Cudraflavone C (BioDeep_00000266437)

   

PANOMIX_OTCML-2023


代谢物信息卡片


2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-3,6-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one

化学式: C25H26O6 (422.17292960000003)
中文名称:
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 6%

分子结构信息

SMILES: C12C(=O)C(C/C=C(\C)/C)=C(C3C=CC(O)=CC=3O)OC=1C=C(O)C(C/C=C(\C)/C)=C2O
InChI: InChI=1S/C25H26O6/c1-13(2)5-8-16-20(28)12-21-22(23(16)29)24(30)18(9-6-14(3)4)25(31-21)17-10-7-15(26)11-19(17)27/h5-7,10-12,26-29H,8-9H2,1-4H3

描述信息

A tetrahydroxyflavone that is flavone substituted by hydroxy groups at positions 5, 7, 2 and 4 and prenyl groups at positions 3 and 6. Isolated from Morus nigra, it exhibits antibacterial and cytotoxic activities.

同义名列表

3 个代谢物同义名

Cudraflavone C; 2,4,5,7-Tetrahydroxy-3,6-bis(3-methyl-2-butenyl)flavone; 2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-3,6-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one



数据库引用编号

9 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)

0 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

  • Murugan Thulasi Meenu, Grace Kaul, Manjulika Shukla, Kokkuvayil Vasu Radhakrishnan, Sidharth Chopra. Cudraflavone C from Artocarpus hirsutus as a Promising Inhibitor of Pathogenic, Multidrug-Resistant S. aureus, Persisters, and Biofilms: A New Insight into a Rational Explanation of Traditional Wisdom. Journal of natural products. 2021 10; 84(10):2700-2708. doi: 10.1021/acs.jnatprod.1c00578. [PMID: 34546736]
  • Yan-Qiong Guo, Gui-Hua Tang, Lan-Lan Lou, Wei Li, Bei Zhang, Bo Liu, Sheng Yin. Prenylated flavonoids as potent phosphodiesterase-4 inhibitors from Morus alba: Isolation, modification, and structure-activity relationship study. European journal of medicinal chemistry. 2018 Jan; 144(?):758-766. doi: 10.1016/j.ejmech.2017.12.057. [PMID: 29291443]
  • Hsien-Chuen Soo, Felicia Fei-Lei Chung, Kuan-Hon Lim, Veronica Alicia Yap, Tracey D Bradshaw, Ling-Wei Hii, Si-Hoey Tan, Sze-Jia See, Yuen-Fen Tan, Chee-Onn Leong, Chun-Wai Mai. Cudraflavone C Induces Tumor-Specific Apoptosis in Colorectal Cancer Cells through Inhibition of the Phosphoinositide 3-Kinase (PI3K)-AKT Pathway. PloS one. 2017; 12(1):e0170551. doi: 10.1371/journal.pone.0170551. [PMID: 28107519]
  • Sukanya Dej-Adisai, Imron Meechai, Jindaporn Puripattanavong, Sopa Kummee. Antityrosinase and antimicrobial activities from Thai medicinal plants. Archives of pharmacal research. 2014 Apr; 37(4):473-83. doi: 10.1007/s12272-013-0198-z. [PMID: 23835832]
  • Xiao Hu, Jin-Wei Wu, Xiao-Dong Zhang, Qin-Shi Zhao, Jian-Ming Huang, He-Yao Wang, Ai-Jun Hou. Isoprenylated flavonoids and adipogenesis-promoting constituents from Morus nigra. Journal of natural products. 2011 Apr; 74(4):816-24. doi: 10.1021/np100907d. [PMID: 21401118]
  • Ah-Reum Han, You-Jin Kang, Tri Windono, Sang Kook Lee, Eun-Kyoung Seo. Prenylated flavonoids from the heartwood of Artocarpus communis with inhibitory activity on lipopolysaccharide-induced nitric oxide production. Journal of natural products. 2006 Apr; 69(4):719-21. doi: 10.1021/np0600346. [PMID: 16643064]
  • A Groweiss, J H Cardellina, M R Boyd. HIV-Inhibitory prenylated xanthones and flavones from Maclura tinctoria. Journal of natural products. 2000 Nov; 63(11):1537-9. doi: 10.1021/np000175m. [PMID: 11087602]