5,15-diHPETE (BioDeep_00000607968)
代谢物信息卡片
化学式: C20H32O6 (368.2199)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCCCC(/C=C/C=C\C/C=C\C=C\C(CCCC(=O)O)OO)OO
InChI: InChI=1S/C20H32O6/c1-2-3-9-13-18(25-23)14-10-7-5-4-6-8-11-15-19(26-24)16-12-17-20(21)22/h5-8,10-11,14-15,18-19,23-24H,2-4,9,12-13,16-17H2,1H3,(H,21,22)/b7-5-,8-6-,14-10+,15-11+
描述信息
D009676 - Noxae > D016877 - Oxidants > D010545 - Peroxides
同义名列表
数据库引用编号
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)
0 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。
| 亚细胞结构定位 | 关联基因列表 |
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文献列表
- Alejandro Cruz, Àngels González-Lafont, José M Lluch. Deciphering the Molecular Details of the Lipoxin Formation Mechanism in the 5(S),15(S)-DiHpETE Biosynthetic Pathway Catalyzed by Reticulocyte 15-Lipoxygenase-1.
The journal of physical chemistry. B.
2020 12; 124(50):11406-11418. doi:
10.1021/acs.jpcb.0c09147. [PMID: 33274949] - Abigail R Green, Cody Freedman, Jennyfer Tena, Benjamin E Tourdot, Benjamin Liu, Michael Holinstat, Theodore R Holman. 5 S,15 S-Dihydroperoxyeicosatetraenoic Acid (5,15-diHpETE) as a Lipoxin Intermediate: Reactivity and Kinetics with Human Leukocyte 5-Lipoxygenase, Platelet 12-Lipoxygenase, and Reticulocyte 15-Lipoxygenase-1.
Biochemistry.
2018 12; 57(48):6726-6734. doi:
10.1021/acs.biochem.8b00889. [PMID: 30407793] - Gianguido Coffa, Ann N Imber, Brendan C Maguire, Gurunathan Laxmikanthan, Claus Schneider, Betty J Gaffney, Alan R Brash. On the relationships of substrate orientation, hydrogen abstraction, and product stereochemistry in single and double dioxygenations by soybean lipoxygenase-1 and its Ala542Gly mutant.
The Journal of biological chemistry.
2005 Nov; 280(46):38756-66. doi:
10.1074/jbc.m504870200. [PMID: 16157595] - D E Sok, T S Phi, C H Jung, Y S Chung, J B Kang. Soybean lipoxygenase-catalyzed formation of lipoxin A and lipoxin B isomers from arachidonic acid via 5,15-dihydroperoxyeicosatetraenoic acid.
Biochemical and biophysical research communications.
1988 Jun; 153(2):840-7. doi:
10.1016/s0006-291x(88)81172-0. [PMID: 3132921] - S Yamamoto, N Ueda, C Yokoyama, B J Fitzsimmons, J Rokach, J A Oates, A R Brash. Lipoxin syntheses by arachidonate 12- and 5-lipoxygenases purified from porcine leukocytes.
Advances in experimental medicine and biology.
1988; 229(?):15-26. doi:
10.1007/978-1-4757-0937-7_2. [PMID: 3421157] - B Fitzsimmons, J Rokach. The lipoxins: synthesis and biosynthesis.
Advances in experimental medicine and biology.
1988; 229(?):79-92. doi:
10.1007/978-1-4757-0937-7_7. [PMID: 3421159] - N Ueda, C Yokoyama, S Yamamoto, B J Fitzsimmons, J Rokach, J A Oates, A R Brash. Lipoxin synthesis by arachidonate 12-lipoxygenase purified from porcine leukocytes.
Biochemical and biophysical research communications.
1987 Dec; 149(3):1063-9. doi:
10.1016/0006-291x(87)90516-x. [PMID: 3122743]
