13-Apo-beta-carotenone (BioDeep_00000013611)
Volatile Flavor Compounds
代谢物信息卡片
化学式: C18H26O (258.1983546)
中文名称: 13载脂蛋白β-胡萝卜素
谱图信息:
最多检出来源 Viridiplantae(plant) 0.06%
分子结构信息
SMILES: C/C(=C\C=C\C(=O)C)/C=C/C1=C(C)CCCC1(C)C
InChI: InChI=1S/C18H26O/c1-14(8-6-10-16(3)19)11-12-17-15(2)9-7-13-18(17,4)5/h6,8,10-12H,7,9,13H2,1-5H3/b10-6+,12-11+,14-8+
描述信息
D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids
同义名列表
数据库引用编号
9 个数据库交叉引用编号
- ChEBI: CHEBI:53175
- KEGG: C20696
- PubChem: 5363697
- PubChem: 196568
- MetaCyc: CPD-13369
- CAS: 17974-57-1
- PMhub: MS000028109
- PubChem: 172232416
- RefMet: 13-apo-beta-Carotenone
分类词条
相关代谢途径
Reactome(0)
代谢反应
7 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- carotenoid cleavage:
β-carotene + O2 ⟶ β-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial
- carotenoid cleavage:
all-trans-β-carotene + O2 ⟶ β-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(5)
- carotenoid cleavage:
β-carotene + O2 ⟶ β-ionone + all-trans-10'-apo-β-carotenal
- carotenoid cleavage:
β-carotene + O2 ⟶ β-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial
- carotenoid cleavage:
β-carotene + O2 ⟶ β-ionone + all-trans-10'-apo-β-carotenal
- carotenoid cleavage:
β-carotene + O2 ⟶ β-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial
- carotenoid cleavage:
β-carotene + O2 ⟶ β-ionone + all-trans-10'-apo-β-carotenal
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
- Boluwatiwi O Durojaye, Kenneth M Riedl, Robert W Curley, Earl H Harrison. Uptake and metabolism of β-apo-8'-carotenal, β-apo-10'-carotenal, and β-apo-13-carotenone in Caco-2 cells.
Journal of lipid research.
2019 06; 60(6):1121-1135. doi:
10.1194/jlr.m093161
. [PMID: 30846527] - Rachel E Kopec, Catherine Caris-Veyrat, Marion Nowicki, Beatrice Gleize, Michel Carail, Patrick Borel. Production of asymmetric oxidative metabolites of [13C]-β-carotene during digestion in the gastrointestinal lumen of healthy men.
The American journal of clinical nutrition.
2018 10; 108(4):803-813. doi:
10.1093/ajcn/nqy183
. [PMID: 30256893] - Jessica L Cooperstone, Janet A Novotny, Ken M Riedl, Morgan J Cichon, David M Francis, Robert W Curley, Steven J Schwartz, Earl H Harrison. Limited appearance of apocarotenoids is observed in plasma after consumption of tomato juices: a randomized human clinical trial.
The American journal of clinical nutrition.
2018 10; 108(4):784-792. doi:
10.1093/ajcn/nqy177
. [PMID: 30239552] - Katharina Wagner, Katrin Krause, Anja David, Marco Kai, Elke-Martina Jung, Dominik Sammer, Olaf Kniemeyer, Wilhelm Boland, Erika Kothe. Influence of zygomycete-derived D'orenone on IAA signalling in Tricholoma-spruce ectomycorrhiza.
Environmental microbiology.
2016 09; 18(8):2470-80. doi:
10.1111/1462-2920.13160
. [PMID: 26636983] - Abdulkerim Eroglu, Damian P Hruszkewycz, Carlo dela Sena, Sureshbabu Narayanasamy, Ken M Riedl, Rachel E Kopec, Steven J Schwartz, Robert W Curley, Earl H Harrison. Naturally occurring eccentric cleavage products of provitamin A β-carotene function as antagonists of retinoic acid receptors.
The Journal of biological chemistry.
2012 May; 287(19):15886-95. doi:
10.1074/jbc.m111.325142
. [PMID: 22418437] - Rebekah S Marsh, Yan Yan, Vanessa M Reed, Damian Hruszkewycz, Robert W Curley, Earl H Harrison. {beta}-Apocarotenoids do not significantly activate retinoic acid receptors {alpha} or {beta}.
Experimental biology and medicine (Maywood, N.J.).
2010 Mar; 235(3):342-8. doi:
10.1258/ebm.2009.009202
. [PMID: 20404052] - Adrian Alder, Iris Holdermann, Peter Beyer, Salim Al-Babili. Carotenoid oxygenases involved in plant branching catalyse a highly specific conserved apocarotenoid cleavage reaction.
The Biochemical journal.
2008 Dec; 416(2):289-96. doi:
10.1042/bj20080568
. [PMID: 18637791] - . .
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. doi:
. [PMID: 15342640]