Acanthoside B (BioDeep_00000396491)

Main id: BioDeep_00000003892

Secondary id: BioDeep_00001892183

natural product PANOMIX_OTCML-2023


代谢物信息卡片


(2S,3R,4S,5S,6R)-2-[4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxy-phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

化学式: C28H36O13 (580.2155806000001)
中文名称: 刺五加提取物
谱图信息: 最多检出来源 Viridiplantae(natural_products) 27.32%

分子结构信息

SMILES: COC1=C(O[C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)C(OC)=CC([C@]3([H])[C@]4([H])[C@@](CO3)([H])[C@](C5=CC(OC)=C(C(OC)=C5)O)([H])OC4)=C1
InChI: InChI=1S/C28H36O13/c1-34-16-5-12(6-17(35-2)21(16)30)25-14-10-39-26(15(14)11-38-25)13-7-18(36-3)27(19(8-13)37-4)41-28-24(33)23(32)22(31)20(9-29)40-28/h5-8,14-15,20,22-26,28-33H,9-11H2,1-4H3/t14-,15-,20+,22+,23-,24+,25+,26+,28-/m0/s1

描述信息

(+)-syringaresinol beta-D-glucoside is a beta-D-glucoside. It has a role as a metabolite. It is functionally related to a (+)-syringaresinol.
Acanthoside B is a natural product found in Strychnos axillaris, Dalbergia sissoo, and other organisms with data available.
Acanthoside B is a potential bioactive lignan with anti-inflammatory and anti-amnesic activities. Acanthoside B can be used for alzheimer's disease and lung inflammation research[1]
Acanthoside B is a potential bioactive lignan with anti-inflammatory and anti-amnesic activities. Acanthoside B can be used for alzheimer's disease and lung inflammation research[1]

同义名列表

22 个代谢物同义名

(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; 4-[(1S,3aR,4S,6aR)-4-(4-Hydroxy-3,5-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2,6-dimethoxyphenyl beta-D-glucopyranoside; 4-[4-(4-Hydroxy-3,5-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2,6-dimethoxyphenyl hexopyranoside; (7alpha,7alpha,8alpha,8alpha)-4-(beta-D-glucopyranosyloxy)-3,3,5,5-tetramethoxy-7,9:7,9-diepoxylignan-4-ol; (+)-Syringaresinol-4-O-beta-D-glucopyranoside; (+)-Syringaresinol 4-O-beta-glucopyranoside; (+)-Syringaresinol O-beta-D-glucoside; (+)-syringaresinol beta-D-glucoside; Eleutheroside e1; ELEUTHEROSIDEE1; MEGxp0_000366; Acanthoside B; ACon1_001107; (2S,3R,4S,5S,6R)-2-[4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxy-phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxy-phenoxy]-6-methylol-tetrahydropyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxy-phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; (2S,3R,4S,5S,6R)-2-[4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; CHEBI:28603; 7374-79-0; C10890; (+)-Syringaresinol O-beta-D-glucoside



数据库引用编号

25 个数据库交叉引用编号

分类词条

相关代谢途径

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代谢反应

0 个相关的代谢反应过程信息。

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BioCyc(0)

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Plant Reactome(0)

INOH(0)

PlantCyc(0)

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156 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

  • Mun Seok Jo, Seoyoung Lee, Jae Sik Yu, Su Cheol Baek, Young-Chang Cho, Ki Hyun Kim. Megastigmane Derivatives from the Cladodes of Opuntia humifusa and Their Nitric Oxide Inhibitory Activities in Macrophages. Journal of natural products. 2020 03; 83(3):684-692. doi: 10.1021/acs.jnatprod.9b01120. [PMID: 32118424]
  • Ning Li, Ying Wang, Xuezheng Li, Hong Zhang, Di Zhou, Wenli Wang, Wei Li, Xiangrong Zhang, Xinyu Li, Yue Hou, Dali Meng. Bioactive phenols as potential neuroinflammation inhibitors from the leaves of Xanthoceras sorbifolia Bunge. Bioorganic & medicinal chemistry letters. 2016 10; 26(20):5018-5023. doi: 10.1016/j.bmcl.2016.08.094. [PMID: 27623545]
  • Le Duc Dat, Nguyen Phuong Thao, Bui Huu Tai, Bui Thi Thuy Luyen, Sohyun Kim, Jung Eun Koo, Young Sang Koh, Nguyen The Cuong, Nguyen Van Thanh, Nguyen Xuan Cuong, Nguyen Hoai Nam, Phan Van Kiem, Chau Van Minh, Young Ho Kim. Chemical constituents from Kandelia candel with their inhibitory effects on pro-inflammatory cytokines production in LPS-stimulated bone marrow-derived dendritic cells (BMDCs). Bioorganic & medicinal chemistry letters. 2015 Apr; 25(7):1412-6. doi: 10.1016/j.bmcl.2015.02.048. [PMID: 25769817]
  • Longshan Zhao, Qi An, Feng Qin, ZhiLi Xiong. Simultaneous determination of six constituents in the fruit of Acanthopanax sessiliflorus (Rupr. et Maxim.) Seem. by HPLC-UV. Natural product research. 2014; 28(7):500-2. doi: 10.1080/14786419.2013.877904. [PMID: 24438013]
  • Preety Dixit, Raju Chillara, Vikram Khedgikar, Jyoti Gautam, Priyanka Kushwaha, Avinash Kumar, Divya Singh, Ritu Trivedi, Rakesh Maurya. Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity. Bioorganic & medicinal chemistry letters. 2012 Jan; 22(2):890-7. doi: 10.1016/j.bmcl.2011.12.036. [PMID: 22212722]
  • Tao Yuan, Chunpeng Wan, Antonio González-Sarrías, Vamsikrishna Kandhi, Nadja B Cech, Navindra P Seeram. Phenolic glycosides from sugar maple (Acer saccharum) bark. Journal of natural products. 2011 Nov; 74(11):2472-6. doi: 10.1021/np200678n. [PMID: 22032697]
  • Prathan Luecha, Kaoru Umehara, Toshio Miyase, Hiroshi Noguchi. Antiestrogenic constituents of the Thai medicinal plants Capparis flavicans and Vitex glabrata. Journal of natural products. 2009 Nov; 72(11):1954-9. doi: 10.1021/np9006298. [PMID: 19943620]