Odoratin (BioDeep_00000269809)

   

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


7-Hydroxy-3- (3-hydroxy-4-methoxyphenyl) -6-methoxy-4H-1-benzopyran-4-one

化学式: C17H14O6 (314.079)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=CC2OC=C(C3C=CC(OC)=C(O)C=3)C(=O)C=2C=C1OC
InChI: InChI=1S/C17H14O6/c1-21-14-4-3-9(5-12(14)18)11-8-23-15-7-13(19)16(22-2)6-10(15)17(11)20/h3-8,18-19H,1-2H3

描述信息

同义名列表

2 个代谢物同义名

Odoratin; 7-Hydroxy-3- (3-hydroxy-4-methoxyphenyl) -6-methoxy-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)

38 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

  • Yan Song, Lan Pan, Wenjie Li, Yingying Si, Di Zhou, Chengjian Zheng, Xiaofang Hao, Xinyue Jia, Yuemei Jia, Minghui Shi, Xiaoguang Jia, Ning Li, Yue Hou. Natural neuro-inflammatory inhibitors from Caragana turfanensis. Bioorganic & medicinal chemistry letters. 2017 10; 27(20):4765-4769. doi: 10.1016/j.bmcl.2017.08.047. [PMID: 28911817]
  • Di Zhou, Hongyan Wei, Zhe Jiang, Xuezheng Li, Kun Jiao, Xiaoguang Jia, Yue Hou, Ning Li. Natural potential neuroinflammatory inhibitors from Alhagi sparsifolia Shap. Bioorganic & medicinal chemistry letters. 2017 02; 27(4):973-978. doi: 10.1016/j.bmcl.2016.12.075. [PMID: 28073678]
  • Yu-Long Zheng, Yu-Long Feng, Li-Kun Zhang, Ragan M Callaway, Alfonso Valiente-Banuet, Du-Qiang Luo, Zhi-Yong Liao, Yan-Bao Lei, Gregor F Barclay, Carlos Silva-Pereyra. Integrating novel chemical weapons and evolutionarily increased competitive ability in success of a tropical invader. The New phytologist. 2015 Feb; 205(3):1350-1359. doi: 10.1111/nph.13135. [PMID: 25367824]
  • Pilar Puebla, Yoko Oshima-Franco, Luiz M Franco, Marcio G Dos Santos, Renata V da Silva, Leandro Rubem-Mauro, Arturo San Feliciano. Chemical constituents of the bark of Dipteryx alata vogel, an active species against Bothrops jararacussu venom. Molecules (Basel, Switzerland). 2010 Nov; 15(11):8193-204. doi: 10.3390/molecules15118193. [PMID: 21076386]
  • Jeong Mi Kim, Ryeo Kyeong Ko, Duk Sang Jung, Sang Suk Kim, Nam Ho Lee. Tyrosinase inhibitory constituents from the stems of Maackia fauriei. Phytotherapy research : PTR. 2010 Jan; 24(1):70-5. doi: 10.1002/ptr.2870. [PMID: 19441007]
  • Cheng Xiang, Jun Cheng, Hong Liang, Yu-Ying Zhao, Jie Feng. [Isoflavones from Millettia nitida var. hirsutissima]. Yao xue xue bao = Acta pharmaceutica Sinica. 2009 Feb; 44(2):158-61. doi: ". [PMID: 19408686]
  • Da-You Ma, Chang-Qi Hu. [Studies on chemical constituents from roots of Caragana sinica]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2008 Mar; 33(5):517-21. doi: ". [PMID: 18536372]
  • X D Luo, S H Wu, Y B Ma, D G Wu. A new triterpenoid from Azadirachta indica. Fitoterapia. 2000 Dec; 71(6):668-72. doi: 10.1016/s0367-326x(00)00230-6. [PMID: 11077174]
  • A R Gaspar, J A Verschoor, A W Neitz, N M Vermeulen. The influence of the sesquiterpene lactones from Geigeria on mast cell degranulation. Biochemical pharmacology. 1987 Aug; 36(15):2461-5. doi: 10.1016/0006-2952(87)90517-x. [PMID: 2440443]