Salazinic acid (BioDeep_00000319468)

   

natural product


代谢物信息卡片


Salazinic acid

化学式: C18H12O10 (388.0430452)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 32.61%

分子结构信息

SMILES: CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C4=C(C(=C3CO)O)C(=O)OC4O)C=O)O
InChI: InChI=1S/C18H12O10/c1-5-2-8(21)6(3-19)13-9(5)16(23)27-14-7(4-20)12(22)10-11(15(14)26-13)18(25)28-17(10)24/h2-3,18,20-22,25H,4H2,1H3

描述信息

D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates
Origin: Microbe, Carboxylic acids

同义名列表

1 个代谢物同义名

Salazinic acid



数据库引用编号

13 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)

31 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

  • Tatapudi Kiran Kumar, Bandi Siva, Basani Kiranmai, Vidya Jyothi Alli, Surender Singh Jadav, Araveeti Madhusudana Reddy, Joël Boustie, Françoise Le Devehat, Ashok Kumar Tiwari, Katragadda Suresh Babu. Salazinic Acid and Norlobaridone from the Lichen Hypotrachyna cirrhata: Antioxidant Activity, α-Glucosidase Inhibitory and Molecular Docking Studies. Molecules (Basel, Switzerland). 2023 Nov; 28(23):. doi: 10.3390/molecules28237840. [PMID: 38067568]
  • Asshaima Paramita Devi, Thuc-Huy Duong, Solenn Ferron, Mehdi A Beniddir, Minh-Hiep Dinh, Van-Kieu Nguyen, Nguyen-Kim-Tuyen Pham, Dinh-Hung Mac, Joël Boustie, Warinthorn Chavasiri, Pierre Le Pogam. Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum. Planta medica. 2020 Nov; 86(16):1216-1224. doi: 10.1055/a-1203-0623. [PMID: 32819010]
  • Vertika Shukla, D K Patel, Rajesh Bajpai, Manoj Semwal, D K Upreti. Ecological implication of variation in the secondary metabolites in Parmelioid lichens with respect to altitude. Environmental science and pollution research international. 2016 Jan; 23(2):1391-7. doi: 10.1007/s11356-015-5311-z. [PMID: 26370809]
  • Mayurika Goel, Prem Dureja, Archna Rani, Prem L Uniyal, Hartmut Laatsch. Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. Journal of agricultural and food chemistry. 2011 Mar; 59(6):2299-307. doi: 10.1021/jf1049613. [PMID: 21351753]
  • G Amo de Paz, J Raggio, M P Gómez-Serranillos, O M Palomino, E González-Burgos, M E Carretero, A Crespo. HPLC isolation of antioxidant constituents from Xanthoparmelia spp. Journal of pharmaceutical and biomedical analysis. 2010 Oct; 53(2):165-71. doi: 10.1016/j.jpba.2010.04.013. [PMID: 20457504]
  • Rebecca Dailey, Roger Siemion, Merl Raisbeck, Chris Jesse. Analysis of salazinic, norstictic, and usnic acids in Xanthoparmelia chlorochroa by ultra-performance liquid chromatography/tandem mass spectrometry. Journal of AOAC International. 2010 Jul; 93(4):1137-42. doi: NULL. [PMID: 20922944]
  • Bruno Burlando, Elia Ranzato, Andrea Volante, Giovanni Appendino, Federica Pollastro, Luisella Verotta. Antiproliferative effects on tumour cells and promotion of keratinocyte wound healing by different lichen compounds. Planta medica. 2009 May; 75(6):607-13. doi: 10.1055/s-0029-1185329. [PMID: 19199230]