Myristicin (BioDeep_00000000888)

 

Secondary id: BioDeep_00000859510

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


1-Methoxy-2,3-methylenedioxy-5-(2-propenyl)benzene

化学式: C11H12O3 (192.0786402)
中文名称: 肉豆蔻醚, 肉豆蔻碱, 肉豆蔻
谱图信息: 最多检出来源 unclassified Codonopsis(otcml) 9.73%

分子结构信息

SMILES: C=CCC1=CC(OC)=C2OCOC2=C1
InChI: InChI=1S/C11H12O3/c1-3-4-8-5-9(12-2)11-10(6-8)13-7-14-11/h3,5-6H,1,4,7H2,2H3

描述信息

Myristicin is an organic molecular entity. It has a role as a metabolite.
Myristicin is a natural product found in Chaerophyllum azoricum, Peperomia bracteata, and other organisms with data available.
Myristicin is found in anise. Myristicin is a constituent of dill, nutmeg, parsley and many other essential oils. May be responsible for psychotic effects of nutmeg at large doses Myristicin, 3-methoxy,4,5-methylendioxy-allylbenzene, is a natural organic compound present in the essential oil of nutmeg and to a lesser extent in other spices such as parsley and dill. Myristicin is a naturally occurring insecticide and acaricide with possible neurotoxic effects on dopaminergic neurons[citation needed]. It has hallucinogenic properties at doses much higher than used in cooking. Myristicin is a weak inhibitor of monoamine oxidase.Myristicin has been shown to exhibit apoptotic and hepatoprotective functions (A7836, A7837).Myristicin belongs to the family of Benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole.
Myristicin is found in anise. Myristicin is a constituent of dill, nutmeg, parsley and many other essential oils. May be responsible for psychotic effects of nutmeg at large doses Myristicin, 3-methoxy,4,5-methylendioxy-allylbenzene, is a natural organic compound present in the essential oil of nutmeg and to a lesser extent in other spices such as parsley and dill. Myristicin is a naturally occurring insecticide and acaricide with possible neurotoxic effects on dopaminergic neurons[citation needed]. It has hallucinogenic properties at doses much higher than used in cooking. Myristicin is a weak inhibitor of monoamine oxidase
Constituent of dill, nutmeg, parsley and many other essential oils. May be responsible for psychotic effects of nutmeg at large doses
Myristicine ?act as a serotonin receptor antagonist, a weak monamine oxidase (MAO) inhibitor. Myristicine is the main component of nutmeg essential oil from Myristica fragrans?Houtt. Myristicine abuse produce hallucinogenic effects, organ damage, deliriumand others[1].
Myristicine is an orally bioavailable serotonin receptor antagonist and weak monoamine oxidase (MAO) inhibitor. Myristicine also exerts anti-cancer effects on gastric cancer cells by inhibiting the EGFR/ERK signaling pathway. Myristicine is the main component of nutmeg essential oil and has anti-cancer, anti-proliferative, antibacterial, anti-inflammatory and apoptosis-inducing effects. Myristicine abuse can produce hallucinogenic effects, organ damage, etc[1][2][3][4].
Myristicine is an orally bioavailable serotonin receptor antagonist and weak monoamine oxidase (MAO) inhibitor. Myristicine also exerts anti-cancer effects on gastric cancer cells by inhibiting the EGFR/ERK signaling pathway. Myristicine is the main component of nutmeg essential oil and has anti-cancer, anti-proliferative, antibacterial, anti-inflammatory and apoptosis-inducing effects. Myristicine abuse can produce hallucinogenic effects, organ damage, etc[1][2][3][4].
Myristicine ?act as a serotonin receptor antagonist, a weak monamine oxidase (MAO) inhibitor. Myristicine is the main component of nutmeg essential oil from Myristica fragrans?Houtt. Myristicine abuse produce hallucinogenic effects, organ damage, deliriumand others[1].

同义名列表

33 个代谢物同义名

1-Methoxy-2,3-methylenedioxy-5-(2-propenyl)benzene; 1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)- (9CI); Benzene, 5-allyl-1-methoxy-2,3-(methylenedioxy)-; 4-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole; 4-Methoxy-6-(2-propenyl)-1,3-benzodioxole, 9CI; 5-Allyl-1-methoxy-2,3-(methylenedioxy)-Benzene; 5-allyl-1-methoxy-2,3-(methylenedioxy)benzene; 5-19-02-00631 (Beilstein Handbook Reference); 5-ALLYL-1-METHOXY-2,3-METHYLENEDIOXYBENZENE; 1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)-; 1-Allyl-3-methoxy-4,5-methylenedioxybenzene; 4-Methoxy-6-(2-propenyl)-1,3-benzodioxole; 6-ALLYL-1,3-BENZODIOXOL-4-YL METHYL ETHER; 4-Methoxy-6-[2-propenyl]-1,3-benzodioxole; 4-methoxy-6-prop-2-enyl-1,3-benzodioxole; 6-allyl-4-methoxybenzo[d][1,3]dioxole; 6-allyl-4-methoxy-benzo-1,3-dioxole; 6-Allyl-4-methoxy-1,3-benzodioxole; 5-Allyl-2,3-(methylendioxy)anisole; Myristicin from parsley leaf oil; Myristicin, analytical standard; MYRISTICIN [HSDB]; Myristicin (6CI); Myristicin_major; MYRISTICIN [MI]; UNII-04PD6CT78W; Tox21_200172; Myristicine; Myristicin; 04PD6CT78W; asaricin; Myristicin; Myristicin



数据库引用编号

22 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)

270 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

  • Mostafa H Baky, Eman M El-Taher, Dina M Y El Naggar, Mostafa B Abouelela. Phytochemical investigation of the n-hexane-extracted oil from four umbelliferous vegetables using GC/MS analysis in the context of antibacterial activity. Scientific reports. 2024 05; 14(1):10592. doi: 10.1038/s41598-024-60631-4. [PMID: 38719900]
  • Ly Thi Huong Nguyen, Nhi Phuc Khanh Nguyen, Khoa Nguyen Tran, Heung-Mook Shin, In-Jun Yang. Intranasal administration of the essential oil from Perillae Folium ameliorates social defeat stress-induced behavioral impairments in mice. Journal of ethnopharmacology. 2024 Jan; 324(?):117775. doi: 10.1016/j.jep.2024.117775. [PMID: 38224793]
  • Jin Song, Xiaolong Xu, Shasha He, Ning Wang, Yunjing Bai, Zhaoxia Chen, Bo Li, Shengsheng Zhang. Myristicin Suppresses Gastric Cancer Growth via Targeting the EGFR/ERK Signaling Pathway. Current molecular pharmacology. 2023 Jan; ?(?):. doi: 10.2174/1874467216666230103104600. [PMID: 36597605]
  • Huda M Ismail Abo El-Fadl, Mamdouh F A Mohamed. Targeting endoplasmic reticulum stress, Nrf-2/HO-1, and NF-κB by myristicin and its role in attenuation of ulcerative colitis in rats. Life sciences. 2022 Dec; 311(Pt B):121187. doi: 10.1016/j.lfs.2022.121187. [PMID: 36403646]
  • Fawang Liu, Tahir Ali, Zhong Liu. Physiological, Biochemical and Transcriptomic Analysis of the Aerial Parts (Leaf-Blade and Petiole) of Asarum sieboldii Responding to Drought Stress. International journal of molecular sciences. 2021 Dec; 22(24):. doi: 10.3390/ijms222413402. [PMID: 34948197]
  • Xin-Xin Lu, Na-Na Hu, Yue-Shen Du, Borjigidai Almaz, Xu Zhang, Shu-Shan Du. Chemical compositions and repellent activity of Clerodendrum bungei Steud. essential oil against three stored product insects. Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences. 2021 Dec; 29(2):469-475. doi: 10.1007/s40199-021-00398-5. [PMID: 34142352]
  • Thidar Oo, Bhanubong Saiboonjan, Sukanya Srijampa, Arpasiri Srisrattakarn, Khaetthareeya Sutthanut, Ratree Tavichakorntrakool, Aroonwadee Chanawong, Aroonlug Lulitanond, Patcharaporn Tippayawat. Inhibition of Bacterial Efflux Pumps by Crude Extracts and Essential Oil from Myristica fragrans Houtt. (Nutmeg) Seeds against Methicillin-Resistant Staphylococcus aureus. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154662. [PMID: 34361815]
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  • Paulina Laszuk, Aneta D Petelska. Interactions between Phosphatidylcholine and Kaempferol or Myristicin: Langmuir Monolayers and Microelectrophoretic Studies. International journal of molecular sciences. 2021 Apr; 22(9):. doi: 10.3390/ijms22094729. [PMID: 33946951]
  • Chia-Jung Lee, Chun-Wei Huang, Lih-Geeng Chen, Ching-Chiung Wang. (+)-Erythro-Δ8'-7S,8R-Dihydroxy-3,3',5'-Trimethoxy-8-O-4'-Neolignan, an Anti-Acne Component in Degreasing Myristica fragrans Houtt. Molecules (Basel, Switzerland). 2020 Oct; 25(19):. doi: 10.3390/molecules25194563. [PMID: 33036279]
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  • Ai-Hong Yang, Xin He, Jun-Xiu Chen, Li-Na He, Chun-Huan Jin, Li-Li Wang, Fang-Liang Zhang, Li-Jun An. Identification and characterization of reactive metabolites in myristicin-mediated mechanism-based inhibition of CYP1A2. Chemico-biological interactions. 2015 Jul; 237(?):133-40. doi: 10.1016/j.cbi.2015.06.018. [PMID: 26091900]
  • Víctor López, Javier Gerique, Elisa Langa, César Berzosa, Marta Sofía Valero, Carlota Gómez-Rincón. Antihelmintic effects of nutmeg (Myristica fragans) on Anisakis simplex L3 larvae obtained from Micromesistius potassou. Research in veterinary science. 2015 Jun; 100(?):148-52. doi: 10.1016/j.rvsc.2015.03.033. [PMID: 25890576]
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  • Detlef Ulrich, Thomas Nothnagel, Hartwig Schulz. Influence of cultivar and harvest year on the volatile profiles of leaves and roots of carrots (Daucus carota spp. sativus Hoffm.). Journal of agricultural and food chemistry. 2015 Apr; 63(13):3348-56. doi: 10.1021/acs.jafc.5b00704. [PMID: 25797828]
  • Xin Chao Liu, Zhi Long Liu. Analysis of the essential oil of Illicium henryi Diels root bark and its insecticidal activity against Liposcelis bostrychophila Badonnel. Journal of food protection. 2015 Apr; 78(4):772-7. doi: 10.4315/0362-028x.jfp-14-407. [PMID: 25836404]
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  • Guido Flamini, Tahar Smaili, Amar Zellagui, Noureddine Gherraf, Pier Luigi Cioni. Effect of growth stage on essential-oil yield and composition of Daucus sahariensis. Chemistry & biodiversity. 2013 Nov; 10(11):2014-20. doi: 10.1002/cbdv.201300052. [PMID: 24243610]
  • Phurpa Wangchuk, Paul A Keller, Stephen G Pyne, Malai Taweechotipatr, Sumalee Kamchonwongpaisan. GC/GC-MS analysis, isolation and identification of bioactive essential oil components from the Bhutanese medicinal plant, Pleurospermum amabile. Natural product communications. 2013 Sep; 8(9):1305-8. doi: . [PMID: 24273872]
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