Lirioresinol b (BioDeep_00000395622)

   

PANOMIX_OTCML-2023


代谢物信息卡片


PHENOL, 4,4-(TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2,6-DIMETHOXY-, (1R-(1.ALPHA.,3A.ALPHA.,4.ALPHA.,6A.ALPHA.))-

化学式: C22H26O8 (418.1627596)
中文名称: (-)-丁香树脂酚, (-)-丁香脂素
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC
InChI: InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3/t13-,14-,21+,22+/m1/s1

描述信息

(-)-syringaresinol is the (7beta,7beta,8beta,8beta)-stereoisomer of syringaresinol. It is an enantiomer of a (+)-syringaresinol.
(-)-Syringaresinol is a natural product found in Pittosporum illicioides, Cinnamomum kotoense, and other organisms with data available.
The (7beta,7beta,8beta,8beta)-stereoisomer of syringaresinol.
(-)-Syringaresinol, found in stems of Annona Montana, possesses anti-cancer activity[1].
(-)-Syringaresinol, found in stems of Annona Montana, possesses anti-cancer activity[1].

同义名列表

19 个代谢物同义名

PHENOL, 4,4-(TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2,6-DIMETHOXY-, (1R-(1.ALPHA.,3A.ALPHA.,4.ALPHA.,6A.ALPHA.))-; 4-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxy-phenol; 4-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenol; Phenol, 4,4-(tetrahydro-1H,3H-furo(3,4-C)furan-1,4-diyl)bis(2,6-dimethoxy-, (1R-(1alpha,3aalpha,4alpha,6aalpha))-; Phenol, 4,4-((1R,3aS,4R,6aS)-tetrahydro-1H,3H-furo(3,4-C)furan-1,4-diyl)bis(2,6-dimethoxy-; 4,4-((1R,3aS,4R,6aS)-Tetrahydro-1H,3H-furo(3,4-C)furan-1,4-diyl)bis(2,6-dimethoxyphenol); 4,4-(1R,3aS,4R,6aS)-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol); (7beta,7beta,8beta,8beta)-3,3,5,5-tetramethoxy-7,9:7,9-diepoxylignane-4,4-diol; KOWMJRJXZMEZLD-WRMVBYCNSA-N; Syringaresinol - 93\\%; minus Syringaresinol; Syringaresinol, (-)-; ()-Syringaresinol;; (-)-Lirioresinol B; (-)-Syringaresinol; DL-Syringaresinol; UNII-QD6NNG8CM5; Lirioresinol b; QD6NNG8CM5



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

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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)

COVID-19 Disease Map(0)

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60 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

  • Yan Song, Lan Pan, Wenjie Li, Yingying Si, Di Zhou, Chengjian Zheng, Xiaofang Hao, Xinyue Jia, Yuemei Jia, Minghui Shi, Xiaoguang Jia, Ning Li, Yue Hou. Natural neuro-inflammatory inhibitors from Caragana turfanensis. Bioorganic & medicinal chemistry letters. 2017 10; 27(20):4765-4769. doi: 10.1016/j.bmcl.2017.08.047. [PMID: 28911817]
  • Kyeong Wan Woo, Won Se Suh, Lalita Subedi, Sun Yeou Kim, Aejung Kim, Kang Ro Lee. Bioactive lignan derivatives from the stems of Firmiana simplex. Bioorganic & medicinal chemistry letters. 2016 Feb; 26(3):730-733. doi: 10.1016/j.bmcl.2016.01.008. [PMID: 26774654]
  • Hyun Woo Park, Si Young Cho, Hyun Hee Kim, Bong Sik Yun, Jeong Un Kim, Sang Jun Lee, Jiyong Park. Enantioselective induction of SIRT1 gene by syringaresinol from Panax ginseng berry and Acanthopanax senticosus Harms stem. Bioorganic & medicinal chemistry letters. 2015 Jan; 25(2):307-9. doi: 10.1016/j.bmcl.2014.11.045. [PMID: 25479772]
  • Blanca M Reyes, María Teresa Ramírez-Apan, Rubén A Toscano, Guillermo Delgado. Triterpenes from Garcia parviflora. Cytotoxic evaluation of natural and semisynthetic friedelanes. Journal of natural products. 2010 Nov; 73(11):1839-45. doi: 10.1021/np100440p. [PMID: 20958014]
  • Xiao-Ming Tian, Shi-Zhong Chen, Peng-Fei Tu, Lian-Di Lei. [Studies on chemical constituents of aerial parts of Ammopiptanthus mongolicus]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2008 Oct; 33(19):2204-6. doi: . [PMID: 19166007]
  • Tsung-Hsien Chou, Ih-Sheng Chen, Tsong-Long Hwang, Tai-Chi Wang, Tzong-Huei Lee, Lin-Yang Cheng, Ya-Chih Chang, Jui-Ying Cho, Jih-Jung Chen. Phthalides from Pittosporum illicioides var. illicioides with inhibitory activity on superoxide generation and elastase release by neutrophils. Journal of natural products. 2008 Oct; 71(10):1692-5. doi: 10.1021/np8004503. [PMID: 18817445]
  • Jih-Jung Chen, Tzu-Ying Wang, Tsong-Long Hwang. Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae. Journal of natural products. 2008 Feb; 71(2):212-7. doi: 10.1021/np070594k. [PMID: 18211005]
  • Yong Deuk Min, Sang Un Choi, Kang Ro Lee. Aporphine alkaloids and their reversal activity of multidrug resistance (MDR) from the stems and rhizomes of Sinomenium acutum. Archives of pharmacal research. 2006 Aug; 29(8):627-32. doi: 10.1007/bf02968246. [PMID: 16964757]
  • Dae Sik Jang, Muriel Cuendet, Bao-Ning Su, Steven Totura, Soedarsono Riswan, Harry H Fong, John M Pezzuto, A Douglas Kinghorn. Constituents of the seeds of Hernandia ovigera with inhibitory activity against cyclooxygenase-2. Planta medica. 2004 Oct; 70(10):893-6. doi: 10.1055/s-2004-832612. [PMID: 15490314]
  • H J Zhang, P A Tamez, D H Vu, T T Ghee, V H Nguyen, T X Le, M H Le, M C Nguyen, T T Do, D D Soejarto, H H Fong, J M Pezzuto. Antimalarial compounds from Rhaphidophora decursiva. Journal of natural products. 2001 Jun; 64(6):772-7. doi: 10.1021/np010037c. [PMID: 11421741]