α-ionone (BioDeep_00000265891)

PANOMIX_OTCML-2023

代谢物信息卡片

(E)-alpha-lonone

化学式: C13H20O (192.151407)
中文名称: α-紫罗酮
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=CCCC(C1C=CC(=O)C)(C)C
InChI: InChI=1S/C13H20O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h6-8,12H,5,9H2,1-4H3/b8-7+

描述信息

D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids

同义名列表

4 个代谢物同义名

alpha-Ionone; α-ionone; (E)-alpha-lonone; -alpha-lonone

数据库引用编号

11 个数据库交叉引用编号

ChEBI: CHEBI:32319
KEGG: C12286
PubChem: 5282108
ChEMBL: CHEMBL472877
KNApSAcK: C00050769
CAS: 31798-12-6
CAS: 6901-97-9
CAS: 127-41-3
MetaboLights: MTBLC32319
PubChem: 14430
NIKKAJI: J183.660I

分类词条

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)

39 个相关的物种来源信息

4442 Camellia sinensis:
3661 Cucurbita maxima: 10.1021/JF00073A014
4138 Leonurus japonicus: 10.3390/MOLECULES18010963
3755 Prunus dulcis: 10.1021/JF60228A025
3039 Euglena gracilis: 10.3389/FBIOE.2021.662655
137129 Swertia japonica: 10.1246/BCSJ.56.3477
87257 Evernia prunastri: 10.1021/JF60201A022
185542 Ilex paraguariensis: 10.1021/JF00025A023
205076 Vachellia rigidula: 10.1021/JF00120A008
41496 Calendula officinalis: 10.1055/S-2006-962683
202634 Crateva religiosa: 10.1021/NP50052A041
483693 Inula racemosa: 10.1016/S0031-9422(00)83760-7
39334 Leea guineensis: 10.1002/1099-1026(200005/06)15:3<182::AID-FFJ888>3.0.CO;2-X
4045 Apium graveolens: 10.1080/10412905.1990.9697808
103745 Chromolaena odorata: 10.1080/10412905.1992.9698069
48386 Perilla frutescens: 10.1016/0031-9422(83)83016-7
4039 Daucus carota: 10.1021/JF60198A031
55611 Artemisia tridentata: 10.1021/JF60210A021
21880 Salvia: 10.1055/S-2007-969187
4442 Camellia sinensis:
3661 Cucurbita maxima: 10.1021/JF00073A014
4138 Leonurus japonicus: 10.3390/MOLECULES18010963
3755 Prunus dulcis: 10.1021/JF60228A025
3039 Euglena gracilis: 10.3389/FBIOE.2021.662655
137129 Swertia japonica: 10.1246/BCSJ.56.3477
87257 Evernia prunastri: 10.1021/JF60201A022
185542 Ilex paraguariensis: 10.1021/JF00025A023
205076 Vachellia rigidula: 10.1021/JF00120A008
41496 Calendula officinalis: 10.1055/S-2006-962683
202634 Crateva religiosa: 10.1021/NP50052A041
483693 Inula racemosa: 10.1016/S0031-9422(00)83760-7
39334 Leea guineensis: 10.1002/1099-1026(200005/06)15:3<182::AID-FFJ888>3.0.CO;2-X
4045 Apium graveolens: 10.1080/10412905.1990.9697808
103745 Chromolaena odorata: 10.1080/10412905.1992.9698069
48386 Perilla frutescens: 10.1016/0031-9422(83)83016-7
4039 Daucus carota: 10.1021/JF60198A031
55611 Artemisia tridentata: 10.1021/JF60210A021
21880 Salvia: 10.1055/S-2007-969187
569774 金线莲: -

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

Md Mahfuzur Rob, Kawsar Hossen, Kaori Ozaki, Toshiaki Teruya, Hisashi Kato-Noguchi. Phytotoxicity and Phytotoxic Substances in Calamus tenuis Roxb. Toxins. 2023 10; 15(10):. doi: 10.3390/toxins15100595. [PMID: 37888626]
Yukihiro Yoshida, Dai Haraguchi, Rie Ukuda-Hosokawa, Tsunaki Andou, Takashi Matsuyama, Tsuguo Kohama, Takashi Eguchi, Satoshi Ohno, Hajime Ono, Ritsuo Nishida. Synthesis and activity of 3-oxo-α-ionone analogs as male attractants for the solanaceous fruit fly, Bactrocera latifrons (Diptera: Tephritidae). Bioscience, biotechnology, and biochemistry. 2021 Nov; 85(12):2360-2367. doi: 10.1093/bbb/zbab166. [PMID: 34601560]
Yanting Zhong, Xiaoying Pan, Ruifeng Wang, Jiuliang Xu, Jingyu Guo, Tingxue Yang, Jianyu Zhao, Faisal Nadeem, Xiaoting Liu, Hongyan Shan, Yanjun Xu, Xuexian Li. ZmCCD10a Encodes a Distinct Type of Carotenoid Cleavage Dioxygenase and Enhances Plant Tolerance to Low Phosphate. Plant physiology. 2020 09; 184(1):374-392. doi: 10.1104/pp.20.00378. [PMID: 32586893]
Mika Murata, Tetsuya Kobayashi, Shigemi Seo. α-Ionone, an Apocarotenoid, Induces Plant Resistance to Western Flower Thrips, Frankliniella occidentalis, Independently of Jasmonic Acid. Molecules (Basel, Switzerland). 2019 Dec; 25(1):. doi: 10.3390/molecules25010017. [PMID: 31861560]
Ilya Lukin, Guido Jach, Isabell Wingartz, Peter Welters, Gerhard Schembecker. Recovery of Natural α-Ionone from Fermentation Broth. Journal of agricultural and food chemistry. 2019 Dec; 67(49):13412-13419. doi: 10.1021/acs.jafc.8b07270. [PMID: 30864443]
Marinella De Leo, Lorenzo Peruzzi, Carlotta Granchi, Tiziano Tuccinardi, Filippo Minutolo, Nunziatina De Tommasi, Alessandra Braca. Constituents of Polygala flavescens ssp. flavescens and Their Activity as Inhibitors of Human Lactate Dehydrogenase. Journal of natural products. 2017 07; 80(7):2077-2087. doi: 10.1021/acs.jnatprod.7b00295. [PMID: 28692289]
Lian Gelis, Nikolina Jovancevic, Sophie Veitinger, Bhubaneswar Mandal, Hans-Dieter Arndt, Eva M Neuhaus, Hanns Hatt. Functional Characterization of the Odorant Receptor 51E2 in Human Melanocytes. The Journal of biological chemistry. 2016 08; 291(34):17772-86. doi: 10.1074/jbc.m116.734517. [PMID: 27226631]
Yao Lu, Zhi-Hong Li, Lin Ma, An-Jun Deng, Feng Wu, Zhi-Hui Zhang, Hai-Lin Qin. [Study on chemical constituents from cultivated Gynura nepalensis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2014 Oct; 39(19):3777-81. doi: . [PMID: 25612439]
Hongyan Sun, Li Guan, Honglin Feng, Jiao Yin, Yazhong Cao, Jinghui Xi, Kebin Li. Functional characterization of chemosensory proteins in the scarab beetle, Holotrichia oblita Faldermann (Coleoptera: Scarabaeida). PloS one. 2014; 9(9):e107059. doi: 10.1371/journal.pone.0107059. [PMID: 25188038]
Hao Cai, Gang Cao, Li Li, Xiao Liu, Xiao-Qing Ma, Si-Cong Tu, Ya-Jing Lou, Kun-Ming Qin, Song-Lin Li, Bao-Chang Cai. Profiling and characterization of volatile components from non-fumigated and sulfur-fumigated Flos Lonicerae Japonicae using comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry coupled with chemical group separation. Molecules (Basel, Switzerland). 2013 Jan; 18(2):1368-82. doi: 10.3390/molecules18021368. [PMID: 23348991]
Kazuya Shimizu, Toshirou Ono, Mitsuo Miyazawa. Highly selective and asymmetric reductive biotransformation of α-ionone by Epicoccum purpurascens. Journal of oleo science. 2013; 62(4):231-4. doi: 10.5650/jos.62.231. [PMID: 23535310]
Jia-xu Wen, De Zhao, Jun Deng. [Influence of processing methods on the chemical composition of the essential oil from Aucklandia lappa]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2012 Sep; 35(9):1397-401. doi: . [PMID: 23451492]
Ufuk Ozgen, Handan Sevindik, Cavit Kazaz, Demet Yigit, Ali Kandemir, Hasan Secen, Ihsan Calis. A new sulfated alpha-ionone glycoside from Sonchus erzincanicus Matthews. Molecules (Basel, Switzerland). 2010 Apr; 15(4):2593-9. doi: 10.3390/molecules15042593. [PMID: 20428066]
Tatsuaki Ishida, Hiroshi Enomoto, Ritsuo Nishida. New attractants for males of the solanaceous fruit fly Bactrocera latifrons. Journal of chemical ecology. 2008 Dec; 34(12):1532-5. doi: 10.1007/s10886-008-9562-8. [PMID: 19018595]
María del Mar Caja, Christina Preston, Michael Kempf, Peter Schreier. Flavor authentication studies of alpha-ionone, beta-ionone, and alpha-ionol from various sources. Journal of agricultural and food chemistry. 2007 Aug; 55(16):6700-4. doi: 10.1021/jf070805r. [PMID: 17630763]
Grant T McQuate, Young Soo Keum, Charmaine D Sylva, Qing X Li, Eric B Jang. Active ingredients in cade oil that synergize attractiveness of alpha-ionol to male Bactrocera latifrons (Diptera: Tephritidae). Journal of economic entomology. 2004 Jun; 97(3):862-70. doi: 10.1603/0022-0493(2004)097[0862:aiicot]2.0.co;2. [PMID: 15279265]
G T McQuate, S L Peck. Enhancement of attraction of alpha-ionol to male Bactrocera latifrons (Diptera: Tephritidae) by addition of a synergist, cade oil. Journal of economic entomology. 2001 Feb; 94(1):39-46. doi: 10.1603/0022-0493-94.1.39. [PMID: 11233131]