FA 12:2 (BioDeep_00000628825)
Volatile Flavor Compounds
代谢物信息卡片
化学式: C12H20O2 (196.14632200000003)
中文名称: (Z) -4-羟基-6-十二碳烯酸内酯, 顺式-4-羟基-6-十二烯酸内酯
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C#CCCCCCCCCCC(=O)O
InChI: InChI=1S/C12H20O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h1H,3-11H2,(H,13,14)
描述信息
同义名列表
56 个代谢物同义名
(Z)-dihydro-5-(2-octenyl)furan-2(3H)-one; (Z)-4-Hydroxy-6-dodecenoic acid lactone; 5-[(2Z)-oct-2-en-1-yl]oxolan-2-one; FA 12:2; 5-Dodecen-11-olide; 3Z-Dodecen-12-olide; Cucujolide VIII; 3Z-Dodecen-11S-olide; Ferrulactone II; S-Cucujolide II; 3Z-Dodecen-11R-olide; Cucujolide II; 5R-(oct-1Z-enyl)dihydrofuran-2(3H)-one; 5R-(Oct-1Z-enyl)-oxacyclopentan-2-one; Dodec-5Z-en-4R-olide; Buibuilactone; (2E,4E,6S)-4,6-dimethyldeca-2,4-dienoic acid; 4,6S-dimethyl-2E,4E-decadienoic acid; Phialomustin B; (2E,4E,6R)-4,6-dimethyldeca-2,4-dienoic acid; 4,6R-dimethyl-2E,4E-decadienoic acid; (R)-(-)-phialomustin B; cis,cis-dodeca-3,6-dienoic acid; 3Z,6Z-dodecadienoic acid; C12:2n-6,9; 11-dodecynoic acid; 10-dodecynoic acid; 9-dodecynoic acid; 8-dodecynoic acid; 7-dodecynoic acid; 6-dodecynoic acid; 5-dodecynoic acid; 4-dodecynoic acid; 3-dodecynoic acid; 8Z,10E-dodecadienoic acid; C12:2n-2,4; 8E,10E-dodecadienoic acid; 7Z,9E-dodecadienoic acid; C12:2n-3,5; 5E,7E-dodecadienoic acid; C12:2n-5,7; 2Z,8Z-dodecadienoic acid; C12:2n-4,10; 2Z,8E-dodecadienoic acid; 2E,8Z-dodecadienoic acid; 2E,8E-dodecadienoic acid; 2E,6Z-dodecadienoic acid; C12:2n-6,10; 2E,4E-dodecadienoic acid; C12:2n-8,10; 7-(2-cyclopenten-1-yl)heptanoic acid; 7-(2-cyclopentenyl)-heptanoic acid; 7-(cyclopent-2-enyl)heptanoic acid; 2-cyclopentene-1-heptanoic acid; Aleprylic acid; (Z)-4-Hydroxy-6-dodecenoic acid lactone
数据库引用编号
86 个数据库交叉引用编号
- ChEBI: CHEBI:172053
- ChEBI: CHEBI:195916
- ChEBI: CHEBI:195914
- ChEBI: CHEBI:185643
- ChEBI: CHEBI:195913
- ChEBI: CHEBI:37210
- ChEBI: CHEBI:195921
- ChEBI: CHEBI:195922
- ChEBI: CHEBI:165490
- ChEBI: CHEBI:195917
- ChEBI: CHEBI:195918
- ChEBI: CHEBI:195919
- ChEBI: CHEBI:195920
- ChEBI: CHEBI:165469
- ChEBI: CHEBI:165464
- ChEBI: CHEBI:195926
- ChEBI: CHEBI:191878
- ChEBI: CHEBI:184267
- ChEBI: CHEBI:187784
- ChEBI: CHEBI:195925
- ChEBI: CHEBI:195923
- ChEBI: CHEBI:195924
- ChEBI: CHEBI:185954
- ChEBI: CHEBI:187643
- PubChem: 5352428
- PubChem: 5365576
- PubChem: 11019790
- PubChem: 10867249
- PubChem: 56936043
- PubChem: 121012351
- PubChem: 11966237
- PubChem: 152196
- PubChem: 5312613
- PubChem: 5312612
- PubChem: 5312611
- PubChem: 5312610
- PubChem: 5312609
- PubChem: 5312608
- PubChem: 5312607
- PubChem: 5312606
- PubChem: 5312391
- PubChem: 5312390
- PubChem: 5312389
- PubChem: 5312388
- PubChem: 5312387
- PubChem: 5312386
- PubChem: 5312385
- PubChem: 5312384
- PubChem: 5282853
- LipidMAPS: LMFA07040067
- LipidMAPS: LMFA07040041
- LipidMAPS: LMFA07040035
- LipidMAPS: LMFA07040034
- LipidMAPS: LMFA07040033
- LipidMAPS: LMFA07040029
- LipidMAPS: LMFA01031270
- LipidMAPS: LMFA01031269
- LipidMAPS: LMFA01030769
- LipidMAPS: LMFA01030474
- LipidMAPS: LMFA01030473
- LipidMAPS: LMFA01030472
- LipidMAPS: LMFA01030471
- LipidMAPS: LMFA01030470
- LipidMAPS: LMFA01030469
- LipidMAPS: LMFA01030468
- LipidMAPS: LMFA01030467
- LipidMAPS: LMFA01030466
- LipidMAPS: LMFA01030239
- LipidMAPS: LMFA01030238
- LipidMAPS: LMFA01030237
- LipidMAPS: LMFA01030236
- LipidMAPS: LMFA01030235
- LipidMAPS: LMFA01030234
- LipidMAPS: LMFA01030233
- LipidMAPS: LMFA01030232
- LipidMAPS: LMFA01030231
- LipidMAPS: LMFA01030230
- LipidMAPS: LMFA01030189
- CAS: 18679-18-0
- CAS: 87371-99-1
- CAS: 16900-60-0
- CAS: 19307-25-6
- CAS: 18545-07-8
- CAS: 676-17-5
- CAS: 55182-75-7
- CAS: 2348-91-6
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。
文献列表
- Shou-Jie Li, Xuan Zhang, Xiang-Hua Wang, Chang-Qi Zhao. Novel natural compounds from endophytic fungi with anticancer activity.
European journal of medicinal chemistry.
2018 Aug; 156(?):316-343. doi:
10.1016/j.ejmech.2018.07.015
. [PMID: 30015071] - Jeroen S Dickschat, Irene Wagner-Döbler, Stefan Schulz. The chafer pheromone buibuilactone and ant pyrazines are also produced by marine bacteria.
Journal of chemical ecology.
2005 Apr; 31(4):925-47. doi:
10.1007/s10886-005-3553-9
. [PMID: 16124260] - C Sabourault, G de Sousa, M Amichot, A Cuany, R Rahmani, J P Salaün, J B Bergé, J P Girard, M Lafaurie. Tissue-specific induction and inactivation of cytochrome P450 catalysing lauric acid hydroxylation in the sea bass, Dicentrarchus labrax.
Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.
1999 Feb; 122(2):253-60. doi:
10.1016/s0305-0491(99)00006-1
. [PMID: 10327614] - N Tijet, C Helvig, F Pinot, R Le Bouquin, A Lesot, F Durst, J P Salaün, I Benveniste. Functional expression in yeast and characterization of a clofibrate-inducible plant cytochrome P-450 (CYP94A1) involved in cutin monomers synthesis.
The Biochemical journal.
1998 Jun; 332 ( Pt 2)(?):583-9. doi:
10.1042/bj3320583
. [PMID: 9601090] - J P Salaün, A Simon, F Durst, N O Reich, P R Ortiz de Montellano. Differential inactivation of plant lauric acid omega- and in-chain-hydroxylases by terminally unsaturated fatty acids.
Archives of biochemistry and biophysics.
1988 Feb; 260(2):540-5. doi:
10.1016/0003-9861(88)90479-1
. [PMID: 3341756] - A J Blotcky, G T Hansen, N Borkar, A Ebrahim, E P Rack. Simultaneous determination of selenite and trimethylselenonium ions in urine by anion exchange chromatography and molecular neutron activation analysis.
Analytical chemistry.
1987 Sep; 59(17):2063-6. doi:
10.1021/ac00144a012
. [PMID: 3674425] - N O Reich, P R Ortiz de Montellano. Dissociation of increased lauric acid omega-hydroxylase activity from the antilipidemic action of clofibrate.
Biochemical pharmacology.
1986 Apr; 35(8):1227-33. doi:
10.1016/0006-2952(86)90264-9
. [PMID: 3964299] - S Nakazawa, H Sato, K Niino, S Nakazawa, Y Hirama, A Narita, H Chikaoka, S Oka. [Fundamental and clinical studies on CS--1170 in pediatric field (author's transl)].
The Japanese journal of antibiotics.
1979 Feb; 32(2):227-37. doi:
NULL
. [PMID: 439394]