Pseudoginsenoside_F11 (BioDeep_00000230934)

 

Secondary id: BioDeep_00000018767, BioDeep_00000402912, BioDeep_00000623524

PANOMIX_OTCML-2023


代谢物信息卡片


(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol

化学式: C42H72O14 (800.4921812)
中文名称: 拟人参皂苷 F11, 伪人参皂苷 F11, 拟人参皂苷F11, 拟人参皂苷 F11
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 83.33%

分子结构信息

SMILES: CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C6(CCC(O6)C(C)(C)O)C)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O)O)O
InChI: InChI=1S/C42H72O14/c1-19-28(46)30(48)32(50)35(52-19)55-33-31(49)29(47)23(18-43)54-36(33)53-22-17-41(8)24(39(6)13-11-25(45)37(2,3)34(22)39)16-21(44)27-20(10-14-40(27,41)7)42(9)15-12-26(56-42)38(4,5)51/h19-36,43-51H,10-18H2,1-9H3/t19-,20-,21+,22-,23+,24+,25-,26+,27-,28-,29+,30+,31-,32+,33+,34-,35-,36+,39+,40+,41+,42-/m0/s1

描述信息

Pseudoginsenoside FII is a natural product found in Panax quinquefolius with data available.
Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice.
Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice.

同义名列表

9 个代谢物同义名

(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol; beta-D-Glucopyranoside, (3beta,6alpha,12beta,24R)-20,24-epoxy-3,12,25-trihydroxydammaran-6-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-; (3b,6a,12b,24R)-20,24-Epoxy-3,12,25-trihydroxydammaran-6-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside; pseudoginsenoside-F11; Pseudoginsenoside FII; pseudoginsenoside F11; GINSENOSIDE A1; PF 11; Pseudoginsenoside



数据库引用编号

8 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)

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

  • Hui Xiong, Ai-Hua Zhang, Qi-Qi Zhao, Guang-Li Yan, Hui Sun, Xi-Jun Wang. Discovery of quality-marker ingredients of Panax quinquefolius driven by high-throughput chinmedomics approach. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2020 Aug; 74(?):152928. doi: 10.1016/j.phymed.2019.152928. [PMID: 31451286]
  • Zhen Zhang, Jingyu Yang, Chen Liu, Jun Xie, Shi Qiu, Xue Yang, Chunfu Wu. Pseudoginsenoside-F11 alleviates cognitive deficits and Alzheimer's disease-type pathologies in SAMP8 mice. Pharmacological research. 2019 01; 139(?):512-523. doi: 10.1016/j.phrs.2018.10.024. [PMID: 30394318]
  • Yujie Chen, Zhongzhen Zhao, Hubiao Chen, Tao Yi, Minjian Qin, Zhitao Liang. Chemical differentiation and quality evaluation of commercial Asian and American ginsengs based on a UHPLC-QTOF/MS/MS metabolomics approach. Phytochemical analysis : PCA. 2015 Mar; 26(2):145-60. doi: 10.1002/pca.2546. [PMID: 25448530]
  • Hongbo Wang, Liang Kong, Jianqiao Zhang, Guohua Yu, Guangyao Lv, Fangxi Zhang, Xiaoguang Chen, Jingwei Tian, Fenghua Fu. The pseudoginsenoside F11 ameliorates cisplatin-induced nephrotoxicity without compromising its anti-tumor activity in vivo. Scientific reports. 2014 May; 4(?):4986. doi: 10.1038/srep04986. [PMID: 24832194]
  • Liang Dong, Cui-ying Zhang, Shi-lin Chen. [HPLC-UV-ELSD characteristic figure and chemical pattern recognition of Panacis Quinquefolii Radix]. Yao xue xue bao = Acta pharmaceutica Sinica. 2011 Feb; 46(2):198-202. doi: ". [PMID: 21542292]
  • Li Li, Guo-An Luo, Qiong-Lin Liang, Ping Hu, Yi-Ming Wang. Rapid qualitative and quantitative analyses of Asian ginseng in adulterated American ginseng preparations by UPLC/Q-TOF-MS. Journal of pharmaceutical and biomedical analysis. 2010 May; 52(1):66-72. doi: 10.1016/j.jpba.2009.12.017. [PMID: 20079592]
  • Chun Fu Wu, Yan Li Liu, Ming Song, Wen Liu, Jin Hui Wang, Xian Li, Jing Yu Yang. Protective effects of pseudoginsenoside-F11 on methamphetamine-induced neurotoxicity in mice. Pharmacology, biochemistry, and behavior. 2003 Aug; 76(1):103-9. doi: 10.1016/s0091-3057(03)00215-6. [PMID: 13679222]
  • J H Wang, X Li. [Study on the metabolism of psuedo-ginsenoside F11 in rats]. Yao xue xue bao = Acta pharmaceutica Sinica. 2001 Jun; 36(6):427-31. doi: . [PMID: 12585126]