Geranylacetone (BioDeep_00000418808)

Main id: BioDeep_00000019377

 

natural product PANOMIX_OTCML-2023


代谢物信息卡片


6,10-Dimethyl-5,9-undecadien-2-one

化学式: C13H22O (194.1670562)
中文名称: 6,10-二甲基-5,9-十一双烯-2-酮, 香叶基丙酮
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=CCCC(=CCCC(=O)C)C)C
InChI: InChI=1/C13H22O/c1-11(2)7-5-8-12(3)9-6-10-13(4)14/h7,9H,5-6,8,10H2,1-4H3/b12-9+

描述信息

同义名列表

3 个代谢物同义名

6,10-Dimethyl-5,9-undecadien-2-one; Geranylacetone; Geranyl acetone



数据库引用编号

7 个数据库交叉引用编号

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)

131 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

  • Hee Ju Yoo, Mi-Young Chung, Hyun-Ah Lee, Soo-Bin Lee, Silvana Grandillo, James J Giovannoni, Je Min Lee. Natural overexpression of CAROTENOID CLEAVAGE DIOXYGENASE 4 in tomato alters carotenoid flux. Plant physiology. 2023 Jan; ?(?):. doi: 10.1093/plphys/kiad049. [PMID: 36715630]
  • Matilda Lindmark, Suresh Ganji, Erika A Wallin, Fredrik Schlyter, C Rikard Unelius. Semiochemicals produced by fungal bark beetle symbiont Endoconidiophora rufipennis and the discovery of an anti-attractant for Ips typographus. PloS one. 2023; 18(4):e0283906. doi: 10.1371/journal.pone.0283906. [PMID: 37023040]
  • Anna Wróblewska-Kurdyk, Katarzyna Dancewicz, Anna Gliszczyńska, Beata Gabryś. Antifeedant Potential of Geranylacetone and Nerylacetone and Their Epoxy-Derivatives against Myzus persicae (Sulz.). Molecules (Basel, Switzerland). 2022 Dec; 27(24):. doi: 10.3390/molecules27248871. [PMID: 36558003]
  • 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]
  • Alenka Žunič-Kosi, Nataša Stritih-Peljhan, Yunfan Zou, J Steven McElfresh, Jocelyn G Millar. A male-produced aggregation-sex pheromone of the beetle Arhopalus rusticus (Coleoptera: Cerambycidae, Spondylinae) may be useful in managing this invasive species. Scientific reports. 2019 12; 9(1):19570. doi: 10.1038/s41598-019-56094-7. [PMID: 31863031]
  • Saad Bello Saad, Mohammed Auwal Ibrahim, Isa Danladi Jatau, Mohammed Nasir Shuaibu. Trypanostatic activity of geranylacetone: Mitigation of Trypanosoma congolense-associated pathological pertubations and insight into the mechanism of anaemia amelioration using in vitro and in silico models. Experimental parasitology. 2019 Jun; 201(?):49-56. doi: 10.1016/j.exppara.2019.04.011. [PMID: 31029700]
  • Sean T Halloran, R Maxwell Collignon, J Steven McElfresh, Jocelyn G Millar. Fuscumol and Geranylacetone as Pheromone Components of Californian Longhorn Beetles (Coleoptera: Cerambycidae) in the Subfamily Spondylidinae. Environmental entomology. 2018 10; 47(5):1300-1305. doi: 10.1093/ee/nvy101. [PMID: 29986003]
  • Shinsuke Marumoto, Yoshiharu Okuno, Mitsuo Miyazawa. Inhibition of β-Secretase Activity by Monoterpenes, Sesquiterpenes, and C13 Norisoprenoids. Journal of oleo science. 2017 Aug; 66(8):851-855. doi: 10.5650/jos.ess16188. [PMID: 28381772]
  • Igor A Schepetkin, Svetlana V Kushnarenko, Gulmira Özek, Liliya N Kirpotina, Pritam Sinharoy, Gulzhakhan A Utegenova, Karime T Abidkulova, Temel Özek, Kemal Hüsnü Can Başer, Anastasia R Kovrizhina, Andrei I Khlebnikov, Derek S Damron, Mark T Quinn. Modulation of Human Neutrophil Responses by the Essential Oils from Ferula akitschkensis and Their Constituents. Journal of agricultural and food chemistry. 2016 Sep; 64(38):7156-70. doi: 10.1021/acs.jafc.6b03205. [PMID: 27586050]
  • S Mabrouk, A Elaissi, H Ben Jannet, F Harzallah-Skhiri. Chemical composition of essential oils from leaves, stems, flower heads and roots of Conyza bonariensis L. from Tunisia. Natural product research. 2011 Jan; 25(1):77-84. doi: 10.1080/14786419.2010.513685. [PMID: 21240765]
  • Rafal Piskorski, Silvia Dorn. Early-season headspace volatiles from apple and their effect on the apple blossom weevil Anthonomus pomorum. Chemistry & biodiversity. 2010 Sep; 7(9):2254-60. doi: 10.1002/cbdv.201000221. [PMID: 20860027]
  • Ameur Elaissi, Hanène Medini, Mohamed Larbi Khouja, Monique Simmonds, Fréderic Lynene, Farhat Farhat, Rachid Chemli, Fethia Harzallah-Skhiri. Variation in volatile leaf oils of eleven eucalyptus species harvested from korbous arboreta (Tunisia). Chemistry & biodiversity. 2010 Jul; 7(7):1841-54. doi: 10.1002/cbdv.200900381. [PMID: 20658674]
  • Hongyan Gao, Hongliang Zhu, Yi Shao, Anjun Chen, Chengwen Lu, Benzhong Zhu, Yunbo Luo. Lycopene accumulation affects the biosynthesis of some carotenoid-related volatiles independent of ethylene in tomato. Journal of integrative plant biology. 2008 Aug; 50(8):991-6. doi: 10.1111/j.1744-7909.2008.00685.x. [PMID: 18713349]
  • Andrew J Simkin, Steven H Schwartz, Michele Auldridge, Mark G Taylor, Harry J Klee. The tomato carotenoid cleavage dioxygenase 1 genes contribute to the formation of the flavor volatiles beta-ionone, pseudoionone, and geranylacetone. The Plant journal : for cell and molecular biology. 2004 Dec; 40(6):882-92. doi: 10.1111/j.1365-313x.2004.02263.x. [PMID: 15584954]