Furanodiene (BioDeep_00000860056)

Main id: BioDeep_00000000693

 

PANOMIX_OTCML-2023 natural product Volatile Flavor Compounds


代谢物信息卡片


InChI=1\C15H20O\c1-11-5-4-6-12(2)9-15-14(8-7-11)13(3)10-16-15\h6-7,10H,4-5,8-9H2,1-3H3\b11-7+,12-6

化学式: C15H20O (216.151407)
中文名称: 异莪术呋喃二烯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C/C/1=C\Cc2c(C)coc2C/C(=C/CC1)/C
InChI: InChI=1S/C15H20O/c1-11-5-4-6-12(2)9-15-14(8-7-11)13(3)10-16-15/h6-7,10H,4-5,8-9H2,1-3H3/b11-7+,12-6+

描述信息

同义名列表

9 个代谢物同义名

InChI=1\C15H20O\c1-11-5-4-6-12(2)9-15-14(8-7-11)13(3)10-16-15\h6-7,10H,4-5,8-9H2,1-3H3\b11-7+,12-6; cyclodeca[b]furan, 4,7,8,11-tetrahydro-3,6,10-trimethyl-, (5E)-; (5E,9E)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan; (5E)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan; 3,6,10-Trimethyl-4,7,8,11-tetrahydro-cyclodeca[b]furan; isofuranodiene; Furanodiene; 19912-61-9; Furanodiene



数据库引用编号

16 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)

181 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

  • Valentina Notarstefano, Michela Pisani, Massimo Bramucci, Luana Quassinti, Filippo Maggi, Lisa Vaccari, Marco Parlapiano, Elisabetta Giorgini, Paola Astolfi. A vibrational in vitro approach to evaluate the potential of monoolein nanoparticles as isofuranodiene carrier in MDA-MB 231 breast cancer cell line: New insights from Infrared and Raman microspectroscopies. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2022 Mar; 269(?):120735. doi: 10.1016/j.saa.2021.120735. [PMID: 34923374]
  • Songyot Anuchapreeda, Nattakanwadee Khumpirapang, Kawinnat Rupitiwiriya, Leelawat Tho-Iam, Aroonchai Saiai, Siriporn Okonogi, Toyonobu Usuki. Cytotoxicity and inhibition of leukemic cell proliferation by sesquiterpenes from rhizomes of Mah-Lueang (Curcuma cf. viridiflora Roxb.). Bioorganic & medicinal chemistry letters. 2018 02; 28(3):410-414. doi: 10.1016/j.bmcl.2017.12.029. [PMID: 29274817]
  • Riccardo Petrelli, Farahnaz Ranjbarian, Stefano Dall'Acqua, Fabrizio Papa, Romilde Iannarelli, Stephane L Ngahang Kamte, Sauro Vittori, Giovanni Benelli, Filippo Maggi, Anders Hofer, Loredana Cappellacci. An overlooked horticultural crop, Smyrnium olusatrum, as a potential source of compounds effective against African trypanosomiasis. Parasitology international. 2017 Apr; 66(2):146-151. doi: 10.1016/j.parint.2017.01.001. [PMID: 28087440]
  • Ahmed M Mustafa, Filippo Maggi, Fabrizio Papa, Elif Kaya, Miris Dikmen, Yusuf Öztürk. Isofuranodiene: A neuritogenic compound isolated from wild celery (Smyrnium olusatrum L., Apiaceae). Food chemistry. 2016 Feb; 192(?):782-7. doi: 10.1016/j.foodchem.2015.07.079. [PMID: 26304411]
  • Wenping Li, Jingshan Shi, Fabrizio Papa, Filippo Maggi, Xiuping Chen. Isofuranodiene, the main volatile constituent of wild celery (Smyrnium olusatrum L.), protects d-galactosamin/lipopolysacchride-induced liver injury in rats. Natural product research. 2016; 30(10):1162-5. doi: 10.1080/14786419.2015.1041139. [PMID: 25978596]
  • Fabrizio Papa, Massimo Ricciutelli, Kevin Cianfaglione, Filippo Maggi. Isofuranodiene is the main volatile constituent of Smyrnium perfoliatum L. subsp. perfoliatum growing in central Italy. Natural product research. 2016; 30(3):345-9. doi: 10.1080/14786419.2015.1047777. [PMID: 26134598]
  • Baolian Wang, Shuang Yang, Li Sheng, Yan Li. Simultaneous quantification of curdione, furanodiene and germacrone in rabbit plasma using liquid chromatography-tandem mass spectrometry and its application to a pharmacokinetic study. Biomedical chromatography : BMC. 2015 Sep; 29(9):1393-8. doi: 10.1002/bmc.3436. [PMID: 25678109]
  • Luana Quassinti, Filippo Maggi, Luciano Barboni, Massimo Ricciutelli, Manuela Cortese, Fabrizio Papa, Chiara Garulli, Cristina Kalogris, Sauro Vittori, Massimo Bramucci. Wild celery (Smyrnium olusatrum L.) oil and isofuranodiene induce apoptosis in human colon carcinoma cells. Fitoterapia. 2014 Sep; 97(?):133-41. doi: 10.1016/j.fitote.2014.06.004. [PMID: 24924290]
  • Michela Buccioni, Diego Dal Ben, Catia Lambertucci, Filippo Maggi, Fabrizio Papa, Ajiroghene Thomas, Claudia Santinelli, Gabriella Marucci. Antiproliferative evaluation of isofuranodiene on breast and prostate cancer cell lines. TheScientificWorldJournal. 2014; 2014(?):264829. doi: 10.1155/2014/264829. [PMID: 24967427]
  • Li-Feng Zhang, Tao-Tao Lu, Shu-Qiu Zhang, Wen-Han Lin, Qing-Shan Li. Pharmacokinetics and tissue distribution of furanodiene W/O/W multiple emulsions in rats by a fast and sensitive HPLC-APCI-MS/MS method. Xenobiotica; the fate of foreign compounds in biological systems. 2013 Dec; 43(12):1095-102. doi: 10.3109/00498254.2013.793434. [PMID: 23638824]
  • Meng Chen, Yan Lou, Yaodong Wu, Zhaoke Meng, Liping Li, Lushan Yu, Su Zeng, Hui Zhou, Huidi Jiang. Characterization of in vivo and in vitro metabolites of furanodiene in rats by high performance liquid chromatography-electrospray ionization mass spectrometry and nuclear magnetic resonance spectra. Journal of pharmaceutical and biomedical analysis. 2013 Dec; 86(?):161-8. doi: 10.1016/j.jpba.2013.08.008. [PMID: 23998967]
  • Filippo Maggi, Luciano Barboni, Fabrizio Papa, Giovanni Caprioli, Massimo Ricciutelli, Gianni Sagratini, Sauro Vittori. A forgotten vegetable (Smyrnium olusatrum L., Apiaceae) as a rich source of isofuranodiene. Food chemistry. 2012 Dec; 135(4):2852-62. doi: 10.1016/j.foodchem.2012.07.027. [PMID: 22980882]
  • Lixia Pei, Sheng Liu, Jin Zheng, Xiuping Chen. A sensitive method for determination of furanodiene in rat plasma using liquid chromatography/tandem mass spectrometry and its application to a pharmacokinetic study. Biomedical chromatography : BMC. 2012 Jul; 26(7):826-32. doi: 10.1002/bmc.1736. [PMID: 22052715]
  • Bin Wu, Jun Chen, Haibin Qu, Yiyu Cheng. Complex sesquiterpenoids with tyrosinase inhibitory activity from the leaves of Chloranthus tianmushanensis. Journal of natural products. 2008 May; 71(5):877-80. doi: 10.1021/np070623r. [PMID: 18357995]