Lupiwighteone (BioDeep_00000017571)

   

human metabolite PANOMIX_OTCML-2023 natural product


代谢物信息卡片


5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one; 8-Prenylgenistein

化学式: C20H18O5 (338.1154178)
中文名称: 黄羽扇豆魏特酮
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 85.71%

分子结构信息

SMILES: c1(cc(c2c(c1CC=C(C)C)occ(c2=O)c1ccc(cc1)O)O)O
InChI: InChI=1S/C20H18O5/c1-11(2)3-8-14-16(22)9-17(23)18-19(24)15(10-25-20(14)18)12-4-6-13(21)7-5-12/h3-7,9-10,21-23H,8H2,1-2H3

描述信息

Lupiwighteone is a member of isoflavones.
Lupiwighteone is a natural product found in Anthyllis hermanniae, Erythrina sigmoidea, and other organisms with data available.
Isolated from Glycyrrhiza uralensis (Chinese licorice) and Vigna angularis (azuki bean). Lupiwighteone is found in herbs and spices, pulses, and adzuki bean.
Lupiwighteone is found in adzuki bean. Lupiwighteone is isolated from Glycyrrhiza uralensis (Chinese licorice) and Vigna angularis (azuki bean).

同义名列表

19 个代谢物同义名

5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one; 8-Prenylgenistein; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one, 9CI; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-; 4H-1-Benzopyran-4-one,5,7-dihydroxy-3- (4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one; 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-chromen-4-one #; 3-(4-HYDROXYPHENYL)-8-(3-METHYLBUT-2-ENYL)-5,7-BIS(OXIDANYL)CHROMEN-4-ONE; 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one; 5,7,4-Trihydroxy-8-(3,3-dimethylallyl)isoflavone; 5,7,4-Trihydroxy-8-prenylisoflavone; YGCCASGFIOIXIN-UHFFFAOYSA-N; 8-Isopentenylgenistein; 8-prenylgenistein; Lupiwighteone; MEGxp0_000421; S5W46B3BUM



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

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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)

51 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

  • Serhat S Çiçek, Mayra Galarza Pérez, Arlette Wenzel-Storjohann, Roberto M Bezerra, Jorge F O Segovia, Ulrich Girreser, Isamu Kanzaki, Deniz Tasdemir. Antimicrobial Prenylated Isoflavones from the Leaves of the Amazonian Medicinal Plant Vatairea guianensis Aubl. Journal of natural products. 2022 04; 85(4):927-935. doi: 10.1021/acs.jnatprod.1c01035. [PMID: 35271771]
  • Yan Lin, Yi Kuang, Kai Li, Shuang Wang, Wei Song, Xue Qiao, Gulnar Sabir, Min Ye. Screening for bioactive natural products from a 67-compound library of Glycyrrhiza inflata. Bioorganic & medicinal chemistry. 2017 07; 25(14):3706-3713. doi: 10.1016/j.bmc.2017.05.009. [PMID: 28522265]
  • Kai Li, Shuai Ji, Wei Song, Yi Kuang, Yan Lin, Shunan Tang, Zexu Cui, Xue Qiao, Siwang Yu, Min Ye. Glycybridins A-K, Bioactive Phenolic Compounds from Glycyrrhiza glabra. Journal of natural products. 2017 02; 80(2):334-346. doi: 10.1021/acs.jnatprod.6b00783. [PMID: 28140583]
  • Shaopeng Wei, Wenjun Wu, Zhiqin Ji. New antifungal pyranoisoflavone from Ficus tikoua Bur. International journal of molecular sciences. 2012; 13(6):7375-7382. doi: 10.3390/ijms13067375. [PMID: 22837700]
  • Muhammad Shaiq Ali, Muhammad Imran Ali, Patricia A Onocha, Zeeshan Ahmed. bis-Sigmodiol: a new prenylflavanone dimer from Erythrina sigmoidea Hua (Fabaceae) of Nigeria. Journal of Asian natural products research. 2011 Feb; 13(2):182-7. doi: 10.1080/10286020.2010.546352. [PMID: 21279883]
  • A Kumar, S Lingadurai, A Jain, N R Barman. Erythrina variegata Linn: A review on morphology, phytochemistry, and pharmacological aspects. Pharmacognosy reviews. 2010 Jul; 4(8):147-52. doi: 10.4103/0973-7847.70908. [PMID: 22228954]
  • Georg Kretzschmar, Oliver Zierau, Jannette Wober, Sandra Tischer, Peter Metz, Günter Vollmer. Prenylation has a compound specific effect on the estrogenicity of naringenin and genistein. The Journal of steroid biochemistry and molecular biology. 2010 Jan; 118(1-2):1-6. doi: 10.1016/j.jsbmb.2009.08.005. [PMID: 19733663]
  • Yan Zhang, Xiao-Li Li, Xin-Sheng Yao, Man-Sau Wong. Osteogenic activities of genistein derivatives were influenced by the presence of prenyl group at ring A. Archives of pharmacal research. 2008 Dec; 31(12):1534-9. doi: 10.1007/s12272-001-2147-5. [PMID: 19099220]
  • Li Xiaoli, Wang Naili, Wong Man Sau, Albert S C Chen, Yao Xinsheng. Four new isoflavonoids from the stem bark of Erythrina variegata. Chemical & pharmaceutical bulletin. 2006 Apr; 54(4):570-3. doi: 10.1248/cpb.54.570. [PMID: 16595969]
  • Daniela M Biondi, Concetta Rocco, Giuseppe Ruberto. Dihydrostilbene derivatives from Glycyrrhiza glabra leaves. Journal of natural products. 2005 Jul; 68(7):1099-102. doi: 10.1021/np050034q. [PMID: 16038558]
  • Paul Erasto, Gomotsang Bojase-Moleta, Runner R T Majinda. Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus speciosus. Phytochemistry. 2004 Apr; 65(7):875-80. doi: 10.1016/j.phytochem.2004.02.011. [PMID: 15081287]