Relevant bibliographies by topics / Ethylamine

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'Ethylamine'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 July 2025

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Journal articles on the topic "Ethylamine"

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Ashihara, Hiroshi. "Occurrence, Biosynthesis and Metabolism of Theanine (γ-Glutamyl-L-ethylamide) in Plants: A Comprehensive Review". Natural Product Communications 10, № 5 (2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000525.

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Theanine (γ-glutamyl-L-ethylamide) is the most abundant non-protein amino acid in tea leaves. In addition to Camellia sinensis, theanine occurs in several plants belonging to the Ericales. Biosynthesis of theanine from glutamic acid and ethylamine by theanine synthetase is present in all organs of tea seedlings, but roots are the major site of theanine biosynthesis in adult tea trees. Theanine is transported from roots to young leaves via the xylem sap. Theanine is hydrolysed to glutamic acid and ethylamine in leaves. Ethylamine produced from theanine is predominantly used for catechin biosynt
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Angelov, Plamen, Paraskeva Terziyska, and Danail Georgiev. "3-(1-Ethylamino-ethylidene)-1-methyl-pyrrolidine-2,4-dione." Molbank 2023, no. 1 (2023): M1556. http://dx.doi.org/10.3390/m1556.

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3-(1-Ethylamino-ethylidene)-1-methyl-pyrrolidine-2,4-dione was obtained as an unexpected product in a three-step synthesis starting with o-nitrobenzoyl sarcosine, acetoacetanilide and ethylamine. The compound showed moderate antibacterial activity against S. aureus and E. coli.
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Deng, Wei-Wei, Shinjiro Ogita, and Hiroshi Ashihara. "Ethylamine Content and Theanine Biosynthesis in Different Organs of Camellia sinensis Seedlings." Zeitschrift für Naturforschung C 64, no. 5-6 (2009): 387–90. http://dx.doi.org/10.1515/znc-2009-5-614.

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We examined the distribution of ethylamine, glutamic acid and alanine, which are utilized in theanine biosynthesis, and other major amino acids in leaves, stems, cotyledons and roots of 6-week-old tea seedlings. Ethylamine and glutamic acid, which are substrates of theanine synthetase, were distributed almost uniformly in all parts of the seedlings; the contents in μmol/g fresh wt varied from 0.44 - 0.88 (ethylamine) and 1.6 - 2.4 (glutamic acid). The content of alanine, a possible precursor of ethylamine synthesis, was significantly higher in roots (3.1 μmol/g fresh wt) than in other parts. I
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Wenceslau, João P. S., Dávila F. de Souza, Maria C. F. de Oliveira, et al. "Novel Lapachol Derivatives and Their Antioxidant Activity." Natural Product Communications 1, no. 8 (2006): 1934578X0600100. http://dx.doi.org/10.1177/1934578x0600100812.

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A convenient synthesis of the new enamine derivatives 2-diethylamino-3-(3-methyl-2-butenyl)-1,4-naphthalenedione (2), 2-ethylamino-3-(3-methyl-2-butenyl)-1,4-naphthalenedione (3), 2-diethanolamino-3-(3-methyl-2-butenyl)-1,4-naphthalenedione (4), and 2-(1-piperazinyl)-3-(3-methyl-2-butenyl)-1,4-naphthalenedione (5) was carried out from natural 2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphtalenedione (lapachol, 1) and diethylamine, ethylamine, diethanolamine and piperazine, respectively. All products were fully characterized by IR, 1H and 13C NMR spectroscopy. Results revealed no antioxidant behavio
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Schur, Michael, Christian Näther, and Wolfgang Bensch. "Synthesis and Crystal Structure of Mn2(C2H5NH2)2Sb2S5 Exhibiting a Reversible Phase Transition." Zeitschrift für Naturforschung B 56, no. 1 (2001): 79–84. http://dx.doi.org/10.1515/znb-2001-0113.

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Abstract Thioantimonates, Solvothermal Synthesis, Chalcogenides The reaction of elemental manganese, antimony and sulfur with ethylamine under mild solvothermal conditions yielded a thioantimonate(III) with composition Mn2(EA)2Sb2S5 (EA = C2H5NH2) that is a new member of a series of polymeric manganese thioantimo-nates(III). The structure of the title compound consists of layers of a neutral mesh-like Mn2Sb2S5 framework. The ethylamino ligands coordinated to the Mn centres separate the sheets and fill the voids within the layers formed by the interconnection of Mn2Sb2S4 hetero-cubane like buil
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Xia, Rong, and Feng Jiao. "Electrosynthesis of Value-Added Chemicals Using Water As a Proton Source." ECS Meeting Abstracts MA2022-02, no. 53 (2022): 2469. http://dx.doi.org/10.1149/ma2022-02532469mtgabs.

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Electrifying chemical productions is a potential approach to decarbonizing the chemical industry. The electrochemical processes, when powered by renewable electricity, have lower carbon footprints than conventional thermochemical routes. Using water as the proton source avoids the energy-intensive dry-reforming process to produce H2 from fossil fuels, and electrochemical reaction using voltage as driving force instead of elevated pressure enables the reaction to happen at ambient temperature and pressure. Electrosynthesis of value-added ethylamine and ethylene glycol are used as two examples i
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Peng, Zhenmeng, Yanlin Zhu, Jinyao Tang, Jialu Li, and Dezhen Wu. "Enabling Ethylamine as an Electrochemical Liquid Organic Hydrogen Carrier." ECS Meeting Abstracts MA2025-01, no. 29 (2025): 1568. https://doi.org/10.1149/ma2025-01291568mtgabs.

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Efficient and safe hydrogen storage remains a critical challenge for the advancement of a clean and sustainable hydrogen economy. Traditional storage methods, such as compressed gas and cryogenic liquids, face limitations in energy efficiency, safety, and storage capacity, falling short of the U.S. Department of Energy's 2025 onboard hydrogen storage target of 5.5 wt.% under moderate conditions. Liquid organic hydrogen carriers (LOHCs) offer a promising alternative by enabling hydrogen storage through reversible hydrogenation and dehydrogenation reactions. While thermochemical LOHC systems are
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Zhang, Zheng Zhu, Shou He Yan, Da Xiang Li, Tie Jun Ling, Marc Meurens, and Yvan Larondelle. "Chemical Synthesis and the Stability of Theanine." Advanced Materials Research 396-398 (November 2011): 1273–77. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.1273.

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A chemical synthesis procedure for theanine from L-pyrrolidonecarboxylic acid (L-PCA) and ethylamine was modified. L-PCA was allowed to react with excess anhydrous ethylamine (>99%) to produce theanine at 35°C for 10 days. The theanine crystallized from 84% ethanol (V/V) at 4°C with yield of 17-30%. Results shown that L-PCA was conversed into theanine and a 98.2% yield of theanine was obtained by freeze-drying of the reacted mixture directly after reaction in the same manner. The synthesized products were identified by 1H-NMR and MS analysis. Both the isomers existed in products while the L
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Mitchell, S. C., A. Q. Zhang, and R. L. Smith. "Ethylamine in human urine." Clinica Chimica Acta 302, no. 1-2 (2000): 69–78. http://dx.doi.org/10.1016/s0009-8981(00)00355-7.

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Collin, Jacques. "Dissociation and Rearrangement Processes in Ethylamine and Ethylamine-2d2 by Electron Impact." Bulletin des Sociétés Chimiques Belges 67, no. 9-10 (2010): 549–59. http://dx.doi.org/10.1002/bscb.19580670902.

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Dissertations / Theses on the topic "Ethylamine"

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Yousfi, Abdellah. "Hydrogénation catalytique en phase homogène : synthèse de la 2-thienyl-2-ethylamine à partir du 2-nitrovinyl-2-thiophène." Toulouse 3, 1992. http://www.theses.fr/1992TOU30001.

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L'objectif du travail presente etait la recherche de catalyseurs de reduction catalytique en phase homogene du 2-nitrovinyl-2-thiophene (nvt) en 2-thienylethylamine (tea). Deux systemes reducteurs ont ete etudies: 1) le melange co+h#2o avec comme catalyseur ru#3(co)#1#2 en milieu basique. La reduction s'arrete au stade du thienylacetaldehyde oxime avec une selectivite maximale de 40% pour 100% de conversion du nvt. 2) la reduction sous pression d'hydrogene avec comme catalyseur ru#3(co)#1#2, h#4ru#4(co)#1#2 substitues ou non par des phosphines et des complexes mononucleaires ruh#xx#2##x(co)#y(
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Niemetz, Markus. "Chelatliganden mit 1-(Pyridin-2-yl)ethylamin als chiralem Baustein." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=962784028.

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DU, MOULIN DE LA BRETECHE MARIE-LAURE. "Modification de composes aromatiques en conditions douces : bioconversion de la 2-chloro 4-ethylamino 6-isopropylamino 1,3,5-triazine ou atrazine ; etude de la nitrosation de phenols substitues et des catecholamines." Paris 11, 1994. http://www.theses.fr/1994PA112320.

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La chimie en conditions douces s'avere une alternative de choix, a la fois lors de l'etude de molecules sensibles aux conditions de ph et d'oxydo-reduction, et lors de l'etude des processus physiologiques. L'illustration de ces methodes a ete realisee dans le cas de la biodegradation de l'atrazine, herbicide qui s'accumule dans les sols et dans l'eau et de la reactivite des nitrites sur les phenols. La bioconversion de l'atrazine a ete effectuee par des microorganismes issus du milieu naturel. Les champignons filamenteux rhizopus arrhizus, curvularia lunata et beauveria bassiana transforment l
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Lin, Wang-Jong, and 林王忠. "A study of the electrophysiological effect of N-allyl-N- methyl-2- (3,4-methylenedioxyphenyl)-ethylamine (HF-Ⅴ-15) on cardiac tissues." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/90768512568572360468.

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碩士<br>國立臺灣大學<br>藥理學研究所<br>84<br>HF-Ⅴ-15 是合成小分子生物鹼，在大白鼠心臟組織具有稍微增加收縮力 及減慢心跳頻率的作用。本篇論文主要研究 HF-Ⅴ-15 在大白鼠及天竺鼠 心臟組織的電生理學，並研究其抗心律不整的作用機轉。 1、在大白鼠心 房及心室組織，HF-Ⅴ-15 (3∼30μM) 會使收縮力隨濃度增加而略為增強 ，並使右心房自發性跳動頻率減慢。 2、在離體天竺鼠心臟組織中，HF- Ⅴ-15 能使 ouabain 誘發的心律不整，恢復為正常的跳動。 3、HF- Ⅴ-15 (30μM) 不影響 isoproterenol 的劑量反應曲線。 4、在大白鼠 心室細胞，10μM HF-Ⅴ-15 會延長動作電位，但不影響零期去極化速率 ，在 30μM 會使膜電位去極化，動作電位期間更加延長，並且顯著抑制 零期去極化速率。 5、利用全細胞膜電位鉗定法，HF-Ⅴ-15 (3∼100μ M) 會抑制鈉電流，使鈉電流穩定不活化曲線向負電位方向漂移，並使鈉
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Niemetz, Markus [Verfasser]. "Chelatliganden mit 1-(Pyridin-2-yl)ethylamin als chiralem Baustein / vorgelegt von Markus Niemetz." 2001. http://d-nb.info/962784028/34.

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Wang, Ming-Hsin, and 王銘新. "Effects of Capsaicin and Its Derivative-CAPCNC2(N[Ethylamino-(4-oxymethylene,5-methylene-3-methoxybenzy1]nonanamide)on Platelet Aggregation and Cardiovascular Function." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/08967446070926254275.

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Book chapters on the topic "Ethylamine"

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Lide, David R. "Ethylamine." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-210.

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Howard, Philip H., Gloria W. Sage, William F. Jarvis, and D. Anthony Gray. "Ethylamine." In Handbook of Environmental Fate and Exposure Data For Organic Chemicals, Volume II. CRC Press, 2023. http://dx.doi.org/10.1201/9781003418863-35.

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Wohlfarth, Christian. "Viscosity of ethylamine." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_48.

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Holze, Rudolf. "Ionic conductivities of ethylamine." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_124.

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Holze, Rudolf. "Ionic conductance of ethylamine hydrochloride." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_441.

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Wohlfarth, Christian. "Static dielectric constant of ethylamine." In Static Dielectric Constants of Pure Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-48168-4_27.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) chloro complex with 2-(benzylthio)-ethylamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_359.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) nitrato complex with 2-(benzylthio)ethylamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_360.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) thiocyanato complex with 2-(benzylthio)ethylamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_361.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) iodo complex with 2-(benzylthio)ethylamine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_362.

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Conference papers on the topic "Ethylamine"

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Adan, Dalina, Bohari Yamin, Ong Wei Leng, and Nazlina Ibrahim. "Synthesis, characterization and antibacterial study of tripodal tris-(N-benzoylthioureido)ethylamine." In THE 2014 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2014 Postgraduate Colloquium. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4895199.

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Sherlin, Y. Sheeba, T. Vijayakumar, S. D. D. Roy, and V. S. Jayakumar. "Molecular docking and spectroscopic investigations aided by density functional theory of Parkinson’s drug 2-(3,4-dihydroxyphenyl)ethylamine." In PROCEEDINGS OF THE INTERNATIONAL SEMINAR ON METALLURGY AND MATERIALS (ISMM2017): Metallurgy and Advanced Material Technology for Sustainable Development. Author(s), 2018. http://dx.doi.org/10.1063/1.5038720.

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Abaies, Jawad Kadhim, Blqees Raheem Odhafa, Sura Hamid Kathim, Raheem A. H. Al-Uqaily, and Subhi A. H. Al-Bayaty. "Effect of inhibition on low carbon steel corrosion in acidic conditions by 2-(p-tolyl) ethylamine under different conditions." In TRANSPORT, ECOLOGY, SUSTAINABLE DEVELOPMENT: EKO VARNA 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0191597.

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Senan, Ahmed M., Senem Akkoc, and Alariqi Reem. "Modification and Characterization of Lactoferrin-Iron Free with Methylimidazolium N-ethylamine Ionic Liquid as Potential Drugs Anti SARS-CoV-2." In ECP 2023. MDPI, 2023. http://dx.doi.org/10.3390/ecp2023-14701.

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Polgár, J., Y. Hidasi, A. Toth, and L. Muszbek. "MEASUREMENT OF FACTOR XIII ACTIVITY IN HUMAN PLATELET HOMOGENATE BY A NEW UV-KINETIC METHOD." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644647.

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Factor XIII (FXIIl) of blood coagulation is a zymogen which is converted into an active transglutaminase during the clotting process. Earlier methods used for its determination are cumbersome, laborious, and not suitable for routine laboratory measurements.Most recently we have designed a new simple UV-kinetic assay for the determination of FXIII in the plasma (Muszbek et al., Clin. Chem., 3JL, 35, 1985). The assay is performed on def:j.b-rinated plasma in which FXIII is activated by thrombin and Ca2+. Acetylateddephosphorylated (AD)β-casein and ethylamine are used as substrates and the ammoni
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Gobin, C. "High Pressure Spectroscopic Study of the Action of N-Ethylamines and Water on the 2-Nitropropane/Nitric System." In SHOCK COMPRESSION OF CONDENSED MATTER - 2003: Proceedings of the Conference of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2004. http://dx.doi.org/10.1063/1.1780468.

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Reports on the topic "Ethylamine"

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Zagorchev, Plamen, Elisaveta Apostolova, Vesela Kokova, Lyudmil Peychev, Zhivko Peychev, and Milena Draganova-Filipova. Activation of Kv7.2 to Kv7.5 Channels by Retigabine Modulates the Effects of Histamine and 2‑(2‑Pyridyl) Ethylamine on Smooth Muscles. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2018. http://dx.doi.org/10.7546/crabs.2018.10.18.

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Wackett, Lawrence, Raphi Mandelbaum, and Michael Sadowsky. Bacterial Mineralization of Atrazine as a Model for Herbicide Biodegradation: Molecular and Applied Aspects. United States Department of Agriculture, 1999. http://dx.doi.org/10.32747/1999.7695835.bard.

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Atrazine is a broadly used herbicide in agriculture and it was used here as a model to study the biodegradation of herbicides. The bacterium Pseudomonas sp. ADP metabolizes atrazine to carbon dioxide and ammonia and chloride. The genes encoding atrazine catabolism to cyanuric acid were cloned and expressed in Escherichia coli. The genes were designated atzA, atzB and atzC. Each gene was sequenced. The enzyme activities were characterized. AtzA is atrazine chlorohydrolase which takes atrazine to hydroxyatrizine. AtzB is hydroxyatrazine N-ethylaminohydrolase which produces N-isopropylammelide an
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