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Relevant bibliographies by topics / N-acyl

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Academic literature on the topic 'N-acyl'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "N-acyl"

1

Cerrini, Silvio, Walter Fedeli, Gino Lucente, Fernando Mazza, Francesco Pinnen, and GIancarlo Zanotti. "N-acyl-diketopiperazines." International Journal of Peptide and Protein Research 23, no. 3 (2009): 223–29. http://dx.doi.org/10.1111/j.1399-3011.1984.tb02713.x.

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MAZZA, FERNANDO, GIORGIO POCHETTI, DOMENICO ROSSI, and GINO LUCENTE. "N-Acyl-diketopiperazines." International Journal of Peptide and Protein Research 26, no. 2 (2009): 166–73. http://dx.doi.org/10.1111/j.1399-3011.1985.tb03193.x.

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Zhao, Huanxia, Chengxuan He, Yawen Zhou, Jian Yang, Cong Luo, and Baocai Xu. "Study on foaming properties of N-acyl amino acid surfactants: Sodium N-acyl glycinate and sodium N-acyl phenylalaninate." Colloids and Surfaces A: Physicochemical and Engineering Aspects 567 (April 2019): 240–48. http://dx.doi.org/10.1016/j.colsurfa.2019.01.073.

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Tørring, Thomas, Stephanie R. Shames, Wooyoung Cho, Craig R. Roy, and Jason M. Crawford. "Acyl Histidines: New N-Acyl Amides fromLegionella pneumophila." ChemBioChem 18, no. 7 (2017): 638–46. http://dx.doi.org/10.1002/cbic.201600618.

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Esker, John L., and Martin Newcomb. "Multiple Reaction Channels of (N-Acyl-N-alkylcarbamoyl)oxyl Radicals from N-Acyl PTOC Carbamates." Journal of Organic Chemistry 59, no. 10 (1994): 2779–86. http://dx.doi.org/10.1021/jo00089a023.

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Paik, S. "N-acyl-N-nitrosoamino acids and peptides." Tetrahedron Letters 35, no. 41 (1994): 7731–34. http://dx.doi.org/10.1016/s0040-4039(00)77358-8.

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Paik, Seunguk, and Emil H. White. "N-acyl-N-nitrosoamino acids and peptides." Tetrahedron Letters 35, no. 42 (1994): 7731–34. http://dx.doi.org/10.1016/0040-4039(94)80104-5.

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Van Overloop, Helena, Gerd Van der Hoeven, and Paul P. Van Veldhoven. "N-Acyl migration in ceramides." Journal of Lipid Research 46, no. 4 (2005): 812–16. http://dx.doi.org/10.1194/jlr.d400034-jlr200.

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9

Damon, R. E., and G. M. Coppola. "Cleavage of N-acyl oxazolidones." Tetrahedron Letters 31, no. 20 (1990): 2849–52. http://dx.doi.org/10.1016/0040-4039(90)80164-h.

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10

Beyer, Lothar, Eberhard Hoyer, Jürgen Liebscher, and Horst Hartmann. "Komplexbildung mit N-Acyl-thioharnstoffen." Zeitschrift für Chemie 21, no. 3 (2010): 81–91. http://dx.doi.org/10.1002/zfch.19810210302.

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Dissertations / Theses on the topic "N-acyl"

1

Al-Faiyz, Yasair S. S. "The chemistry of O-acyl derivatives of N-acyl hydroxamic acid." Thesis, University of Warwick, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252534.

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Penman, June. "GPR55 and N-acyl amino acids." Thesis, University of Dundee, 2013. https://discovery.dundee.ac.uk/en/studentTheses/2e07c280-3a61-4f49-a9da-1fa4ffc79fa5.

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G-protein coupled receptor 55 (GPR55) is a novel lipid sensing receptor activated by the endogenous lipid, lysophosphatidylinositol (LPI) and is reported as a putative cannabinoid receptor. However GPR55 shares limited homology with the two cloned cannabinoid receptors (CB<sub>1</sub> and CB<sub>2</sub>) but does exhibit some cannabinoid sensitivity. Recently a family of bioactive lipids, the N-acyl amino acids, are gaining interest due to their structural similarity to endocannabinoids (naturally occurring CB<sub>1</sub> and CB<sub>2</sub> agonists). N-acyl amino acids have little or no affin

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3

Wang, Xueqing. "Oxidative cyclization of phenolic N-acyl sulfonamides." Thesis, University of British Columbia, 2017. http://hdl.handle.net/2429/61303.

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The oxidative activation of appropriately substituted phenols with a hypervalent iodine reagent, in the presence of suitable nitrogen nucleophiles, results in formation of 2- or 4-amidodienones. The process is described as the oxidative amidation of phenols. The dienones thus produced are useful building blocks for the synthesis of alkaloids. The nitrogen nucleophile may be an oxazoline, a sulfonamide or phosphoramide (intramolecular reactions), or a nitrile (bimolecular reaction), but not a carboxamide. This is because carboxamides express Onucleophilicity toward oxidatively activated phenols

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4

Wilkinson, Adam. "N-acyl-homoserine lactone signalling in Rhizobium leguminosarum." Thesis, University of East Anglia, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267721.

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5

Simpson, Mark Geoffrey. "Steroid and heterocycle-based macrocyclic N-Acyl hydrazones." Thesis, University of Cambridge, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.621549.

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Jones, Faye-Ellen. "Inhibition of N-acyl-homoserine lactone quorum sensing." Thesis, University of Aberdeen, 2000. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU602017.

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Quorum-sensing amongst Gram-negative bacteria is an important method of intercellular communication required for conveying information about population density. The extracellular accumulation of the signal molecule involved, N-acyl homoserine lactone (AHL), leading to increases in internal physiological concentration, allows phenotypic switching to occur that is beneficial to the bacterial population. In our laboratory, analysis of the effect of AHL on phenotype currently involves creating null mutants unable to produce AHL, then reintroducing the signal molecule exogenously. With the increasi

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Azzaro, Stéphane. "Réactivités radicalaire et organométallique des N-acyl-sulfonimidamides." Paris 6, 2009. http://www.theses.fr/2009PA066331.

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Waluk, Dominik Paweł. "Biosynthesis and physiological functions of N-acyl amino acids." Doctoral thesis, Stockholms universitet, Institutionen för genetik, mikrobiologi och toxikologi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-75766.

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N-acyl amino acids are lipid signalling molecules that have recently been identified in biological systems. These lipids are structurally related to the endocannabinoids, although they do not activate cannabinoid receptors. In 2001, N-arachidonoyl glycine was the first signalling lipid in this group to be identified in bovine and rat brain and since then, about 50 novel N-acyl amino acids have been identified in mammalian systems. These N-acyl amino acids are involved in regulating pain processes, are anti-inflammatory and regulate body temperature, but the metabolic pathways for production an

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Wells, Greggory M. "Synthesis and Biological Activity of N-Acyl Aziridines." Ohio University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1450458169.

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Markey, Michael D. "Synthesis of cribrostatin 6, santiagonamine, and a N-acyl pyridinium salt." Thesis, Boston College, 2008. http://hdl.handle.net/2345/1358.

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Books on the topic "N-acyl"

1

Al-Faiyz, Yasair S. S. The chemistry of O-acyl derivatives of N-acyl hydroxamic acid. typescript, 2002.

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2

Kumpf, Siegfried. Diastereoselektive heterogene katalytische Hydrierungen von N'-Acyl-[alpha],[beta]-Didehydrodipeptiden [N'-Acyl-alpha,beta-Didehydrodipeptiden]. [s.n.], 1992.

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3

Linoh, Karin. Synthetische und strukturelle Untersuchungen über Dimesylamin-Derivate: N-Acyl-dimesylamine, [gamma]-Dimesylamino-D[beta],[gamma]-butenolid, Salze des Dimesylamins mit N-Acylonium- sowie einfachen und komplexen d-Metall-Kationen, [18-Krone-6]₃[Dimesylamin]₂. [s.n.], 1989.

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4

Sencherey, Bernard Baffour. Photochemical generation and reactions of N-acyl-1-aza-1,3-diene. 1986.

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5

Bongartz, Claudia. Untersuchungen zum Mechanismus der Wirkung von N-Acyl-Isonicotinsäurehydrazid (INH)-Derivaten auf INH-sensible und -resistente Mycobacterium tuberculosis. 1999.

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6

Zürich, Eidgenössische Technische Hochschule, ed. Versuche zur Herstellung eines N-Acyl-1-aminosulfonamids: Herstellung von enantiomerenreinen Dipeptidderivaten mit einer Phosphonat- anstelle der C-terminalen Carboxylat-Gruppe durch zweifache Peptidmodifikation. 1991.

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7

Priknant, Warawudh. Synthesis and reactivity of polymer-supported n-butyl tin oxide as an acyl-transfer catalyst and synthesis and reactivity of polymer-supported diorgano tin o-neopentyl dithiocarbonates in free radical syntheses. 1996.

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Book chapters on the topic "N-acyl"

1

Schomburg, Dietmar, and Dörte Stephan. "Acyl-[acyl-carrier-protein]-UDP-N-acetylglucosamine O-acyltransferase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_259.

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2

Schomburg, Dietmar, and Dörte Stephan. "N-(Long-chain-acyl)ethanolamine deacylase." In Enzyme Handbook 16. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-58903-4_105.

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3

Schomburg, Dietmar, and Ida Schomburg. "UDP-3-O-acyl-N-acetylglucosamine deacetylase 3.5.1.108." In Class 3.4–6 Hydrolases, Lyases, Isomerases, Ligases. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36260-6_19.

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4

Röhrig, Horst, Jürgen Schmidt, Ursula Wieneke, Richard Walden, Jeff Schell, and Michael John. "N-Acyl Galactosamine Inhibition of Lipo- Chitooligosaccharide Action." In Biological Fixation of Nitrogen for Ecology and Sustainable Agriculture. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59112-9_12.

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5

Christensen, Louise Dahl, Maria van Gennip, Tim Holm Jakobsen, Michael Givskov, and Thomas Bjarnsholt. "Imaging N-Acyl Homoserine Lactone Quorum Sensing In Vivo." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-971-0_11.

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6

Hultqvist, Louise Dahl, Maria Alhede, Tim Holm Jakobsen, Michael Givskov, and Thomas Bjarnsholt. "Imaging N-Acyl Homoserine Lactone Quorum Sensing In Vivo." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7309-5_16.

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7

Flegelová, Z., V. Krchnák, N. F. Sepetov, et al. "Libraries of small compact structures based on N-acyl-N-alkylamino acids." In Peptides 1994. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_211.

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8

Zhang, Changhe, and David Lupton. "N-Heterocyclic Carbene Catalysis via the α,β-Unsaturated Acyl Azolium." In N-Heterocyclic Carbenes in Organocatalysis. Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527809042.ch6.

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9

Ferluga, Sara, Laura Steindler, and Vittorio Venturi. "N-Acyl Homoserine Lactone Quorum Sensing in Gram-Negative Rhizobacteria." In Secondary Metabolites in Soil Ecology. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-74543-3_4.

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10

Paulk Tierney, Aimee R., and Philip N. Rather. "Methods for Detecting N-Acyl Homoserine Lactone Production in Acinetobacter baumannii." In Methods in Molecular Biology. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9118-1_23.

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Conference papers on the topic "N-acyl"

1

Kulik, Katarzyna, Renata Kaczmarek, Ewa Radzikowska, Dariusz Korczyński, Wojciech J. Stec, and Janina Baraniak. "Synthesis of N-acyl phosphoramidate pronucleotides." In XIVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2008. http://dx.doi.org/10.1135/css200810386.

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Jiang, Haizhen, Dehua Tao, and Bin Wang. "Synthesis of the Multifunctional Additive N-acyl Glutamic Acid and Application in Water-Based Lubricating Fluids." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-64205.

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A series of N-acyl glutamic acid were prepared by reaction of glutamic acid with chlorides (1–3) or anhydrides (4–8) in good yield, within the solution of pH 8–10, keeping the reaction at 10∼15°C for 2–3 hours. The tribological behaviors of the resulting N-acyl glutamic acid salts with triethanolamine as additives in water were examined on a four-ball machine. The rust-inhibiting properties were evaluated. The elemental composition of the boundary lubricating film was analyzed by means of auger electron spectroscopy (AES). It was found that the N-acyl glutamic acid with long acyl chain functio

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3

El Rayes, Samir M., M. A. Saad, D. A. Ismail, E. A. Soliman, and M. M. A. EL-Sukkary. "Synthesis and Properties of some N-acyl ethylenediamine triacetic acid Chelating Surfactants." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00489.

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4

Funeng, Tan, Zhang Zhixin, Zhou Yunbo, and Sui Weiping. "Preparation and Aggregate Formation of O-Hydroxypropyl-N-Laurel Acyl Chitosan Ramification." In 5th International Symposium on Knowledge Acquisition and Modeling (KAM 2015). Atlantis Press, 2015. http://dx.doi.org/10.2991/kam-15.2015.63.

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Branković, Jovica, Zorica D. Petrović, and Vladimir P. Petrović. "Phenolic N-acyl hydrazone derivatives: In silico assessment of potential antibacterial activity against selected G+ and G- strains." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.491b.

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In this work, a series of phenolic N-acyl hydrazones was investigated in silico against six selected E. coli and S. aureus bacterial proteins. Generally, the obtained molecular docking results revealed significantly higher binding affinities of analogs a–n towards selected enzymes in comparison to standard compounds. In the case of E. coli proteins 1hnj, 1c14, and 6ntw, the lowest binding energies were calculated for derivatives l (-8.5 kcal/mol), d (-9.0 kcal/mol), and k (-8.2 kcal/mol), respectively. On the other hand, the highest binding affinity towards the S. aureus 3u2d, 1mwu, and 1jij e

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6

Sakamoto, Ken, Kohei Sato, Akira Shigenaga, Daisuke Tsuji, Kohji Itoh, and Akira Otaka. "Development of Efficient Synthetic Method for N-Amino Acyl N-Sulfanylethyl Anilide Linkers as Peptide Thioester Equivalent." In The Twenty-Third American and the Sixth International Peptide Symposium. Prompt Scientific Publishing, 2013. http://dx.doi.org/10.17952/23aps.2013.242.

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Branković, Jovica, Zorica D. Petrović, and Vladimir P. Petrović. "In silico antibiofilm potency of phenolic N-acyl hydrazones against selected bacterial strains." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.495b.

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In the present work, fourteen phenolic hydrazone derivatives were evaluated for their in silico inhibitory activity against selected P. aeruginosa and S. maltophilia proteins involved in drug resistance and biofilm formation. Molecular docking analysis revealed the highest binding affinity of analogs n (-8.4 kcal/mol) and h (-7.3 kcal/mol) towards P. aeruginosa 7m1m and 7m1l proteins, respectively. In the case of S. maltophilia, analog k (-8.4 kcal/mol) expressed the highest binding affinity to 6qw7, whereas for 6uaf, the lowest binding energy was calculated for derivative d (-8.1 kcal/mol). T

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8

Vektarienė, Aušra, Gytis Vektaris, and Arvydas Juodviršis. "Substitution Effects on Reactivity of N-Acyl- 2-amino-2-desoxigliukopyranoses. Quantum Chemical Study." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01826.

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9

Vítovcová, Miloslava, Jan Hlaváček, Jan Pícha, Václav Vaněk, Jiří Jiráček, and Václav Kašička. "Capillary electrophoresis applied to analysis and characterization of mono-N-acyl-2,6-diaminopimelic acid derivatives." In XIIth Conference Biologically Active Peptides. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201113159.

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10

Colombani-Garay, Daniel J., and Jetze Tepe. "Development ofN-acyl Fluspirilene 20S Proteasome Enhancers for the Treatment of Neurodegenerative Diseases." In ASPET 2024 Annual Meeting Abstract. American Society for Pharmacology and Experimental Therapeutics, 2024. http://dx.doi.org/10.1124/jpet.295.131514.

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Reports on the topic "N-acyl"

1

Yedidia, I., H. Senderowitz, and A. O. Charkowski. Small molecule cocktails designed to impair virulence targets in soft rot Erwinias. United States-Israel Binational Agricultural Research and Development Fund, 2020. http://dx.doi.org/10.32747/2020.8134165.bard.

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Chemical signaling between beneficial or pathogenic bacteria and plants is a central factor in determining the outcome of plant-microbe interactions. Pectobacterium and Dickeya (soft rot Erwinias) are the major cause of soft rot, stem rot, and blackleg formed on potato and ornamentals, currently with no effective control. Our major aim was to establish and study specific bacterial genes/proteins as targets for anti-virulence compounds, by combining drug design tools and bioinformatics with experimental work. The approach allowed us to identify and test compounds (small molecules) that specific

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2

Ron, Eliora, and Eugene Eugene Nester. Global functional genomics of plant cell transformation by agrobacterium. United States Department of Agriculture, 2009. http://dx.doi.org/10.32747/2009.7695860.bard.

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The aim of this study was to carry out a global functional genomics analysis of plant cell transformation by Agrobacterium in order to define and characterize the physiology of Agrobacterium in the acidic environment of a wounded plant. We planed to study the proteome and transcriptome of Agrobacterium in response to a change in pH, from 7.2 to 5.5 and identify genes and circuits directly involved in this change. Bacteria-plant interactions involve a large number of global regulatory systems, which are essential for protection against new stressful conditions. The interaction of bacteria with

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