Nitramine (BioDeep_00000007918)

   


代谢物信息卡片


(6S,7R)-2-azaspiro[5.5]undecan-7-ol

化学式: C10H19NO (169.14665639999998)
中文名称: (6S,7R)-2-氮杂螺[5.5]-7-十一醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1CCC2(CCCNC2)C(C1)O
InChI: InChI=1S/C10H19NO/c12-9-4-1-2-5-10(9)6-3-7-11-8-10/h9,11-12H,1-8H2/t9-,10+/m1/s1

描述信息

同义名列表

3 个代谢物同义名

(6S,7R)-2-azaspiro[5.5]undecan-7-ol; Nitramine; 2-azaspiro[5.5]undecan-7-ol



数据库引用编号

11 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)

2 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

  • Elizabeth L Rylott, Astrid Lorenz, Neil C Bruce. Biodegradation and biotransformation of explosives. Current opinion in biotechnology. 2011 Jun; 22(3):434-40. doi: 10.1016/j.copbio.2010.10.014. [PMID: 21094036]
  • G Perchet, G Merlina, J-C Revel, M Hafidi, C Richard, E Pinelli. Evaluation of a TiO2 photocatalysis treatment on nitrophenols and nitramines contaminated plant wastewaters by solid-phase extraction coupled with ESI HPLC-MS. Journal of hazardous materials. 2009 Jul; 166(1):284-90. doi: 10.1016/j.jhazmat.2008.11.013. [PMID: 19111394]
  • Sylvie Rocheleau, Bernard Lachance, Roman G Kuperman, Jalal Hawari, Sonia Thiboutot, Guy Ampleman, Geoffrey I Sunahara. Toxicity and uptake of cyclic nitramine explosives in ryegrass Lolium perenne. Environmental pollution (Barking, Essex : 1987). 2008 Nov; 156(1):199-206. doi: 10.1016/j.envpol.2007.12.012. [PMID: 18358578]
  • Steven R Myers, Joseph A Spinnato. Tissue distribution and elimination of N-methyl-N-2,4,6-tetranitroaniline (tetryl) in rats. Archives of toxicology. 2007 Dec; 81(12):841-8. doi: 10.1007/s00204-007-0220-7. [PMID: 17680234]
  • Ghalib K Bardai, Annamaria Halasz, Geoffrey I Sunahara, Sabine Dodard, Philip A Spear, Stephan Grosse, Johnston Hoang, Jalal Hawari. In vitro degradation of hexanitrohexaazaisowurtzitane (CL-20) by cytosolic enzymes of Japanese quail and the rabbit. Environmental toxicology and chemistry. 2006 Dec; 25(12):3221-9. doi: 10.1897/06-068r.1. [PMID: 17220092]
  • Olivier L Collin, Claudia Niegel, Kate E Derhodes, Bruce R McCord, Glen P Jackson. Fast gas chromatography of explosive compounds using a pulsed-discharge electron capture detector. Journal of forensic sciences. 2006 Jul; 51(4):815-8. doi: 10.1111/j.1556-4029.2006.00171.x. [PMID: 16882225]
  • Jong Moon Yoon, Benoit Van Aken, Jerald L Schnoor. Leaching of contaminated leaves following uptake and phytoremediation of RDX, HMX, and TNT by poplar. International journal of phytoremediation. 2006; 8(1):81-94. doi: 10.1080/15226510500507128. [PMID: 16615309]
  • Melissa P Mezzari, Benoit Van Aken, Jong M Yoon, Craig L Just, Jerald L Schnoor. Mathematical modeling of RDX and HMX metabolism in poplar (Populus deltoides x Populus nigra, DN34) tissue culture. International journal of phytoremediation. 2004; 6(4):323-45. doi: 10.1080/16226510490888839. [PMID: 15696705]
  • N Cenas, A Nemeikaite-Ceniene, E Sergediene, H Nivinskas, Z Anusevicius, J Sarlauskas. Quantitative structure-activity relationships in enzymatic single-electron reduction of nitroaromatic explosives: implications for their cytotoxicity. Biochimica et biophysica acta. 2001 Sep; 1528(1):31-8. doi: 10.1016/s0304-4165(01)00169-6. [PMID: 11514095]
  • C A Groom, S Beaudet, A Halasz, L Paquet, J Hawari. Detection of the cyclic nitramine explosives hexahydro-1,3,5-trinitro- 1,3,5-triazine (RDX) and octahydro- 1,3,5,7-tetranitro- 1,3,5,7-tetrazine (HMX) and their degradation products in soil environments. Journal of chromatography. A. 2001 Feb; 909(1):53-60. doi: 10.1016/s0021-9673(00)01043-8. [PMID: 11218141]