Pueraria glycoside 3 (BioDeep_00000246869)

 

Secondary id: BioDeep_00000230245

PANOMIX_OTCML-2023


代谢物信息卡片


8- (beta-D-Glucopyranosyloxy) -3,7-dihydroxy-4-methoxyisoflavone

化学式: C22H22O10 (446.1212912)
中文名称: 3-甲氧基葛根素, 3'-甲氧基葛根素
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c1(ccc2c(c1[C@H]1[C@@H]([C@H]([C@@H]([C@@H](O1)CO)O)O)O)occ(c2=O)c1ccc(c(c1)OC)O)O
InChI: InChI=1S/C22H22O10/c1-30-14-6-9(2-4-12(14)24)11-8-31-21-10(17(11)26)3-5-13(25)16(21)22-20(29)19(28)18(27)15(7-23)32-22/h2-6,8,15,18-20,22-25,27-29H,7H2,1H3/t15-,18+,19-,20+,22-/m0/s1

描述信息

3'-Methoxypuerarin (3'-MOP) is an isoflavone extracted from radix puerariae that shows neuron protection activity.
3'-Methoxypuerarin (3'-MOP) is an isoflavone extracted from radix puerariae that shows neuron protection activity.

同义名列表

5 个代谢物同义名

Pueraria glycoside 3; 8- (beta-D-Glucopyranosyloxy) -3,7-dihydroxy-4-methoxyisoflavone; 3-Methoxy Puerarin; 3-Methoxypuerarin; 3'-Methoxypuerarin



数据库引用编号

7 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)

1 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

  • Yingjie Sun, Hongmin Zhang, Ming Cheng, Shijie Cao, Miao Qiao, Boli Zhang, Liqin Ding, Feng Qiu. New hepatoprotective isoflavone glucosides from Pueraria lobata (Willd.) Ohwi. Natural product research. 2019 Dec; 33(24):3485-3492. doi: 10.1080/14786419.2018.1484461. [PMID: 29968479]
  • Yi Tao, Xi Chen, Yanhui Jiang, Baochang Cai. A UPLC-MS/MS approach for simultaneous determination of eight flavonoids in rat plasma, and its application to pharmacokinetic studies of Fu-Zhu-Jiang-Tang tablet in rats. Biomedical chromatography : BMC. 2017 Mar; 31(3):. doi: 10.1002/bmc.3828. [PMID: 27569047]
  • Zhiguo Yu, Xiaoxia Gao, Yunli Zhao, Kaishun Bi. HPLC determination of safflor yellow A and three active isoflavones from TCM Naodesheng in rat plasma and tissues and its application to pharmacokinetic studies. Biomedical chromatography : BMC. 2007 Jun; 21(6):577-84. doi: 10.1002/bmc.764. [PMID: 17385809]
  • Jong Min Kim, Yun Mi Lee, Ga Young Lee, Dae Sik Jang, Ki Hwan Bae, Jin Sook Kim. Constituents of the roots of Pueraria lobata inhibit formation of advanced glycation end products (AGEs). Archives of pharmacal research. 2006 Oct; 29(10):821-5. doi: 10.1007/bf02973900. [PMID: 17121174]
  • J D Baty, P R Robinson, J Wharton. A method for the estimation of acetanilide, paracetamol and phenacetin in plasma and urine using mass fragmentography. Biomedical mass spectrometry. 1976 Apr; 3(2):60-3. doi: 10.1002/bms.1200030204. [PMID: 5162]