CHEBI:28678 (BioDeep_00000864294)

Main id: BioDeep_00000003746

 

PANOMIX_OTCML-2023


代谢物信息卡片


4,7-dihydroxy-2-methoxy-9,10-dihydrophenanthrene

化学式: C15H14O3 (242.0942894)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O
InChI: InChI=1S/C15H14O3/c1-18-12-7-10-3-2-9-6-11(16)4-5-13(9)15(10)14(17)8-12/h4-8,16-17H,2-3H2,1H3

描述信息

同义名列表

5 个代谢物同义名

4,7-dihydroxy-2-methoxy-9,10-dihydrophenanthrene; 7-Methoxy-9,10-dihydrophenanthrene-2,5-diol; CHEBI:28678; 87530-30-1; C10257



数据库引用编号

4 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)

14 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

  • Xiaowen Tang, Qi Liao, Qinqin Li, Linshan Jiang, Wei Li, Jie Xu, Aizhen Xiong, Rufeng Wang, Jing Zhao, Zhengtao Wang, Lili Ding, Li Yang. Lusianthridin ameliorates high fat diet-induced metabolic dysfunction-associated fatty liver disease via activation of FXR signaling pathway. European journal of pharmacology. 2024 Feb; 965(?):176196. doi: 10.1016/j.ejphar.2023.176196. [PMID: 38006926]
  • Tao Li, Weixia Wang, Shumei Li, Cuiping Gong. Lusianthridin Exerts Streptozotocin-Induced Gestational Diabetes Mellitus in Female Rats via Alteration of TLR4/MyD88/NF-κB Signaling Pathway. Journal of oleo science. 2023 Aug; 72(8):775-785. doi: 10.5650/jos.ess23066. [PMID: 37468270]
  • Matthew J Sanders, Yann Ratinaud, Katyayanee Neopane, Nicolas Bonhoure, Emily A Day, Olivier Ciclet, Steve Lassueur, Martine Naranjo Pinta, Maria Deak, Benjamin Brinon, Stefan Christen, Gregory R Steinberg, Denis Barron, Kei Sakamoto. Natural (dihydro)phenanthrene plant compounds are direct activators of AMPK through its allosteric drug and metabolite-binding site. The Journal of biological chemistry. 2022 05; 298(5):101852. doi: 10.1016/j.jbc.2022.101852. [PMID: 35331736]
  • Zhengcai Ju, Qi Liao, Yuangui Yang, Huida Guan, Chao Ma, Xiaowen Tang, Li Yang, Zhengtao Wang. Identification of lusianthridin metabolites in rat liver microsomes by liquid chromatography combined with electrospray ionization time-of-flight mass spectrometry. Biomedical chromatography : BMC. 2021 Mar; 35(3):e5001. doi: 10.1002/bmc.5001. [PMID: 33063881]
  • Zhengcai Ju, Xiaowen Tang, Qi Liao, Huida Guan, Li Yang, Zhengtao Wang. Pharmacokinetic, bioavailability, and metabolism studies of lusianthridin, a dihydrophenanthrene compound, in rats by liquid chromatography/electrospray ionization tandem mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2021 Feb; 195(?):113836. doi: 10.1016/j.jpba.2020.113836. [PMID: 33358433]
  • May Thazin Thant, Nutputsorn Chatsumpun, Wanwimon Mekboonsonglarp, Boonchoo Sritularak, Kittisak Likhitwitayawuid. New Fluorene Derivatives from Dendrobium gibsonii and Their α-Glucosidase Inhibitory Activity. Molecules (Basel, Switzerland). 2020 Oct; 25(21):. doi: 10.3390/molecules25214931. [PMID: 33113779]
  • Chalermporn Sarakulwattana, Wanwimon Mekboonsonglarp, Kittisak Likhitwitayawuid, Pornchai Rojsitthisak, Boonchoo Sritularak. New bisbibenzyl and phenanthrene derivatives from Dendrobium scabrilingue and their α-glucosidase inhibitory activity. Natural product research. 2020 Jun; 34(12):1694-1701. doi: 10.1080/14786419.2018.1527839. [PMID: 30580616]
  • Barbara Tóth, Judit Hohmann, Andrea Vasas. Phenanthrenes: A Promising Group of Plant Secondary Metabolites. Journal of natural products. 2018 03; 81(3):661-678. doi: 10.1021/acs.jnatprod.7b00619. [PMID: 29280630]
  • Ya-Ping Wu, Wen-Jian Liu, Wen-Jun Zhong, Yue-Juan Chen, Dan-Na Chen, Feng He, Lin Jiang. Phenolic compounds from the stems of Flickingeria fimbriata. Natural product research. 2017 Jul; 31(13):1518-1522. doi: 10.1080/14786419.2017.1278599. [PMID: 28278646]
  • Xue-Ming Zhou, Cai-Juan Zheng, Li-She Gan, Guang-Ying Chen, Xiao-Peng Zhang, Xiao-Ping Song, Gao-Nan Li, Chong-Ge Sun. Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile. Journal of natural products. 2016 07; 79(7):1791-7. doi: 10.1021/acs.jnatprod.6b00252. [PMID: 27310249]
  • Ji Sang Hwang, Seon A Lee, Seong Su Hong, Xiang Hua Han, Chul Lee, Shin Jung Kang, Dongho Lee, Youngsoo Kim, Jin Tae Hong, Mi Kyeong Lee, Bang Yeon Hwang. Phenanthrenes from Dendrobium nobile and their inhibition of the LPS-induced production of nitric oxide in macrophage RAW 264.7 cells. Bioorganic & medicinal chemistry letters. 2010 Jun; 20(12):3785-7. doi: 10.1016/j.bmcl.2010.04.054. [PMID: 20483604]
  • Min Hye Yang, Kee Dong Yoon, Young-Won Chin, Ju Hyun Park, Jinwoong Kim. Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita. Bioorganic & medicinal chemistry. 2009 Apr; 17(7):2689-94. doi: 10.1016/j.bmc.2009.02.057. [PMID: 19303782]
  • Hyekyung Yang, Sang Hyun Sung, Young Choong Kim. Antifibrotic phenanthrenes of Dendrobium nobile stems. Journal of natural products. 2007 Dec; 70(12):1925-9. doi: 10.1021/np070423f. [PMID: 18052323]
  • Yanet Hernández-Romero, Juana-Isela Rojas, Rafael Castillo, Alejandra Rojas, Rachel Mata. Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii. Journal of natural products. 2004 Feb; 67(2):160-7. doi: 10.1021/np030303h. [PMID: 14987052]