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Journal articles on the topic 'Organosulfur Amino Acid Derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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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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2

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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4

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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5

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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6

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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8

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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9

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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10

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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11

Tazetdinova, A. A., O. A. Luzina, M. P. Polovinka, N. F. Salakhutdinov, and G. A. Tolstikov. "Amino-derivatives of usninic acid." Chemistry of Natural Compounds 45, no. 6 (2009): 800–804. http://dx.doi.org/10.1007/s10600-010-9502-z.

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12

Krasylov, I. V., V. S. Moskvina, S. V. Shilin, and V. P. Khilya. "Amino-Acid Derivatives of Pyranocoumarins." Chemistry of Natural Compounds 56, no. 5 (2020): 832–36. http://dx.doi.org/10.1007/s10600-020-03163-3.

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13

Clark, Peter D., Nicholas M. Irvine, and Pratibha Sarkar. "The synthesis of 3H-naphthol[1,8-bc]thiophene derivatives." Canadian Journal of Chemistry 69, no. 6 (1991): 1011–16. http://dx.doi.org/10.1139/v91-148.

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Methods for the synthesis of keto derivatives of the little studied naphtho[1,8-bc]thiophene system have been developed. Using the readily available benzothiophene derivative 6,7-dihydrobenzo[b]thiophen-4(5H)-one 4, a 3-keto-naphtho[1,8-bc]thiophene 14 was synthesized by a tin(IV) chloride catalyzed cyclization of the acid chloride derivative of the saturated acid 13b. The bicyclic ketone 4 was also used to prepare the keto-sulfoxide 7, which was cyclized to the 4-keto-naphtho[1,8-bc]thiophene system 9 in a Pummerer-type rearrangement. Key words: synthesis, organosulfur, naphtho[1,8-bc]thiophe

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14

Gunam, Ida Bagus Wayan, Teruo Sone, and Kozo Asano. "Biodesulfurization of the mixture of dibenzothiophene and its alkylated derivatives by Sphingomonas subarctica T7b." Indonesian Journal of Biotechnology 26, no. 3 (2021): 122. http://dx.doi.org/10.22146/ijbiotech.62584.

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Organosulfur compounds classified as dibenzothiophenes (DBTs) and their derivatives are contained in petroleum. When used as fuel, these substances release SOx emissions, thus contributing to air pollution, acid rain, and climate change. Therefore, it is necessary to reduce the content of these organic sulfur compounds in fuels and one way to achieve this is through bacterial desulfurization. This study reports the biodesulfurization process of a mixture of DBT, 4-hexyl DBT, 4,6-dibutyl DBT, and various organosulfur compounds in light gas oil (LGO). The experiment was conducted by treating 1 m

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15

Easton, CJ, EW Tan, and CM Ward. "Synthesis of Cyclopropyl Amino Acid Derivatives." Australian Journal of Chemistry 45, no. 2 (1992): 395. http://dx.doi.org/10.1071/ch9920395.

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Derivatives of α,β-methanovaline, α,β-methanophenylalanine and β-methyl-αβmethanoalanine have been prepared by regioselective side-chain functionalization of suitably protected amino acid derivatives, followed by cyclization with either sodium hydride or 1,8-diazabicyclo[5.4.O]undec-7-ene. The approach used in this work illustrates a method for the synthesis of cyclopropyl amino acid derivatives which is complementary to existing procedures.

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16

Cohen, Steven A., Brian A. Bidlingmeyer, and Thomas L. Tarvin. "PITC derivatives in amino acid analysis." Nature 320, no. 6064 (1986): 769–70. http://dx.doi.org/10.1038/320769a0.

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17

Safadi, Muhammad, Michael Chorev, and Eli Breuer. "Aminoacylphosphonates-Novel Modified Amino Acid Derivatives." Phosphorus, Sulfur, and Silicon and the Related Elements 51, no. 1-4 (1990): 396. http://dx.doi.org/10.1080/10426509008040923.

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18

Safadi, Muhammad, Michael Chorev, and Eli Breuer. "Aminoacylphosphonates - Novel Modified Amino Acid Derivatives." Phosphorus, Sulfur, and Silicon and the Related Elements 51, no. 1 (1990): 396. http://dx.doi.org/10.1080/10426509008544441.

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19

Rzeska, Alicja, Joanna Malicka, Katarzyna Guzow, Mariusz Szabelski, and Wiesław Wiczk. "New highly fluorescent amino-acid derivatives." Journal of Photochemistry and Photobiology A: Chemistry 146, no. 1-2 (2001): 9–18. http://dx.doi.org/10.1016/s1010-6030(01)00591-3.

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20

Barton, Derek H. R., Jean-Pierre Finet, and Jamal Khamsi. "N-phenylation of amino acid derivatives." Tetrahedron Letters 30, no. 8 (1989): 937–40. http://dx.doi.org/10.1016/s0040-4039(00)95284-5.

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21

Kaminský, Jakub, and Frank Jensen. "Conformational Interconversions of Amino Acid Derivatives." Journal of Chemical Theory and Computation 12, no. 2 (2016): 694–705. http://dx.doi.org/10.1021/acs.jctc.5b00911.

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22

Gredičak, M., A. Kolonić, and I. Jerić. "Novel chloroenyne-modified amino acid derivatives." Amino Acids 35, no. 1 (2007): 185–94. http://dx.doi.org/10.1007/s00726-007-0572-6.

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23

Achamlal, S., A. Elachgar, A. El Hallaoui, S. El Hajji, M. L. Roumestant, and Ph Viallefont. "Synthesis of?-triazolyl?-amino acid derivatives." Amino Acids 12, no. 3-4 (1997): 257–63. http://dx.doi.org/10.1007/bf01373006.

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24

Cohen, Steven A., and Daniel J. Strydom. "Amino acid analysis utilizing phenylisothiocyanate derivatives." Analytical Biochemistry 174, no. 1 (1988): 1–16. http://dx.doi.org/10.1016/0003-2697(88)90512-x.

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25

Ashton, Peter R., Rainer Königer, J. Fraser Stoddart, David Alker та Valerie D. Harding. "Amino Acid Derivatives of β-Cyclodextrin". Journal of Organic Chemistry 61, № 3 (1996): 903–8. http://dx.doi.org/10.1021/jo951396d.

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26

CHIBA, TAKUO, JUN-ICHI SAKAKI, and CHIKARA KANEKO. "Studies on Amino Acid Derivatives. VI." YAKUGAKU ZASSHI 106, no. 2 (1986): 154–57. http://dx.doi.org/10.1248/yakushi1947.106.2_154.

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27

PARUSZEWSKI, Ryszard, Marzanna STRUPINSKA, James P. STABLES, et al. "Amino Acid Derivatives with Anticonvulsant Activity." CHEMICAL & PHARMACEUTICAL BULLETIN 49, no. 5 (2001): 629–31. http://dx.doi.org/10.1248/cpb.49.629.

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28

Débieux, Jean-Luc, and Christian G. Bochet. "Preparation of Photoactivable Amino Acid Derivatives." Journal of Organic Chemistry 74, no. 12 (2009): 4519–24. http://dx.doi.org/10.1021/jo900442p.

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29

Dyker, Gerald. "Amino Acid Derivatives by Multicomponent Reactions." Angewandte Chemie International Edition in English 36, no. 16 (1997): 1700–1702. http://dx.doi.org/10.1002/anie.199717001.

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30

de Zoete, M. C., A. A. Ouwehand, F. van Rantwijk, and R. A. Sheldon. "Enzymatic ammoniolysis of amino acid derivatives." Recueil des Travaux Chimiques des Pays-Bas 114, no. 4-5 (2010): 171–74. http://dx.doi.org/10.1002/recl.19951140408.

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31

Ibrahem, Ismail, Henrik Sundén, Pawel Dziedzic, Ramon Rios, and Armando Córdova. "Asymmetric Amplification in the Amino Acid-Catalyzed Synthesis of Amino Acid Derivatives." Advanced Synthesis & Catalysis 349, no. 11-12 (2007): 1868–72. http://dx.doi.org/10.1002/adsc.200700110.

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32

Ibrahem, Ismail, Henrik Sundén, Pawel Dziedzic, Ramon Rios, and Armando Córdova. "Asymmetric Amplification in the Amino Acid-Catalyzed Synthesis of Amino Acid Derivatives." Advanced Synthesis & Catalysis 350, no. 1 (2008): 9. http://dx.doi.org/10.1002/adsc.200890003.

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33

Muttaqin, Fauzan Zein, Taufik Muhammad Fakih, and Hubbi Nashrullah Muhammad. "MOLECULAR DOCKING, MOLECULAR DYNAMICS, AND IN SILICO TOXICITY PREDICTION STUDIES OF COUMARIN, N-OXALYLGLYCINE, ORGANOSELENIUM, ORGANOSULFUR, AND PYRIDINE DERIVATIVES AS HISTONE LYSINE DEMETHYLASE INHIBITORS." Asian Journal of Pharmaceutical and Clinical Research 10, no. 12 (2017): 212. http://dx.doi.org/10.22159/ajpcr.2017.v10i12.19348.

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Objective: Prostate cancer is the second most common cancer in men. One of the efforts in the treatment of prostate cancer is by inhibiting histone lysine demethylase. Derivative compounds of coumarine, N-oxalylglycine, organoselenium, organosulfur, and pyridine have been reported to be active against two types of histone lysine demethylase (KDM) enzymes, KDM4E and KDM5B. This study aims to study the interactions of these derivatives with KDM.Methods: In this study, we performed computational studies, including molecular docking and molecular dynamics (MDs) simulations, and toxicity prediction

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34

Karavay, P. A., L. I. Nefyodov, and N. L. Karavay. "Amino Acid Imbalance in Atherosclerosis." International Journal of Nutrition 5, no. 2 (2020): 15–23. http://dx.doi.org/10.14302/issn.2379-7835.ijn-20-3188.

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35

Amer, Atef. "SYNTHESIS OF NEW NICOTINOYL AMINO ACID DERIVATIVES." Zagazig Journal of Pharmaceutical Sciences 3, no. 2 (1994): 113–18. http://dx.doi.org/10.21608/zjps.1994.186485.

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36

Esbolaev, E. O., L. A. Aleksandrova, K. A. Toibaeva, and N. A. Aitkhozhina. "C-10 amino acid derivatives of colchicine." Chemistry of Natural Compounds 28, no. 3-4 (1992): 325–28. http://dx.doi.org/10.1007/bf00630252.

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37

Sammakia, T., та G. Notte. "Kinetic Resolution of α-Amino Acid Derivatives". Synfacts 2006, № 5 (2006): 0510. http://dx.doi.org/10.1055/s-2006-934446.

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38

Gallo, August A., Yuxin Liang, and Frederick H. Walters. "Volatile BSTFA Derivatives of Amino Acid Hydroxamates." Analytical Letters 28, no. 4 (1995): 697–701. http://dx.doi.org/10.1080/00032719508001128.

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39

D’Arrigo, Paola, Dario Arosio, Lorenzo Cerioli, et al. "Base catalyzed racemization of amino acid derivatives." Tetrahedron: Asymmetry 22, no. 8 (2011): 851–56. http://dx.doi.org/10.1016/j.tetasy.2011.05.005.

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40

Veselovskaya, M. V., M. M. Garazd, A. S. Ogorodniichuk, Ya L. Garazd, and V. P. Khilya. "Synthesis of amino-acid derivatives of chrysin." Chemistry of Natural Compounds 44, no. 6 (2008): 704–11. http://dx.doi.org/10.1007/s10600-009-9194-4.

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41

Vol'pin, M. E., Z. N. Parnes, and V. S. Romanova. "Amino acid and peptide derivatives of fullerene." Russian Chemical Bulletin 47, no. 5 (1998): 1021–25. http://dx.doi.org/10.1007/bf02498177.

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42

Hubbs, Jed L., Hua Zhou, Astrid M. Kral, et al. "Amino acid derivatives as histone deacetylase inhibitors." Bioorganic & Medicinal Chemistry Letters 18, no. 1 (2008): 34–38. http://dx.doi.org/10.1016/j.bmcl.2007.11.017.

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43

Janůšová, Barbora, Barbora Školová, Katarína Tükörová, et al. "Amino acid derivatives as transdermal permeation enhancers." Journal of Controlled Release 165, no. 2 (2013): 91–100. http://dx.doi.org/10.1016/j.jconrel.2012.11.003.

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44

Juyal, Priyanka, and O. N. Anand. "AMINO ACID DERIVATIVES AS NOVEL FUEL STABILIZERS." Petroleum Science and Technology 20, no. 9-10 (2002): 1009–23. http://dx.doi.org/10.1081/lft-120003694.

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45

Pernía, Glen J., Jeremy D. Kilburn, and Michael Rowley. "A novel receptor for amino acid derivatives." J. Chem. Soc., Chem. Commun., no. 3 (1995): 305–6. http://dx.doi.org/10.1039/c39950000305.

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46

Serkov, I. V., E. A. Chugunova, A. R. Burilov, and S. O. Bachurin. "Synthesis of amino acid derivatives of benzofuroxan." Doklady Chemistry 450, no. 2 (2013): 149–51. http://dx.doi.org/10.1134/s0012500813060013.

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47

TANASE, Reiko, Rio SENDA, Yuna MATSUNAGA, and Masataka NARUKAWA. "Taste Characteristics of Various Amino Acid Derivatives." Journal of Nutritional Science and Vitaminology 68, no. 5 (2022): 475–80. http://dx.doi.org/10.3177/jnsv.68.475.

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48

Kochetkov, K. A., Zh S. Urmambetova, V. M. Belikov, and Z. B. Bakasova. "Higher N-acyl-L-amino acid derivatives." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 39, no. 11 (1990): 2311–16. http://dx.doi.org/10.1007/bf00958844.

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49

Abdalla, S., E. Bayer, and H. Frank. "Derivatives for separation of amino acid enantiomers." Chromatographia 23, no. 2 (1987): 83–85. http://dx.doi.org/10.1007/bf02312877.

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50

Nai-Xing, Wang, Li Ji-Sheng, and Zhu Dao-Ben. "Reaction of amino acid derivatives with C60." Chinese Journal of Chemistry 14, no. 2 (2010): 167–70. http://dx.doi.org/10.1002/cjoc.19960140212.

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