):1254-9. doi: 10.1016/j.foodchem.2015.08.129. [PMID: 26471679]
  • Qiulong Zhang, Tao Ma, Na Hu, Chenxi Ding, Yongxin Liang, Wencong Li, Yourui Suo, Chenxu Ding. One Step to Separate Five Alkaloids from Hypecoum leptocarpum by High-Speed Counter-Current Chromatography. Journal of chromatographic science. 2016 Mar; 54(3):466-71. doi: 10.1093/chromsci/bmv153. [PMID: 26499120]
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  • Feras Alali, Tamam El-Elimat, Hanan Albataineh, Qosay Al-Balas, Mohammad Al-Gharaibeh, Joseph O Falkinham, Wei-Lun Chen, Steven M Swanson, Nicholas H Oberlies. Cytotoxic Homoisoflavones from the Bulbs of Bellevalia eigii. Journal of natural products. 2015 Jul; 78(7):1708-15. doi: 10.1021/acs.jnatprod.5b00357. [PMID: 26147490]
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  • Jong Hoon Ahn, Eun Sil Kim, Chul Lee, Soonok Kim, Soo-Hyun Cho, Bang Yeon Hwang, Mi Kyeong Lee. Chemical constituents from Nelumbo nucifera leaves and their anti-obesity effects. Bioorganic & medicinal chemistry letters. 2013 Jun; 23(12):3604-8. doi: 10.1016/j.bmcl.2013.04.013. [PMID: 23642481]
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