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Relevant bibliographies by topics / Organosulfur Amino Acid Derivatives

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Academic literature on the topic 'Organosulfur Amino Acid Derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Organosulfur Amino Acid Derivatives"

1

RAGAB, A. EL-SAYED. "Some Novel Organosulfur Amino Acid Derivatives." Journal of Indian Chemical Society Vol. 75, May 1998 (1998): 323–24. https://doi.org/10.5281/zenodo.5945267.

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Chemistry Department. Faculty of Science, Al-Azhar University, Nasr City,Cairo, Egypt <em>Manuscript received 14 February 1997, accepted 8 September 1997</em> Synthesis of a series of 4-chlorocinnamanilide-4'-sulfonylamino acids (2-8), and some of the corresponding amino acid methyl esters (9-13) and hydrazides (14-16) are described. Coupling reactions of 4-chlorocinnamanilidc-4'-sulfonylamino acids with amino acid methyl ester hydrochloride in <strong>THF-Et<sub>3</sub>N</strong> medium using dicyclohexylcarbidiimide method give the dipeptide methyl esters (17-19).

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El-Sayed, Ragab A. "ChemInform Abstract: Some Novel Organosulfur Amino Acid Derivatives." ChemInform 30, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199944213.

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3

Praveen, Reddy P., and Rao V. Uma Maheswara. "Effect of nutrient and physical parameters on dibenzothiophene desulfurization activity of Streptomyces sp. VUR PPR 101 isolated from oil contaminated soils of mechanical workshops." Research Journal of Chemistry and Environment 26, no. 6 (2022): 86–99. http://dx.doi.org/10.25303/2606rjce086099.

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Motor vehicles use petroleum products and release sulfur dioxide gas which causes deleterious effects to environment and humans. The sulfur containing compounds present in petroleum products especially organosulfur compounds serve as major source of sulfur dioxide emission. During refining process, petroleum products are subjected to hydrodesulfurization for the removal of sulfur, which is not an efficient method and most of the organosulfur compounds are not eliminated particularly dibenzothiophene and its derivatives. A process known as biodesulfurization which employs microorganisms was sug

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El-Sayed, Ragab A. "Novel Communication: Some Novel Organosulfur Amino Acid Derivatives as Potential Antiparasitic Agents." Phosphorus, Sulfur, and Silicon and the Related Elements 182, no. 5 (2007): 1143–51. http://dx.doi.org/10.1080/10426500601142221.

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Reddy, P. Praveen, and V. UmaMaheswara Rao. "In Silico dszC Gene Analysis, Modeling and Validation of Dibenzothiophene monooxygenase (DszC Enzyme) of Dibenzothiophene Desulfurizing Streptomyces sp.VUR PPR 102." Biosciences Biotechnology Research Asia 20, no. 3 (2023): 935–43. http://dx.doi.org/10.13005/bbra/3144.

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Human beings are heavily dependent on fossil fuels like coal and petroleum products for various daily activities in life. The large-scale usage of petroleum products releases different types of hazardous gasses, sulfur dioxide being one of them. The oxidation of organosulfur compounds in fuels release sulfur dioxide which is deleterious to humans and one of the causative factors for acid rains. The hydrodesulfurization, a conventional process is practiced for the elimination of sulfur from petroleum products during refining is not up to the mark for the total removal of sulfur content. Especia

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Dibwe, Dya Fita, Saki Oba, Satomi Monde, and Shu-Ping Hui. "Inhibition of Accumulation of Neutral Lipids and Their Hydroperoxide Species in Hepatocytes by Bioactive Allium sativum Extract." Antioxidants 13, no. 11 (2024): 1310. http://dx.doi.org/10.3390/antiox13111310.

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Our ongoing research suggests that extracts from plant-based foods inhibit the accumulation of lipid droplets (LDs) and oxidized lipid droplets (oxLDs) in liver cells. These findings suggest their potential use in the alleviation of metabolic dysfunction-associated fatty liver disease (MAFLD) and its most severe manifestation, metabolic dysfunction-associated steatohepatitis (MASH). Allium extracts (ALs: AL1–AL9) were used to assess their ability to reduce lipid droplet accumulation (LDA) and oxidized lipid droplet accumulation (oxLDA) by inhibiting neutral lipid accumulation and oxidation in

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7

Hudlikar, Rasika R., Davit Sargsyan, David Cheng, et al. "Tobacco carcinogen 4-[methyl(nitroso)amino]-1-(3-pyridinyl)-1-butanone (NNK) drives metabolic rewiring and epigenetic reprograming in A/J mice lung cancer model and prevention with diallyl sulphide (DAS)." Carcinogenesis 43, no. 2 (2021): 140–49. http://dx.doi.org/10.1093/carcin/bgab119.

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Abstract Early detection of biomarkers in lung cancer is one of the best preventive strategies. Although many attempts have been made to understand the early events of lung carcinogenesis including cigarette smoking (CS) induced lung carcinogenesis, the integrative metabolomics and next-generation sequencing approaches are lacking. In this study, we treated the female A/J mice with CS carcinogen 4-[methyl(nitroso)amino]-1-(3-pyridinyl)-1-butanone (NNK) and naturally occurring organosulphur compound, diallyl sulphide (DAS) for 2 and 4 weeks after NNK injection and examined the metabolomic and D

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Mulder, Ines, Torsten Krause, Tobias Sattler, et al. "Thermolytic degradation of methylmethionine and implications for its role in DMS and MeCl formation in hypersaline environments." Environmental Chemistry 12, no. 4 (2015): 415. http://dx.doi.org/10.1071/en14207.

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Environmental context Methyl chloride and dimethyl sulfide are important atmospheric trace gases, but their biogeochemical contributions to the atmosphere are not fully understood. The amino acid derivative methyl methionine has been hypothesised to be a precursor of these two atmospheric gases, especially in drying salt-lake environments. We found methyl chloride and dimethyl sulfide in salt crystals and soil samples of hypersaline lakes, suggesting that a thermal decay of methyl methionine could be one of the formation mechanisms responsible. Abstract Volatile organic halocarbons (VOXs) and

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Doddipatla, Srinivas, Chao He, Ralf I. Kaiser, et al. "A chemical dynamics study on the gas phase formation of thioformaldehyde (H2CS) and its thiohydroxycarbene isomer (HCSH)." Proceedings of the National Academy of Sciences 117, no. 37 (2020): 22712–19. http://dx.doi.org/10.1073/pnas.2004881117.

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Complex organosulfur molecules are ubiquitous in interstellar molecular clouds, but their fundamental formation mechanisms have remained largely elusive. These processes are of critical importance in initiating a series of elementary chemical reactions, leading eventually to organosulfur molecules—among them potential precursors to iron-sulfide grains and to astrobiologically important molecules, such as the amino acid cysteine. Here, we reveal through laboratory experiments, electronic-structure theory, quasi-classical trajectory studies, and astrochemical modeling that the organosulfur chemi

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Park, Kyung-Ho, and Mark J. Kurth. "Cyclic amino acid derivatives." Tetrahedron 58, no. 43 (2002): 8629–59. http://dx.doi.org/10.1016/s0040-4020(02)00989-4.

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Dissertations / Theses on the topic "Organosulfur Amino Acid Derivatives"

1

Peters, Steven Carlton. "Crosslinked amino acid derivatives." Title page, table of contents and abstract only, 1991. http://web4.library.adelaide.edu.au/theses/09PH/09php4831.pdf.

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Van, Kralingen Leon. "Controlled polymerization of amino acid derivatives." Thesis, Link to the Internet, 2008. https://etd.sun.ac.za/jspui/handle/10019/919.

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Kociuba, Katherine. "Radical functionalisation of amino acid derivatives /." Title page, table of contents and abstract only, 1996. http://web4.library.adelaide.edu.au/theses/09PH/09phk76.pdf.

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Tan, Eng Wui. "Regioselective modification of amino acid derivatives /." Title page, contents and abstract only, 1990. http://web4.library.adelaide.edu.au/theses/09PH/09pht1612.pdf.

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Goubet, D. C. M. "Asymmetric synthesis of α-amino acid derivatives". Thesis, Swansea University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637081.

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A general background to α-amino acids is discussed in the first chapter. After a brief account on classification, properties and applications of these compounds, asymmetric processes leading to optically enriched residues are reviewed in detail. The second chapter describes the envisaged stereoselective approach towards these substrates involving Michael-type addition onto a chiral didehydroalanine derivative. Syntheses of α,β-unsaturated amino acids are reviewed after a brief section on Michael-type reactions. The preparation of a chiral didehydroamino acid residue has been investigated using

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Hay, M. P. "Atom transfer reactions of amino acid derivatives." Thesis, University of Canterbury. Chemistry, 1987. http://hdl.handle.net/10092/7974.

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Investigations of atom transfer reactions of amino acid derivatives are described in this thesis. Reaction of N-benzoylvaline methyl ester (29a) with sulphuryl chloride gave the β-chlorovaline derivative (30a) and lesser amounts of diastereoisomers of the r-chlorovaline derivative (31a). Studies of reactions of the valine derivatives (29a-c) with sulphuryl chloride, and of the photolyses of the corresponding N-chlorovaline derivatives (39a-c) have shown that the reaction of (29a) with sulphuryl chloride and the photolysis of (39a) involve regioselective intermolecular transfer of the respectiv

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Masesane, Ishmael Baperi. "Stereoselective routes to cyclic β-amino acid derivatives". Thesis, Durham University, 2003. http://etheses.dur.ac.uk/3700/.

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The literature structure of the natural product oryzoxymycin and an array of 3-mono-,3,4-di- and 3,4,5-tri-hydroxylated derivatives of 2-aminocyclohexane-l-carboxyhc acid (ACHC) were stereoselectively prepared from oxanorbomene adducts derived from the Diels Alder reaction of ethyl (E)-3-nitroacrylate and furan. The central reaction for these syntheses was the base mediated β-elimination of the oxygen bridge of the oxanorbomene adducts or their derivatives. The asymmetnc synthesis of the literature structure of oryzoxymycin involved chiral HPLC or enzyme catalysed kinetic resolution of the end

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Smith, David John. "Complexation of amino-acid derivatives using macrocyclic receptors." Thesis, University of Bath, 1996. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319219.

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Ng, S. C. "Enzymatic and non enzymatic synthesis of amino acid derivatives." Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379948.

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10

Kausar, Nighat. "Experimental spectroscopic and theoretical studies of amino acid derivatives." Thesis, University of Greenwich, 2008. http://gala.gre.ac.uk/6207/.

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Experimental vibrational/electronic circular dichroism spectroscopic and theoretical studies of amino acid derivatives, i.e. N-acetyl-L-Asp, N-acetyl-L-Glu, and di-amino acid peptide/derivatives, i.e. L-Asp-L-Glu, a-N-acetyl-L-Asp-L-Glu, and ß-N-acetyl-L-Asp-L-Glu are reported. The calculated structures for N-acetyl-L-Asp and N-acetyl-L-Glu differ. The conformation of the trans amide moiety changes with the carbon chain length of the side chain of the amino acid derivatives. In the computed structures of N-acetyl-L-Asp and N-acetyl-L-Glu all backbone atoms are in-plane, except the side chain g

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Books on the topic "Organosulfur Amino Acid Derivatives"

1

P, Kukharʹ V., ed. Aminophosphonic and aminophosphinic acids: Chemistry and biological activity. Wiley, 2000.

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2

Regan, Teresa Elizabeth. A study of enzyme-ligand binding of chymotrypsin with amino acid derivatives using infrared spectroscopy. University of Birmingham, 1997.

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3

Victor, Brantl, Teschemacher Hansjörg, and International Symposium on [Beta]-Casomorphins and Related Peptides (2nd : 1991 : Titisee, Germany), eds. [Beta]-casomorphins and related peptides: Recent developments. VCH, 1994.

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4

Amino acid derivatives: A practical approach. Oxford University Press, 1999.

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5

Barrett, Graham C. Amino Acid Derivatives: A Practical Approach (Practical Approach Series). Oxford University Press, USA, 2000.

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6

Allosteric modulation of amino acid receptors: Therapeutic implications. Raven Press, 1989.

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7

Fisher, Melvin Philip. Synthesis of Some N-Substituted Alpha-amino-alpha-phenylacetic Acid Ester Derivatives. Creative Media Partners, LLC, 2021.

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8

Mistry, Mala. Studies towards the synthesis of novel alpha-amino acid derivatives using dynamic kinetic resolution methods. 2004.

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9

Chen, Yu. Applications of partially fluorinated binaphthol ligands in asymmetric catalysis and synthesis of alpha-amino acid derivatives. 2005.

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10

Barnard, E. A. Allosteric Modulation of Amino Acid Receptors: Therapeutic Implications (Fidia Research Symposium Series, Vol 1). Raven Pr, 1989.

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Book chapters on the topic "Organosulfur Amino Acid Derivatives"

1

Brückner, Hans, Barbara Sorsche, Ali Esna-Ashari, and Rolf Jöster. "Chiral ligand-exchange chromatography of amino acid derivatives." In Amino Acids. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_18.

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2

Monteiro, Luís S., and Fátima Paiva-Martins. "Amino Acids, Amino Acid Derivatives and Peptides as Antioxidants." In Lipid Oxidation in Food and Biological Systems. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-87222-9_17.

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3

Stock, J. A. "Amino Acid and Peptide Derivatives with Potential Antitumour Properties." In Ciba Foundation Symposium - Amino Acids and Peptides with Antimetabolic Activity. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719114.ch7.

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4

Boyajyan, A., A. Poghosyan, T. Hovsepyan, et al. "Cyclic Amino Acid Derivatives as New Generation of Radioprotectors." In NATO Science for Peace and Security Series B: Physics and Biophysics. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7003-4_24.

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5

Friedman, Mendel, and Carol E. Levin. "Nutritional Value of d-Amino Acids, d-Peptides, and Amino Acid Derivatives in Mice." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-331-8_23.

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6

Juaristi, Eusebio, Víctor Manuel Gutiérrez-García та Heraclio López-Ruiz. "Enantioselective Synthesis of β-Amino Acids via Stereoselective Hydrogenation of β-Aminoacrylic Acid Derivatives". У Enantioselective Synthesis of β-Amino Acids. John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471698482.ch7.

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7

Spasova, Maya, Stefan Philipov, and Tsenka Milkova. "Amino acid Derivatives of Aporphinic Alkaloid Glaucine and their antioxidant activity." In Advances in Experimental Medicine and Biology. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-73657-0_120.

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8

Bergman, Tomas, Mats Carlquist, and Hans Jörnvall. "Amino Acid Analysis by High Performance Liquid Chromatography of Phenylthiocarbamyl Derivatives." In Advanced Methods in Protein Microsequence Analysis. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71534-1_5.

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9

Tsugita, A., and M. Kamo. "Sensitive Determination of Amino Acid Derivatives from N-Terminal Sequence Analysis." In Methods in Protein Sequence Analysis. Birkhäuser Basel, 1991. http://dx.doi.org/10.1007/978-3-0348-5678-2_11.

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10

Akazome, Motohiro. "Chiral Recognition by Inclusion Crystals of Amino-Acid Derivatives Having Trityl Groups." In Advances in Organic Crystal Chemistry. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-55555-1_23.

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Conference papers on the topic "Organosulfur Amino Acid Derivatives"

1

Deebb, Samara, and Mohammad Sadakaa. "Synthesis of New Amino Acid-Conjugated Derivatives of a Sulphonamide." In 5th International Conference on Biomedical and Health Sciences. Cihan University-Erbil, 2024. http://dx.doi.org/10.24086/biohs2024/paper.1270.

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The subsequent synthesis involved the preparation of novel sulfonamide derivatives from 4-acetamidobenzenesulfanyl chloride. 4-acetamidobenzenesulfanyl chloride was synthesized as the initial compound, followed by the preparation of derivatives through the reaction of 4-acetamidobenzenesulfanyl with the amino acids valine, alanine, and tryptophan using a basic solution of sodium hydroxide. The structures of the derivatives determined by the using FT-IR, 1 H-NMR, 13C-NMR, and DEPT 135o analysis. In addition, the derivatives were also evaluated for their antimicrobial effectiveness against signi

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2

Fakhar, Imran, Bohari M. Yamin, and Siti Aishah Hasbullah. "Synthesis and characterization of bis-thiourea having amino acid derivatives." In THE 2016 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2016 Postgraduate Colloquium. Author(s), 2016. http://dx.doi.org/10.1063/1.4966750.

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Kawabata, Takeo, Hideo Suzuki, Yoshikazu Nagae, Thomas Wirth, Kyoshi Yahiro, and Kaoru Fuji. "Memory of Chirality in Alkylation of a-Amino Acid Derivatives." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01872.

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Warsito, Warsito, Masruri Masruri, Sinta Murlistyarini, Dwika Putri Pangesti, and Asyfariatus Zulfa Azhar. "Screening Multitarget Anticancer Compounds from Salicylic Acid Derivatives: (Without and with Amino Acid Linkage) by <i>In Silico</i> Docking." In International Conference on Chemistry and Material Sciences 2023 (IC2MS). Trans Tech Publications Ltd, 2024. http://dx.doi.org/10.4028/p-svkm5p.

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This research aims to design anticancer molecules using the hybridization concept based on molecular derivatives of salicylic acid. The investigation explores structures with and without linked amino acid alanine through an in-silico docking approach. The research conducts screenings of the designed salicylic acid derivative molecules against receptors, including MMP9, MMP2, CDK2, P53, BAK EGFR, and ADP Ribose Polymerase. The most promising docking results for multitarget cancer compounds were observed in salicylic acid derivatives with amino acid linkages, specifically salicylic acid-curcumin

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Grueva, Ekaterina S., Tsenka S. Milkova, and Tamara I. Pajpanova. "The design and synthesis of novel N-cholyl amino acid derivatives." In VIIIth Conference Biologically Active Peptides. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2003. http://dx.doi.org/10.1135/css200306032.

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Correia, João D. G., Rúben D. M. Silva, Cristina P. Matos, et al. "Technetium-99m tricarbonyl complexes containing amino acid derivatives for cancer imaging." In 37th European Peptide Symposium. The European Peptide Society, 2024. http://dx.doi.org/10.17952/37eps.2024.p1012.

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Bondareva, N. A., P. P. Purygin, V. A. Ermokhin, A. S. Gilmutdinova, and L. I. Bashirova. "Synthesis of derivatives of aminocaproic acid, taurine and a few amino acids." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069053.

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Nuratikah, Liana Dewi, Bambang Cahyono, and Parsaoran Siahaan. "UV/vis absorption computational studies of azobenzene derivatives ((4-aminomethyl)phenylazobenzoic acid (AMPB)) with amino acid." In THE 9TH INTERNATIONAL CONFERENCE OF THE INDONESIAN CHEMICAL SOCIETY ICICS 2021: Toward a Meaningful Society. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0104176.

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Ruiz, María, Vicente Ojea, M. Fernández, Susanna Conde, Aniana Díaz, and José Quintela. "Stereoselective Synthesis of 2-Amino-2-methyl-4-phosphonobutanoic Acid Derivatives (MAP4 Analogues)." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02020.

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Quintela, J., M. Fernández, V. Ojea, M. Ruiz, S. Conde, and A. Díaz. "Stereoselective Synthesis of 2-Amino-4-phosphono-4-pentenoic Acid Derivatives (AP4 Analogues)." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02021.

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Reports on the topic "Organosulfur Amino Acid Derivatives"

1

Wisniewski, Michael, Samir Droby, John Norelli, Dov Prusky, and Vera Hershkovitz. Genetic and transcriptomic analysis of postharvest decay resistance in Malus sieversii and the identification of pathogenicity effectors in Penicillium expansum. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7597928.bard.

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Use of Lqh2 mutants (produced at TAU) and rNav1.2a mutants (produced at the US side) for identifying receptor site-3: Based on the fact that binding of scorpion alpha-toxins is voltage-dependent, which suggests toxin binding at the mobile voltage-sensing region, we analyzed which of the toxin bioactive domains (Core-domain or NC-domain) interacts with the DIV Gating-module of rNav1.2a. This analysis was based on the assumption that the dissociation of toxin mutants upon depolarization would vary from that of the unmodified toxin should the substitutions affect a site of interaction with the ch

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