Prenol (BioDeep_00000408265)
Main id: BioDeep_00000629759
PANOMIX_OTCML-2023 natural product BioNovoGene_Lab2019
代谢物信息卡片
化学式: C5H10O (86.0732)
中文名称: 3-甲基-2-丁烯-1-醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C/C(C)=C\CO
InChI: InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3
描述信息
3-Methyl-2-buten-1-ol is an endogenous metabolite.
3-Methyl-2-buten-1-ol is an endogenous metabolite.
同义名列表
30 个代谢物同义名
4-01-00-02129 (Beilstein Handbook Reference); InChI=1\C5H10O\c1-5(2)3-4-6\h3,6H,4H2,1-2H; .gamma.,.gamma.-Dimethylallyl alcohol; 3-Methyl-2-butenyl alcohol; 3,3-Dimethylallyl alcohol; 2-Buten-1-ol, 3-methyl-; 3-Methylcrotyl alcohol; Dimethylallyl alcohol; 3-METHYL-2-BUTEN-1-OL; 3-Methylbut-2-en-1-ol; 3-Methyl-2-butenol; EINECS 209-141-4; W364703_ALDRICH; 162353_ALDRICH; Butenol methyl; Prenyl alcohol; FEMA No. 3647; ZINC00897129; 66093_FLUKA; BRN 1633479; 39121_FLUKA; CHEBI:16019; 135146-66-6; NSC 158709; NSC158709; 556-82-1; Prenol; C01390; Prenol; 3-Methyl-2-buten-1-OL
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:16019
- KEGG: C01390
- PubChem: 11173
- ChEMBL: CHEMBL3184952
- CAS: 556-82-1
- MoNA: MoNA002174
- MoNA: MoNA002173
- MoNA: MoNA002172
- PubChem: 4583
- LipidMAPS: LMFA05000106
- PDB-CCD: P1W
- 3DMET: B00282
- NIKKAJI: J11.528B
- medchemexpress: HY-W013035
- LOTUS: LTS0257971
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-383
- KNApSAcK: 16019
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)
74 个相关的物种来源信息
- 94326 - Alpinia: LTS0257971
- 199623 - Alpinia officinarum: 10.1021/JF025529P
- 199623 - Alpinia officinarum: LTS0257971
- 40948 - Angelica: LTS0257971
- 85712 - Angelica gigas: 10.1080/14786410601129598
- 85712 - Angelica gigas: LTS0257971
- 13336 - Annona: LTS0257971
- 49857 - Annona montana: 10.1080/10412905.2002.9699846
- 49857 - Annona montana: LTS0257971
- 22140 - Annonaceae: LTS0257971
- 4037 - Apiaceae: LTS0257971
- 4056 - Apocynaceae: LTS0257971
- 137670 - Bistorta: LTS0257971
- 1548133 - Bistorta manshuriensis: 10.1002/CBDV.201100326
- 1548133 - Bistorta manshuriensis: LTS0257971
- 4849 - Blakeslea: LTS0257971
- 4850 - Blakeslea trispora: 10.1016/0031-9422(80)83069-X
- 4850 - Blakeslea trispora: LTS0257971
- 3593 - Cactaceae: LTS0257971
- 13392 - Cananga: LTS0257971
- 13393 - Cananga odorata: 10.1021/JF00069A028
- 13393 - Cananga odorata: LTS0257971
- 301453 - Capparaceae: LTS0257971
- 13394 - Capparis: LTS0257971
- 65558 - Capparis spinosa: 10.1080/10575630290034302
- 65558 - Capparis spinosa: LTS0257971
- 260594 - Cedronella: LTS0257971
- 260595 - Cedronella canariensis: 10.1016/0031-9422(95)00241-X
- 260595 - Cedronella canariensis: LTS0257971
- 101094 - Choanephoraceae: LTS0257971
- 13442 - Coffea: LTS0257971
- 13443 - Coffea arabica: 10.1021/JF60160A010
- 13443 - Coffea arabica: LTS0257971
- 3781 - Crassulaceae: LTS0257971
- 2759 - Eukaryota: LTS0257971
- 48037 - Foeniculum: LTS0257971
- 48038 - Foeniculum vulgare: 10.1248/CPB.46.1643
- 4751 - Fungi: LTS0257971
- 4136 - Lamiaceae: LTS0257971
- 4447 - Liliopsida: LTS0257971
- 3398 - Magnoliopsida: LTS0257971
- 2212703 - Mucoromycetes: LTS0257971
- 1913637 - Mucoromycota: LTS0257971
- 106975 - Opuntia: LTS0257971
- 371859 - Opuntia ficus-indica: 10.1021/JF60218A053
- 371859 - Opuntia ficus-indica: LTS0257971
- 4724 - Pandanaceae: LTS0257971
- 4725 - Pandanus: LTS0257971
- 4726 - Pandanus tectorius: 10.1016/S0031-9422(96)00386-X
- 4726 - Pandanus tectorius: LTS0257971
- 3684 - Passiflora: LTS0257971
- 78168 - Passiflora edulis: 10.1016/0031-9422(95)00814-4
- 78168 - Passiflora edulis: LTS0257971
- 3683 - Passifloraceae: LTS0257971
- 52847 - Plumeria: LTS0257971
- 62097 - Plumeria rubra: 10.1002/FFJ.2730070108
- 62097 - Plumeria rubra: LTS0257971
- 3615 - Polygonaceae: LTS0257971
- 202994 - Rhodiola: LTS0257971
- 242839 - Rhodiola crenulata: 10.1515/ZNC-2003-3-402
- 242839 - Rhodiola crenulata: LTS0257971
- 24966 - Rubiaceae: LTS0257971
- 23513 - Rutaceae: LTS0257971
- 35493 - Streptophyta: LTS0257971
- 58023 - Tracheophyta: LTS0257971
- 33090 - Viridiplantae: LTS0257971
- 67937 - Zanthoxylum: LTS0257971
- 354530 - Zanthoxylum schinifolium: 10.1021/JF0728101
- 354530 - Zanthoxylum schinifolium: LTS0257971
- 4642 - Zingiberaceae: LTS0257971
- 33090 - 矮地茶: -
- 33090 - 羌活: -
- 33090 - 蛇床子: -
- 33090 - 麻黄: -
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
- Xin Jin, Michael Ackah, Lei Wang, Frank Kwarteng Amoako, Yisu Shi, Lionnelle Gyllye Essoh, Jianbin Li, Qiaonan Zhang, Haonan Li, Weiguo Zhao. Magnesium Nutrient Application Induces Metabolomics and Physiological Responses in Mulberry (Morus alba) Plants.
International journal of molecular sciences.
2023 Jun; 24(11):. doi:
10.3390/ijms24119650
. [PMID: 37298601] - Ryan P Sweeney, Todd L Lowary. A Route to Polyprenol Pyrophosphate-Based Probes of O-Polysaccharide Biosynthesis in Klebsiella pneumoniae O2a.
Organic letters.
2019 02; 21(4):1050-1053. doi:
10.1021/acs.orglett.8b04093
. [PMID: 30681873] - Ran Tao, Chengzhang Wang, Changwei Zhang, WenJun Li, Hao Zhou, Hongxia Chen, Jianzhong Ye. Characterization, Cytotoxicity, and Genotoxicity of TiO2 and Folate-Coupled Chitosan Nanoparticles Loading Polyprenol-Based Nanoemulsion.
Biological trace element research.
2018 Jul; 184(1):60-74. doi:
10.1007/s12011-017-1184-y
. [PMID: 28993980] - Hiroshi Sagami, Ewa Swiezewska, Yoshihiro Shidoji. The history and recent advances in research of polyprenol and its derivatives.
Bioscience, biotechnology, and biochemistry.
2018 Jun; 82(6):947-955. doi:
10.1080/09168451.2017.1411775
. [PMID: 29297247] - Jerry Eichler, Barbara Imperiali. Stereochemical Divergence of Polyprenol Phosphate Glycosyltransferases.
Trends in biochemical sciences.
2018 01; 43(1):10-17. doi:
10.1016/j.tibs.2017.10.008
. [PMID: 29183665] - Miroslav Lísa, Michal Holčapek. UHPSFC/ESI-MS Analysis of Lipids.
Methods in molecular biology (Clifton, N.J.).
2018; 1730(?):73-82. doi:
10.1007/978-1-4939-7592-1_5
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Pharmacological research.
2016 11; 113(Pt B):760-770. doi:
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Journal of lipid research.
2016 06; 57(6):1051-8. doi:
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Journal of separation science.
2016 Feb; 39(3):525-7. doi:
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BioMed research international.
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Journal of chromatography. A.
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Lipids.
2015 04; 50(4):359-70. doi:
10.1007/s11745-015-3998-8
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Molecules (Basel, Switzerland).
2013 Feb; 18(2):2166-82. doi:
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Bioorganic & medicinal chemistry.
2012 Sep; 20(18):5518-26. doi:
10.1016/j.bmc.2012.07.025
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Fitoterapia.
2012 Jul; 83(5):831-7. doi:
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Journal of experimental botany.
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PLoS neglected tropical diseases.
2011 Dec; 5(12):e1451. doi:
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Fitoterapia.
2011 Sep; 82(6):834-40. doi:
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BMC plant biology.
2011 May; 11(?):87. doi:
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Drug development and industrial pharmacy.
2011 May; 37(5):583-96. doi:
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. [PMID: 21469947] - Ewa Ciepichal, Malgorzata Jemiola-Rzeminska, Jozefina Hertel, Ewa Swiezewska, Kazimierz Strzalka. Configuration of polyisoprenoids affects the permeability and thermotropic properties of phospholipid/polyisoprenoid model membranes.
Chemistry and physics of lipids.
2011 May; 164(4):300-6. doi:
10.1016/j.chemphyslip.2011.03.004
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Microbial cell factories.
2011 Jan; 10(?):4. doi:
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Frontiers in physiology.
2011; 2(?):45. doi:
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Plant physiology.
2010 Nov; 154(3):1116-27. doi:
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Journal of agricultural and food chemistry.
2009 Oct; 57(20):9676-81. doi:
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. [PMID: 19803519] - Masayoshi Muramatsu, Chikara Ohto, Shusei Obata, Eiji Sakuradani, Sakayu Shimizu. Various oils and detergents enhance the microbial production of farnesol and related prenyl alcohols.
Journal of bioscience and bioengineering.
2008 Sep; 106(3):263-7. doi:
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. [PMID: 18930003] - Geetu Singh, Prasoon Gupta, Preeti Rawat, Anju Puri, Gitika Bhatia, Rakesh Maurya. Antidyslipidemic activity of polyprenol from Coccinia grandis in high-fat diet-fed hamster model.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2007 Dec; 14(12):792-8. doi:
10.1016/j.phymed.2007.06.008
. [PMID: 17689941] - Ewa Ciepichal, Jacek Wojcik, Tomasz Bienkowski, Magdalena Kania, Malgorzata Swist, Witold Danikiewicz, Andrzej Marczewski, Jozefina Hertel, Zdzislaw Matysiak, Ewa Swiezewska, Tadeusz Chojnacki. Alloprenols: novel alpha-trans-polyprenols of Allophylus caudatus.
Chemistry and physics of lipids.
2007 Jun; 147(2):103-12. doi:
10.1016/j.chemphyslip.2007.04.002
. [PMID: 17507003] - Francesco Epifano, Salvatore Genovese, Luigi Menghini, Massimo Curini. Chemistry and pharmacology of oxyprenylated secondary plant metabolites.
Phytochemistry.
2007 Apr; 68(7):939-53. doi:
10.1016/j.phytochem.2007.01.019
. [PMID: 17343885] - Teresa A Garrett, Ziqiang Guan, Christian R H Raetz. Analysis of ubiquinones, dolichols, and dolichol diphosphate-oligosaccharides by liquid chromatography-electrospray ionization-mass spectrometry.
Methods in enzymology.
2007; 432(?):117-43. doi:
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. [PMID: 17954215] - Andrzej Marczewski, Ewa Ciepichal, Le Xuan Canh, Tran The Bach, Ewa Swiezewska, Tadeusz Chojnacki. The search for polyprenols in dendroflora of Vietnam.
Acta biochimica Polonica.
2007; 54(4):727-32. doi:
10.18388/abp.2007_3142
. [PMID: 18066396] - Frank Röck, Sven Mueller, Udo Weimar, Hans-Georg Rammensee, Peter Overath. Comparative analysis of volatile constituents from mice and their urine.
Journal of chemical ecology.
2006 Jun; 32(6):1333-46. doi:
10.1007/s10886-006-9091-2
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Current medicinal chemistry.
2006; 13(2):199-222. doi:
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Journal of lipid research.
2005 Oct; 46(10):2295-8. doi:
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Biochemical and biophysical research communications.
2005 Jun; 331(2):379-83. doi:
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Journal of lipid research.
2005 May; 46(5):839-61. doi:
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Acta biochimica Polonica.
2005; 52(1):233-41. doi:
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2005; 52(1):243-53. doi:
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Eukaryotic cell.
2004 Apr; 3(2):255-63. doi:
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Phytochemistry.
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Zeitschrift fur Naturforschung. C, Journal of biosciences.
2003 Mar; 58(3-4):161-4. doi:
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Journal of cellular biochemistry.
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