6a&alpha (BioDeep_00000616160)

Main id: BioDeep_00000018309

 

PANOMIX_OTCML-2023


代谢物信息卡片


4,15,16-trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(17),2(7),3,5,13,15-hexaen-5-ol

化学式: C19H21NO4 (327.14705060000006)
中文名称: 六駁鹼
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC
InChI: InChI=1S/C19H21NO4/c1-22-15-9-12-11(7-14(15)21)6-13-17-10(4-5-20-13)8-16(23-2)19(24-3)18(12)17/h7-9,13,20-21H,4-6H2,1-3H3

描述信息

同义名列表

11 个代谢物同义名

4,15,16-trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(17),2(7),3,5,13,15-hexaen-5-ol; 4H-Dibenzo[de,g]quinolin-9-ol,5,6,6a,7-tetrahydro-1,2,10-trimethoxy-, (6aS)-; 1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol; 9-Hydroxy-1,2,10-trimethoxynoraporphine; 1,2,10-Trimethoxy--Noraporphin-9-ol; (+)-Laurotetanine; Laurotetanine; Laurotetanin; Litsoeine; 6aα Litsoene



数据库引用编号

5 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

  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Gonzalo Fuentes-Barros, Sebastián Castro-Saavedra, Leonel Liberona, Williams Acevedo-Fuentes, Cristian Tirapegui, César Mattar, Bruce K Cassels. Variation of the alkaloid content of Peumus boldus (boldo). Fitoterapia. 2018 Jun; 127(?):179-185. doi: 10.1016/j.fitote.2018.02.020. [PMID: 29454020]
  • Jongmin Ahn, Hee-Sung Chae, Young-Won Chin, Jinwoong Kim. Alkaloids from aerial parts of Houttuynia cordata and their anti-inflammatory activity. Bioorganic & medicinal chemistry letters. 2017 06; 27(12):2807-2811. doi: 10.1016/j.bmcl.2017.04.072. [PMID: 28499733]
  • Ali Bakiri, Jane Hubert, Romain Reynaud, Sylvie Lanthony, Dominique Harakat, Jean-Hugues Renault, Jean-Marc Nuzillard. Computer-Aided 13C NMR Chemical Profiling of Crude Natural Extracts without Fractionation. Journal of natural products. 2017 05; 80(5):1387-1396. doi: 10.1021/acs.jnatprod.6b01063. [PMID: 28414230]
  • I-Chi Hung, Su-Sen Chang, Pei-Chun Chang, Cheng-Chun Lee, Calvin Yu-Chian Chen. Memory enhancement by traditional Chinese medicine?. Journal of biomolecular structure & dynamics. 2013 Dec; 31(12):1411-39. doi: 10.1080/07391102.2012.741052. [PMID: 23249175]
  • Ran Wang, Shengan Tang, Huiyuan Zhai, Hongquan Duan. [Studies on anti-tumor metastatic constituents from Lindera glauca]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 Apr; 36(8):1032-6. doi: . [PMID: 21809579]
  • Qi-Zhi Zhao, Yi-Min Zhao, Ke-Jun Wang. [Alkaloids from the root of Lindera angustifolia]. Yao xue xue bao = Acta pharmaceutica Sinica. 2005 Oct; 40(10):931-4. doi: . [PMID: 16408812]
  • S W Sun, S S Lee, H M Huang. Determination of lauraceous aporphine alkaloids by high-performance liquid chromatography. Journal of pharmaceutical and biomedical analysis. 1996 Jun; 14(8-10):1383-7. doi: 10.1016/0731-7085(95)01715-1. [PMID: 8818061]