Crepenynic acid (BioDeep_00000006456)
Main id: BioDeep_00000408616
natural product
代谢物信息卡片
化学式: C18H30O2 (278.2246)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(C
InChI: InChI=1S/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-5,8,11-17H2,1H3,(H,19,20)/b10-9-
数据库引用编号
15 个数据库交叉引用编号
- ChEBI: CHEBI:16423
- KEGG: C07289
- PubChem: 5281024
- Metlin: METLIN74332
- Metlin: METLIN35331
- KNApSAcK: C00001278
- CAS: 2277-31-8
- PMhub: MS000019501
- ChEBI: CHEBI:14030
- PubChem: 9498
- LipidMAPS: LMFA01030742
- 3DMET: B01085
- NIKKAJI: J13.791J
- KNApSAcK: 14030
- LOTUS: LTS0052336
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)
25 个相关的物种来源信息
- 162640 - Afzelia: LTS0052336
- 162644 - Afzelia quanzensis: 10.1016/0730-725X(94)92542-9
- 162644 - Afzelia quanzensis: LTS0052336
- 4210 - Asteraceae: LTS0052336
- 13422 - Chrysanthemum: LTS0052336
- 147003 - Chrysanthemum zawadskii: 10.1007/S11745-003-1498-6
- 147003 - Chrysanthemum zawadskii: LTS0052336
- 13464 - Crepis: LTS0052336
- 268017 - Crepis foetida:
- 268017 - Crepis foetida: 10.1007/BF02530929
- 268017 - Crepis foetida: 10.1093/JXB/ERM005
- 268017 - Crepis foetida: LTS0052336
- 2759 - Eukaryota: LTS0052336
- 3803 - Fabaceae: LTS0052336
- 25227 - Ixora: LTS0052336
- 591727 - Ixora chinensis: 10.1016/0031-9422(90)85452-L
- 591727 - Ixora chinensis: LTS0052336
- 1231669 - Leiocarpa: LTS0052336
- 2775374 - Leiocarpa brevicompta: 10.1007/BF02534700
- 2775374 - Leiocarpa brevicompta: LTS0052336
- 3398 - Magnoliopsida: LTS0052336
- 24966 - Rubiaceae: LTS0052336
- 35493 - Streptophyta: LTS0052336
- 58023 - Tracheophyta: LTS0052336
- 33090 - Viridiplantae: LTS0052336
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
- Tao Feng, Ya Yang, Lucas Busta, Edgar B Cahoon, Hengchang Wang, Shiyou Lü. FAD2 Gene Radiation and Positive Selection Contributed to Polyacetylene Metabolism Evolution in Campanulids.
Plant physiology.
2019 10; 181(2):714-728. doi:
10.1104/pp.19.00800
. [PMID: 31420445] - Lucas Busta, Won Cheol Yim, Evan William LaBrant, Peng Wang, Lindsey Grimes, Kiah Malyszka, John C Cushman, Patricia Santos, Dylan K Kosma, Edgar B Cahoon. Identification of Genes Encoding Enzymes Catalyzing the Early Steps of Carrot Polyacetylene Biosynthesis.
Plant physiology.
2018 12; 178(4):1507-1521. doi:
10.1104/pp.18.01195
. [PMID: 30333150] - Jeong-Won Nam, T Joseph Kappock. Cloning and transcriptional analysis of Crepis alpina fatty acid desaturases affecting the biosynthesis of crepenynic acid.
Journal of experimental botany.
2007; 58(6):1421-32. doi:
10.1093/jxb/erm005
. [PMID: 17329262] - Nanzad Tsevegsuren, Kenshiro Fujimoto, William W Christie, Yasushi Endo. Occurrence of a novel cis,cis,cis-octadeca-3,9,12-trienoic (Z,Z,Z-octadeca-3,9,12-trienoic) acid in Chrysanthemum (tanacetum) zawadskii herb. (Compositae) seed oil.
Lipids.
2003 May; 38(5):573-8. doi:
10.1007/s11745-003-1498-6
. [PMID: 12880115] - M Lee, M Lenman, A Banaś, M Bafor, S Singh, M Schweizer, R Nilsson, C Liljenberg, A Dahlqvist, P O Gummeson, S Sjödahl, A Green, S Stymne. Identification of non-heme diiron proteins that catalyze triple bond and epoxy group formation.
Science (New York, N.Y.).
1998 May; 280(5365):915-8. doi:
10.1126/science.280.5365.915
. [PMID: 9572738] - W F Nieuwenhuizen, A Van der Kerk-Van Hoof, J H van Lenthe, R C Van Schaik, K Versluis, G A Veldink, J F Vliegenthart. Lipoxygenase is irreversibly inactivated by the hydroperoxides formed from the enynoic analogues of linoleic acid.
Biochemistry.
1997 Apr; 36(15):4480-8. doi:
10.1021/bi962956l
. [PMID: 9109655] - K D Croft, L J Beilin, G L Ford. Differential inhibition of thromboxane B2 and leukotriene B4 biosynthesis by two naturally occurring acetylenic fatty acids.
Biochimica et biophysica acta.
1987 Oct; 921(3):621-4. doi:
10.1016/0005-2760(87)90091-9
. [PMID: 2822134]