CHEBI:2015 (BioDeep_00000870634)

Main id: BioDeep_00000006761

 


代谢物信息卡片


InChI=1\C12H8S2\c1-2-3-5-10-7-8-12(14-10)11-6-4-9-13-11\h2,4,6-9H,1H

化学式: C12H8S2 (216.0067408)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C=CC#CC1=CC=C(S1)C2=CC=CS2
InChI: InChI=1S/C12H8S2/c1-2-3-5-10-7-8-12(14-10)11-6-4-9-13-11/h2,4,6-9H,1H2

描述信息

同义名列表

13 个代谢物同义名

InChI=1\C12H8S2\c1-2-3-5-10-7-8-12(14-10)11-6-4-9-13-11\h2,4,6-9H,1H; 2-but-3-en-1-ynyl-5-thiophen-2-yl-thiophene; 2-but-3-en-1-ynyl-5-thiophen-2-ylthiophene; 2-but-3-en-1-ynyl-5-(2-thienyl)thiophene; 2,2-Bithiophene, 5-(3-buten-1-ynyl)-; 5-but-3-en-1-yn-1-yl-2,2-bithiophene; 5-But-3-en-1-ynyl-[2,2]bithiophenyl; 5-(3-Buten-1-ynyl)-2,2-bithiophene; 5-(3-Buten-1-ynyl)-2,2-bithienyl; MEGxp0_001541; CHEBI:2015; 1134-61-8; C08397



数据库引用编号

8 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

  • Lashyn Kiyekbayeva, Nesma M Mohamed, Orazbekov Yerkebulan, Enas I Mohamed, Datkhayev Ubaidilla, Akhtayeva Nursulu, Mamurova Assem, Radhakrishnan Srivedavyasasri, Samir A Ross. Phytochemical constituents and antioxidant activity of Echinops albicaulis. Natural product research. 2018 May; 32(10):1203-1207. doi: 10.1080/14786419.2017.1323213. [PMID: 28475371]
  • Yun Wei, Kai Zhang, Li Yin, Jilin Du, Guoliang Zhang. Isolation of bioactive components from Flaveria bidentis (L.) Kuntze using high-speed counter-current chromatography and time-controlled collection method. Journal of separation science. 2012 Apr; 35(7):869-74. doi: 10.1002/jssc.201101027. [PMID: 22532356]
  • Bárbara Missiam Mezari Guevara Campos, Anabel Torres Cirio, Verónica Mayela Rivas Galindo, Ricardo Salazar Aranda, Noemí Waksman de Torres, Luis Alejandro Pérez-López. Activity against Streptococcus pneumoniae of the essential oil and 5-(3-buten-1-ynyl)-2, 2'-bithienyl isolated from Chrysactinia mexicana roots. Natural product communications. 2011 Jul; 6(7):1035-8. doi: . [PMID: 21834252]
  • Ilaria Marotti, Mauro Marotti, Roberta Piccaglia, Anna Nastri, Silvia Grandi, Giovanni Dinelli. Thiophene occurrence in different Tagetes species: agricultural biomasses as sources of biocidal substances. Journal of the science of food and agriculture. 2010 May; 90(7):1210-7. doi: 10.1002/jsfa.3950. [PMID: 20394003]
  • Nikolas Fokialakis, Weste L A Osbrink, Leonid K Mamonov, Nadejda G Gemejieva, Amelia B Mims, Alexios L Skaltsounis, Alan R Lax, Charles L Cantrell. Antifeedant and toxicity effects of thiophenes from four Echinops species against the Formosan subterranean termite, Coptotermes formosanus. Pest management science. 2006 Sep; 62(9):832-8. doi: 10.1002/ps.1237. [PMID: 16791907]
  • Nikolas Fokialakis, Charles L Cantrell, Stephen O Duke, Alexios L Skaltsounis, David E Wedge. Antifungal activity of thiophenes from Echinops ritro. Journal of agricultural and food chemistry. 2006 Mar; 54(5):1651-5. doi: 10.1021/jf052702j. [PMID: 16506815]
  • Lilla Margl, Andreas Tei, István Gyurján, Michael Wink. GLC and GLC-mS analysis of thiophene derivatives in plants and in in vitro cultures of Tagetes patula L. (Asteraceae). Zeitschrift fur Naturforschung. C, Journal of biosciences. 2002 Jan; 57(1-2):63-71. doi: 10.1515/znc-2002-1-211. [PMID: 11926545]
  • L Margl, W Eisenreich, P Adam, A Bacher, M H Zenk. Biosynthesis of thiophenes in Tagetes patula. Phytochemistry. 2001 Nov; 58(6):875-81. doi: 10.1016/s0031-9422(01)00360-0. [PMID: 11684184]