TMPEA (BioDeep_00000861395)

Main id: BioDeep_00000001490

 


代谢物信息卡片


4-13-00-02919 (Beilstein Handbook Reference)

化学式: C11H17NO3 (211.1208)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC(=CC(=C1OC)OC)CCN
InChI: InChI=1S/C11H17NO3/c1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3/h6-7H,4-5,12H2,1-3H3

描述信息

D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists
D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens

同义名列表

35 个代谢物同义名

4-13-00-02919 (Beilstein Handbook Reference); Ethane, 1-amino-2-(3,4,5-trimethoxyphenyl)-; Benzeneethanamine, 3,4,5-trimethoxy- (9CI); Phenethylamine, 3,4,5-trimethoxy- (8CI); 2-(3,4,5-trimethoxyphenyl)ethanamine; Benzeneethanamine, 3,4,5-trimethoxy-; 2-(3,4,5-Trimethoxyphenyl)ethylamine; 3,4,5-Trimethoxy-b-phenethylamine; 3,4,5-Trimethoxybenzeneethanamine; Phenethylamine, 3,4,5-trimethoxy-; 3,4,5-Trimethoxyphenylethylamine; Constituent of \"Peyote\" cacti; 3,4,5-Trimethoxyphenethylamine; WLN: Z2R CO1 DO1 EO1; Mescalin [German]; EINECS 200-190-7; DivK1c_000984; Oprea1_166025; DEA No. 7381; KBio1_000984; NINDS_000984; BRN 1374088; IDI1_000984; mescaline; Mezcaline; NSC 30419; Mescalin; NSC30419; Mezcalin; Mescline; Mezcline; 54-04-6; C06546; TMPEA; Mescaline



数据库引用编号

11 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)

41 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。

亚细胞结构定位 关联基因列表
Cytoplasm 7 AOC3, CYP2D6, DDC, MAP2, MAP4K4, PHB1, POU5F1
Peripheral membrane protein 1 CYP1B1
Endoplasmic reticulum membrane 3 CYP1B1, CYP2D6, TAAR1
Nucleus 6 CDX2, LHX6, NANOG, NKX2-1, PHB1, POU5F1
cytosol 3 DDC, MAP2, POU5F1
dendrite 5 GRM2, HTR1A, HTR2A, HTR2C, MAP2
nucleoplasm 5 CDX2, NANOG, NKX2-1, PHB1, POU5F1
Cell membrane 8 AOC3, GRM2, GRM3, HTR1A, HTR2A, HTR2C, PHB1, TAAR1
Cell projection, axon 1 HTR2A
Multi-pass membrane protein 6 GRM2, GRM3, HTR1A, HTR2A, HTR2C, TAAR1
Synapse 3 GRM2, HTR1A, HTR2C
cell surface 2 AOC3, PHB1
dendritic shaft 2 HTR2A, MAP2
glutamatergic synapse 3 GRM2, GRM3, HTR2A
Golgi apparatus 1 AOC3
mitochondrial inner membrane 1 PHB1
neuronal cell body 2 HTR2A, MAP2
presynaptic membrane 3 GRM2, GRM3, HTR2A
Presynapse 1 HTR2A
plasma membrane 9 AOC3, BCHE, GRM2, GRM3, HTR1A, HTR2A, HTR2C, PHB1, TAAR1
Membrane 6 AOC3, CYP1B1, CYP2D6, GRM2, GRM3, PHB1
axon 3 GRM2, GRM3, HTR2A
caveola 1 HTR2A
extracellular exosome 2 DDC, PHB1
endoplasmic reticulum 2 AOC3, CYP2D6
extracellular space 2 BCHE, CPZ
mitochondrion 4 CYP1B1, CYP2D6, PHB1, POU5F1
intracellular membrane-bounded organelle 3 CYP1B1, CYP2D6, NANOG
Microsome membrane 2 CYP1B1, CYP2D6
postsynaptic density 1 GRM3
Secreted 1 BCHE
extracellular region 1 BCHE
Single-pass membrane protein 1 CYP2D6
transcription regulator complex 2 NKX2-1, POU5F1
Secreted, extracellular space, extracellular matrix 1 CPZ
dendritic spine 1 GRM3
cytoplasmic vesicle 1 HTR2A
nucleolus 1 NANOG
Early endosome 2 AOC3, PHB1
Single-pass type II membrane protein 1 AOC3
postsynaptic membrane 3 GRM2, GRM3, HTR2A
Mitochondrion inner membrane 1 PHB1
Cytoplasm, cytoskeleton 1 MAP2
focal adhesion 1 MAP4K4
microtubule 1 MAP2
dendrite cytoplasm 1 MAP2
neuron projection 1 MAP2
chromatin 5 CDX2, LHX6, NANOG, NKX2-1, POU5F1
microtubule associated complex 1 MAP2
blood microparticle 1 BCHE
Endomembrane system 1 TAAR1
microvillus 1 AOC3
Membrane, caveola 1 HTR2A
cell body fiber 1 HTR2A
axon initial segment 1 MAP2
Cell projection, dendrite 4 GRM2, HTR1A, HTR2A, MAP2
dendritic growth cone 1 MAP2
endoplasmic reticulum lumen 1 BCHE
transcription repressor complex 1 CDX2
proximal neuron projection 1 MAP2
nuclear envelope lumen 1 BCHE
condensed nuclear chromosome 1 CDX2
neurofilament 1 HTR2A
axon hillock 1 MAP2
basal dendrite 1 MAP2
astrocyte projection 2 GRM2, GRM3
apical distal dendrite 1 MAP2
dendritic branch 1 MAP2
dendritic filopodium 1 MAP2
distal dendrite 1 MAP2
primary dendrite 1 MAP2
proximal dendrite 1 MAP2
G protein-coupled serotonin receptor complex 2 HTR2A, HTR2C
mitochondrial prohibitin complex 1 PHB1


文献列表

  • Lucas Apolinário Chibli, Bruna Ribeiro de Lima, Ariadne Magalhães Carneiro, Harley Cardoso Figueiró, Serhat Sezai Cicek, Verena Spiegler, Cristiano Soleo Funari. Toward a More Sustainable Sample Preparation in Phytochemistry: Case Studies in Four Subclasses of Alkaloids. Journal of natural products. 2024 Mar; 87(3):470-479. doi: 10.1021/acs.jnatprod.3c01048. [PMID: 38381880]
  • Gwendolyn K Kirschner. Breaking bad buttons: mescaline biosynthesis in peyote. The Plant journal : for cell and molecular biology. 2023 11; 116(3):633-634. doi: 10.1111/tpj.16503. [PMID: 37861456]
  • Jacinta L Watkins, Qiushi Li, Sam Yeaman, Peter J Facchini. Elucidation of the mescaline biosynthetic pathway in peyote (Lophophora williamsii). The Plant journal : for cell and molecular biology. 2023 Sep; ?(?):. doi: 10.1111/tpj.16447. [PMID: 37675639]
  • Minji Lee, Ju Yeon Jung, Sungsoo Choi, Ilung Seol, Seohyun Moon, In Kwan Hwang. Single Nucleotide Polymorphism Assay for Genetic Identification of Lophophora williamsii. Journal of forensic sciences. 2020 Nov; 65(6):2117-2120. doi: 10.1111/1556-4029.14515. [PMID: 32725909]
  • Cameron M Longo, Rabi A Musah. An Efficient Ambient Ionization Mass Spectrometric Approach to Detection and Quantification of the Mescaline Content of Commonly Abused Cacti from the Echinopsis Genus. Journal of forensic sciences. 2020 Jan; 65(1):61-66. doi: 10.1111/1556-4029.14134. [PMID: 31310334]
  • William E Rosa, Stephanie Hope, Marianne Matzo. Palliative Nursing and Sacred Medicine: A Holistic Stance on Entheogens, Healing, and Spiritual Care. Journal of holistic nursing : official journal of the American Holistic Nurses' Association. 2019 Mar; 37(1):100-106. doi: 10.1177/0898010118770302. [PMID: 29669454]
  • Abigail Moreno-Pedraza, Ignacio Rosas-Román, Nancy Shyrley Garcia-Rojas, Héctor Guillén-Alonso, Cesaré Ovando-Vázquez, David Díaz-Ramírez, Jessica Cuevas-Contreras, Fredd Vergara, Nayelli Marsch-Martínez, Jorge Molina-Torres, Robert Winkler. Elucidating the Distribution of Plant Metabolites from Native Tissues with Laser Desorption Low-Temperature Plasma Mass Spectrometry Imaging. Analytical chemistry. 2019 02; 91(4):2734-2743. doi: 10.1021/acs.analchem.8b04406. [PMID: 30636413]
  • Bruce K Cassels, Patricio Sáez-Briones. Dark Classics in Chemical Neuroscience: Mescaline. ACS chemical neuroscience. 2018 10; 9(10):2448-2458. doi: 10.1021/acschemneuro.8b00215. [PMID: 29847089]
  • Adrienne E Ng, Ernesto Sandoval, Terence M Murphy. Identification and Individualization of Lophophora using DNA Analysis of the trnL/trnF Region and rbcL Gene. Journal of forensic sciences. 2016 Jan; 61 Suppl 1(?):S226-9. doi: 10.1111/1556-4029.12936. [PMID: 27405021]
  • Dilek Battal, Allan J Barnes, Marisol S Castaneto, Thomas M Martin, Kevin L Klette, Marilyn A Huestis. Urine Mescaline Screening With a Biochip Array Immunoassay and Quantification by Gas Chromatography-Mass Spectrometry. Therapeutic drug monitoring. 2015 Dec; 37(6):805-11. doi: 10.1097/ftd.0000000000000220. [PMID: 25992796]
  • Enrique Ibarra-Laclette, Flor Zamudio-Hernández, Claudia Anahí Pérez-Torres, Victor A Albert, Enrique Ramírez-Chávez, Jorge Molina-Torres, Araceli Fernández-Cortes, Carlos Calderón-Vázquez, José Luis Olivares-Romero, Alfredo Herrera-Estrella, Luis Herrera-Estrella. De novo sequencing and analysis of Lophophora williamsii transcriptome, and searching for putative genes involved in mescaline biosynthesis. BMC genomics. 2015 Sep; 16(?):657. doi: 10.1186/s12864-015-1821-9. [PMID: 26330142]
  • Cristiana Gambelunghe, Remo Marsili, Kyriaki Aroni, Mauro Bacci, Riccardo Rossi. GC-MS and GC-MS/MS in PCI mode determination of mescaline in peyote tea and in biological matrices. Journal of forensic sciences. 2013 Jan; 58(1):270-8. doi: 10.1111/j.1556-4029.2012.02249.x. [PMID: 22900815]
  • S Lerch, K J Shingfield, A Ferlay, A Vanhatalo, Y Chilliard. Rapeseed or linseed in grass-based diets: effects on conjugated linoleic and conjugated linolenic acid isomers in milk fat from Holstein cows over 2 consecutive lactations. Journal of dairy science. 2012 Dec; 95(12):7269-87. doi: 10.3168/jds.2012-5654. [PMID: 22999291]
  • Christine A Strick, Cheryl Li, Liam Scott, Brian Harvey, Mihály Hajós, Stefanus J Steyn, Mary A Piotrowski, Larry C James, James T Downs, Brian Rago, Stacey L Becker, Ayman El-Kattan, Youfen Xu, Alan H Ganong, F David Tingley, Andres D Ramirez, Patricia A Seymour, Victor Guanowsky, Mark J Majchrzak, Carol B Fox, Christopher J Schmidt, Allen J Duplantier. Modulation of NMDA receptor function by inhibition of D-amino acid oxidase in rodent brain. Neuropharmacology. 2011 Oct; 61(5-6):1001-15. doi: 10.1016/j.neuropharm.2011.06.029. [PMID: 21763704]
  • Masako Aragane, Yohei Sasaki, Jun'ichi Nakajima, Nobutaka Fukumori, Masao Yoshizawa, Yukiko Suzuki, Shigemi Kitagawa, Ken'ichiro Mori, Shuzo Ogino, Ichiro Yasuda, Seiji Nagumo. Peyote identification on the basis of differences in morphology, mescaline content, and trnL/trnF sequence between Lophophora williamsii and L. diffusa. Journal of natural medicines. 2011 Jan; 65(1):103-10. doi: 10.1007/s11418-010-0469-7. [PMID: 20890669]
  • Olabode Ogunbodede, Douglas McCombs, Keeper Trout, Paul Daley, Martin Terry. New mescaline concentrations from 14 taxa/cultivars of Echinopsis spp. (Cactaceae) ('San Pedro') and their relevance to shamanic practice. Journal of ethnopharmacology. 2010 Sep; 131(2):356-62. doi: 10.1016/j.jep.2010.07.021. [PMID: 20637277]
  • Kristian Björnstad, Anders Helander, Olof Beck. Development and clinical application of an LC-MS-MS method for mescaline in urine. Journal of analytical toxicology. 2008 Apr; 32(3):227-31. doi: 10.1093/jat/32.3.227. [PMID: 18397574]
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  • L Demisch, P Kaczmarczyk, N Seiler. 3,4,5-Trimethoxybenzoic acid, a new mescaline metabolite in humans. Drug metabolism and disposition: the biological fate of chemicals. 1978 Sep; 6(5):507-9. doi: NULL. [PMID: 30599]
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  • R A Roth, J A Roth, C N Gillis. Disposition of 14C-mescaline by rabbit lung. The Journal of pharmacology and experimental therapeutics. 1977 Feb; 200(2):394-401. doi: NULL. [PMID: 839444]
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  • L J Riceberg, M Simon, H Van Vunakis, R H Abeles. Effects of aminoacetonitrile, an amine oxidase inhibitor, on mescaline metabolism in the rabbit. Biochemical pharmacology. 1975 Jan; 24(1):119-25. doi: 10.1016/0006-2952(75)90323-8. [PMID: 1168468]
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