Methylisoeugenol (BioDeep_00000008111)
Secondary id: BioDeep_00000396202, BioDeep_00000862365, BioDeep_00000872462
human metabolite PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C11H14O2 (178.09937440000002)
中文名称: 顺式-甲基异丁香油酚, 异丁香酚甲醚, 反式甲基异丁香酚
谱图信息:
最多检出来源 Viridiplantae(plant) 0.09%
Last reviewed on 2024-08-13.
Cite this Page
Methylisoeugenol. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/methylisoeugenol (retrieved
2024-11-08) (BioDeep RN: BioDeep_00000008111). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C/C=C/C1=CC=C(OC)C(OC)=C1
InChI: InChI=1S/C11H14O2/c1-4-5-9-6-7-10(12-2)11(8-9)13-3/h4-8H,1-3H3/b5-4+
描述信息
Cis-isomethyleugenol is an isomethyleugenol.
Isoeugenyl methyl ether is a natural product found in Platostoma africanum, Asarum rigescens, and other organisms with data available.
Constituent of essential oils. Flavouring ingredient. Methylisoeugenol is found in many foods, some of which are star anise, sweet basil, wild carrot, and tarragon.
Methylisoeugenol is found in carrot. Methylisoeugenol is a constituent of essential oils. Methylisoeugenol is a flavouring ingredient.
Methyl isoeugenol (MIE) is a natural food flavour that can be isolated from Pimenta pseudocaryophyllus leaf. Methyl isoeugenol shows anxiolytic and antidepressant like effects. Methyl isoeugenol is orally active[1].
Methyl isoeugenol (MIE) is a natural food flavour that can be isolated from Pimenta pseudocaryophyllus leaf. Methyl isoeugenol shows anxiolytic and antidepressant like effects. Methyl isoeugenol is orally active[1].
同义名列表
67 个代谢物同义名
BENZENE, 1,2-DIMETHOXY-4-(1Z)-1-PROPEN-1-YL-; Benzene, 1,2-dimethoxy-4-(1-propenyl)-, (Z)-; 2-06-00-00918 (Beilstein Handbook Reference); 3-06-00-04995 (Beilstein Handbook Reference); 1,2-dimethoxy-4-[(1Z)-prop-1-en-1-yl]benzene; Benzene, 1,2-dimethoxy-4-(1-propen-1-yl)-; Benzene, 1,2-dimethoxy-4-propenyl-, (Z)-; 1,2-Dimethoxy-4-(1-propenyl)benzene, 9CI; 1,2-dimethoxy-4-[(Z)-prop-1-enyl]benzene; 1,2-DIMETHOXY-4-(1-CIS-PROPENYL)BENZENE; 1,2-Dimethoxy-4-(1-propen-1-yl)benzene; (Z)-3,4-DIMETHOXY-.BETA.-METHYLSTYRENE; 1,2-Dimethoxy-4-(1-Z-propenyl)benzene; 1,2-Dimethoxy-4-(1-e-propenyl)benzene; 1,2-dimethoxy-4-cis-propenyl-benzene; 1,2-Dimethoxy-4-propenyl-(E)-Benzene; 1,2-DIMETHOXY-4-(1-PROPENYL)BENZENE; 1-Propene, 1-(3,4-dimethoxyphenyl)-; 3,4-Dimethoxypropenylbenzene (VAN); 1-(3,4-Dimethoxyphenyl)-1-propene; 1,2-Dimethoxy-4-propenyl-Benzene; 4-Propenyl-1,2-dimethoxybenzene; 1,2-Dimethoxy-4-propenylbenzene; 1,3,4-Isoeugenol methyl ether; ISOEUGENYL METHYL ETHER, CIS-; isomethyleugenol, (E)-isomer; 3,4-Dimethoxypropenylbenzene; VERATROLE, 4-PROPENYL-, CIS-; isomethyleugenol, (Z)-isomer; cis-isoeugenol methyl ether; NNWHUJCUHAELCL-PLNGDYQASA-N; trans-4-Propenylveratrole; cis-isoeugenolmethylether; 4-trans-Propenylveratrole; ghl.PD_Mitscher_leg0.375; cis-4-Propenyl veratrole; trans-Methyl isoeugenol; 4-CIS-PROPENYLVERATROLE; 4-(1-Propenyl)veratrole; Isoeugenol methyl ether; Isoeugenyl methyl ether; trans-Methylisoeugenol; 4-Prop-1-enylveratrole; Methylisoeugenol, (Z)-; trans-isomethyleugenol; (Z)-O-METHYLISOEUGENOL; (E)-Methyl isoeugenol; (Z)-methyl isoeugenol; cis-Methyl isoeugenol; cis-isomethyleugenol; 4-Propenyl veratrole; cis-Methylisoeugenol; 1-Veratryl-1-propene; (Z)-Methylisoeugenol; 4-Propenylveratrole; (e)-methyl eugenol; O-Methylisoeugenol; methyl isoeugenol; Methylisoeugenol; isomethyleugenol; UNII-46RN7Q97DE; UNII-64DPK8DS6F; Isohomogenol; 46RN7Q97DE; 64DPK8DS6F; FEMA 2476; AI3-20967
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:50550
- ChEBI: CHEBI:6877
- KEGG: C10478
- PubChem: 1549045
- PubChem: 7128
- HMDB: HMDB0041553
- Metlin: METLIN68351
- ChEMBL: CHEMBL1164609
- Wikipedia: Methyl isoeugenol
- MeSH: isomethyleugenol
- ChemIDplus: 0000093163
- MetaCyc: ISOMETHYLEUGENOL
- KNApSAcK: C00035131
- KNApSAcK: C00002760
- KNApSAcK: C00050779
- foodb: FDB021536
- chemspider: 21242881
- CAS: 6379-72-2
- CAS: 6380-24-1
- CAS: 93-16-3
- medchemexpress: HY-N2439
- PMhub: MS000021666
- 3DMET: B03883
- NIKKAJI: J15.690F
- LOTUS: LTS0036071
- wikidata: Q27122111
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
代谢反应
17 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(17)
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + isoeugenol ⟶ H+ + SAH + isomethyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + eugenol ⟶ H+ + SAH + methyleugenol
- volatile cinnamoic ester biosynthesis:
SAM + isoeugenol ⟶ H+ + SAH + isomethyleugenol
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
15 个相关的物种来源信息
- 4465 - Acorus calamus: 10.1055/S-0028-1097281
- 55184 - Acorus gramineus:
- 7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 259893 - Artemisia argyi Lévl.et Vant.: -
- 49456 - Asarum europaeum: 10.1055/S-0028-1099525
- 2605041 - Asarum rigescens: 10.1515/ZNC-1984-7-803
- 84873 - Chelonanthus albus: 10.1007/S10600-010-9708-0
- 2815075 - Croton grewioides: 10.1021/JF60217A066
- 9606 - Homo sapiens: -
- 4087 - Nicotiana alata: 10.1016/J.PHYTOCHEM.2006.05.038
- 118694 - Nicotiana bonariensis: 10.1016/J.PHYTOCHEM.2006.05.038
- 33090 - Plants: -
- 204156 - Platostoma africanum: 10.1055/S-2006-962093
- 1223618 - Solidago odora: 10.1016/S0031-9422(00)83939-4
- 399409 - Tagetes filifolia: 10.1080/10412905.1994.9699353
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
- Nina-Katharina Krahe, Ralf G Berger, Franziska Ersoy. A DyP-Type Peroxidase of Pleurotus sapidus with Alkene Cleaving Activity.
Molecules (Basel, Switzerland).
2020 Mar; 25(7):. doi:
10.3390/molecules25071536
. [PMID: 32230972] - Mosaab Yahyaa, Anna Berim, Bhagwat Nawade, Muhammad Ibdah, Natalia Dudareva, Mwafaq Ibdah. Biosynthesis of methyleugenol and methylisoeugenol in Daucus carota leaves: Characterization of eugenol/isoeugenol synthase and O-Methyltransferase.
Phytochemistry.
2019 Mar; 159(?):179-189. doi:
10.1016/j.phytochem.2018.12.020
. [PMID: 30634080] - Xiao-lu Chen, De-jun Yuan, Xue-ru Wu, Qi-duan Wu. [Comparative Study on Quality of Volatile Oil of Acori Tatarinowii Rhizoma from Two Habitats].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2015 Apr; 38(4):770-3. doi:
. [PMID: 26672346]
- Zhibin Wang, Qiuhong Wang, Bingyou Yang, Jing Li, Chunjuan Yang, Yonghai Meng, Haixue Kuang. GC-MS method for determination and pharmacokinetic study of four phenylpropanoids in rat plasma after oral administration of the essential oil of Acorus tatarinowii Schott rhizomes.
Journal of ethnopharmacology.
2014 Sep; 155(2):1134-40. doi:
10.1016/j.jep.2014.06.035
. [PMID: 25046827] - James Oluwagbamigbe Fajemiroye, Pablinny Moreira Galdino, Joelma Abadia Marciano De Paula, Fagundes Fabio Rocha, Moses A Akanmu, Frederico Argollo Vanderlinde, Jordan K Zjawiony, Elson Alves Costa. Anxiolytic and antidepressant like effects of natural food flavour (E)-methyl isoeugenol.
Food & function.
2014 Aug; 5(8):1819-28. doi:
10.1039/c4fo00109e
. [PMID: 24920211] - James Oluwagbamigbe Fajemiroye, Pablinny Moreira Galdino, Suzana Fereirra Alves, Joelma Abadia Marciano de Paula, José Realino de Paula, Paulo Cesár Ghedini, Elson Alves Costa. Involvement of 5-HT1A in the anxiolytic-like effect of dichloromethane fraction of Pimenta pseudocaryophyllus.
Journal of ethnopharmacology.
2012 Jun; 141(3):872-7. doi:
10.1016/j.jep.2012.03.043
. [PMID: 22472106] - Nae Hyung Ryu, Kyung-Ran Park, Sung-Moo Kim, Hyung-Mun Yun, Dongwoo Nam, Seok-Geun Lee, Hyeung-Jin Jang, Kyoo Seok Ahn, Sung-Hoon Kim, Bum Sang Shim, Seung-Hoon Choi, Ashik Mosaddik, Somi K Cho, Kwang Seok Ahn. A hexane fraction of guava Leaves (Psidium guajava L.) induces anticancer activity by suppressing AKT/mammalian target of rapamycin/ribosomal p70 S6 kinase in human prostate cancer cells.
Journal of medicinal food.
2012 Mar; 15(3):231-41. doi:
10.1089/jmf.2011.1701
. [PMID: 22280146] - Deepa Bisht, Anirban Pal, C S Chanotiya, Dhirendra Mishra, K N Pandey. Terpenoid composition and antifungal activity of three commercially important essential oils against Aspergillus flavus and Aspergillus niger.
Natural product research.
2011 Dec; 25(20):1993-8. doi:
10.1080/14786419.2010.521926
. [PMID: 21707253] - Xiao-Gang Tong, Gui-Sheng Wu, Cheng-Gang Huang, Qing Lu, Yue-Hu Wang, Chun-Lin Long, Huai-Rong Luo, Hua-Jie Zhu, Yong-Xian Cheng. Compounds from Acorus tatarinowii: determination of absolute configuration by quantum computations and cAMP regulation activity.
Journal of natural products.
2010 Jun; 73(6):1160-3. doi:
10.1021/np900793e
. [PMID: 20476749] - Jeong-Yeh Yang, Mary Anne Della-Fera, Srujana Rayalam, Hea Jin Park, Suresh Ambati, Dorothy B Hausman, Diane L Hartzell, Clifton A Baile. Regulation of adipogenesis by medium-chain fatty acids in the absence of hormonal cocktail.
The Journal of nutritional biochemistry.
2009 Jul; 20(7):537-43. doi:
10.1016/j.jnutbio.2008.05.013
. [PMID: 18789670] - Zi-min Yuan, Jing Wang, Jial Lv, Tian-zhu Jia. [Comparing analysis of components in volatile oils of nutmeg and prepared nutmeg by GC-MS].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2006 May; 31(9):737-9. doi:
"
. [PMID: 17048680] - N M Cuong, W C Taylor, V T Sung. A new cyclobutane lignan from Cinnamomum balansae.
Natural product letters.
2001; 15(5):331-8. doi:
10.1080/10575630108041300
. [PMID: 11841117] - T Jia, M Sha, A Cao, Z Wamg, F Xia. [Determination of eugenol, methyleugenol and methylisoeugenol in volatile oil of differently processed nutmeg].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
1997 Aug; 22(8):474-5, 511. doi:
. [PMID: 11038913]
- R Purchase, G P Ford, D M Creasy, P G Brantom, S D Gangolli. A 28-day feeding study with methyl isoeugenol in rats.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
1992 Jun; 30(6):475-81. doi:
10.1016/0278-6915(92)90098-6
. [PMID: 1386830] - . .
.
. doi:
. [PMID: 9159948]
- . .
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. doi:
. [PMID: 18987218]