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Journal articles on the topic 'Ligands (Biochemistry) Organosulfur compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Takeda, Takeshi, Yasuo Horikawa, Tadahiro Nomura, Mikako Watanabe, Ichiro Miura, and Tooru Fujiwara. "Desulfurizative Titanation of Organosulfur Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 120, no. 1 (1997): 391–92. http://dx.doi.org/10.1080/10426509708545563.

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2

Anisimov, A. V., Zh B. Myltykbaeva, Zh Kairbekov, et al. "Pyridine derivatives as ligands of metal complexes for the peroxidation of organosulfur compounds." Theoretical Foundations of Chemical Engineering 51, no. 4 (2017): 563–66. http://dx.doi.org/10.1134/s0040579517040029.

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3

Block, Eric. "Chemistry of Analogous Organoselenium and Organosulfur Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 172, no. 1 (2001): 1–23. http://dx.doi.org/10.1080/10426500108046637.

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4

Ariga, Toyohiko, Kentaro Tsuji, Taiichiro Seki, Tadaaki Moritomo, and Jun-Ichiro Yamamoto. "Antithrombotic and antineoplastic effects of phyto-organosulfur compounds." BioFactors 13, no. 1-4 (2000): 251–55. http://dx.doi.org/10.1002/biof.5520130138.

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5

Gómez-Paz, Olaya, Rosa Carballo, Ana Belén Lago, and Ezequiel M. Vázquez-López. "Metallosupramolecular Compounds Based on Copper(II/I) Chloride and Two Bis-Tetrazole Organosulfur Ligands." Chemistry 2, no. 1 (2020): 33–49. http://dx.doi.org/10.3390/chemistry2010005.

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The present work assesses the ability of two flexible bis-tetrazole organosulfur ligands to build up different metallosupramolecular compounds based on the analysis of the different supramolecular interactions. The reaction of copper(II) chloride dihydrate with the N,N’-donor dithioether ligands bis(1-methyl-1H-tetrazole-5-ylthio)methane (BMTTM) and 1,2-bis(1-methyl-1H-tetrazole-5-ylthio)ethane (BMTTE) was investigated using different synthetic methods. Four compounds have been obtained as single crystals: two pseudopolymorphic 1D Cu(II) coordination polymers with the ligand BMTTM, a 2D Cu(II)

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6

Avgeri, Ioanna, Konstantina Zeliou, Spyridon A. Petropoulos, Penelope J. Bebeli, Vasileios Papasotiropoulos, and Fotini N. Lamari. "Variability in Bulb Organosulfur Compounds, Sugars, Phenolics, and Pyruvate among Greek Garlic Genotypes: Association with Antioxidant Properties." Antioxidants 9, no. 10 (2020): 967. http://dx.doi.org/10.3390/antiox9100967.

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In order to assess the diversity of Greek garlic (Allium sativum L.) landraces, 34 genotypes including commercial ones were grown in the same field and their content in organosulfur compounds, pyruvate, total sugars, and total phenolics, alongside antioxidant capacity, was determined. The organosulfur compounds were studied by Gas Chromatography–Mass Spectrometry (GC–MS) after ultrasound-assisted extraction in ethyl acetate, identifying 2-vinyl-4H-1,3-dithiin and 3-vinyl-4H-1,2-dithiin as the predominant compounds, albeit in different ratios among genotypes. The bioactivity and the polar metab

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7

Garossian, Massoud. "HIGH YIELD SYNTHESIS OF α-PHOSPHONYL ORGANOSULFUR COMPOUNDS". Phosphorus, Sulfur, and Silicon and the Related Elements 88, № 1-4 (1994): 279–82. http://dx.doi.org/10.1080/10426509408036933.

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8

Singh, Yogendra P., and Ram A. Singh. "Insilico studies of organosulfur-functional active compounds in garlic." BioFactors 36, no. 4 (2010): 297–311. http://dx.doi.org/10.1002/biof.102.

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9

Matsuzawa, Tsubasa, Suguru Yoshida, and Takamitsu Hosoya. "Recent advances in reactions between arynes and organosulfur compounds." Tetrahedron Letters 59, no. 48 (2018): 4197–208. http://dx.doi.org/10.1016/j.tetlet.2018.10.031.

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10

Fukushima, Shoji, Nobuyasu Takada, Takaaki Hori, and Hideki Wanibuchi. "Cancer prevention by organosulfur compounds from garlic and onion." Journal of Cellular Biochemistry 67, S27 (1997): 100–105. http://dx.doi.org/10.1002/(sici)1097-4644(1997)27+<100::aid-jcb16>3.0.co;2-r.

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11

Yang, Qing, Qiuhui Hu, Osamu Yamatoc, Keun-Woo Lee, and Teruhiko Yoshihara. "Organosulfur Compounds from Garlic (Allium sativum) Oxidizing Canine Erythrocytes." Zeitschrift für Naturforschung C 58, no. 5-6 (2003): 408–12. http://dx.doi.org/10.1515/znc-2003-5-620.

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Abstract The sulfurous acid ester, trans-sulfurous acid allyl ester 3-allylsulfanyl-allyl ester 8, along with two known thiosulfinates was isolated from the aqueous ethanol extract of garlic (Allium sativum). The chemical structure of 8 was determined on the basis of spectroscopic data including high resolution mass and two-dimensional NMR techniques. All of these compounds induced methemoglobin formation in a canine erythrocyte suspension in vitro resulting in the oxidation of canine erythrocytes. This is the first report of sulfurous acid ester showing oxidant activity in canine erythrocytes

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12

Evans, David A., Margaret M. Faul, Lino Colombo, John J. Bisaha, Jon Clardy, and David Cherry. "Asymmetric synthesis of chiral organosulfur compounds using N-sulfinyloxazolidinones." Journal of the American Chemical Society 114, no. 15 (1992): 5977–85. http://dx.doi.org/10.1021/ja00041a011.

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13

Kim, Nak Doo, Sang Geon Kim, and Mi Kyong Kwak. "Enhanced expression of rat microsomal epoxide hydrolase gene by organosulfur compounds." Biochemical Pharmacology 47, no. 3 (1994): 541–47. http://dx.doi.org/10.1016/0006-2952(94)90186-4.

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14

Clark, Peter D., and Alex Primak. "The Preparation of Per-Deuterated Aromatic Hydrocarbons Using Organosulfur Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 74, no. 1-4 (1993): 413–14. http://dx.doi.org/10.1080/10426509308038141.

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15

Yu, Zhengkun, and John G. Verkade. "REDUCTIVE DESULFURIZATION OF ORGANOSULFUR COMPOUNDS WITH SODIUM IN LIQUID AMMONIA." Phosphorus, Sulfur, and Silicon and the Related Elements 133, no. 1 (1998): 79–82. http://dx.doi.org/10.1080/10426509808032455.

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16

Sundaravelu, Nallappan, Subramani Sangeetha, and Govindasamy Sekar. "Metal-catalyzed C–S bond formation using sulfur surrogates." Organic & Biomolecular Chemistry 19, no. 7 (2021): 1459–82. http://dx.doi.org/10.1039/d0ob02320e.

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This review presents the metal-catalyzed C–S bond-formation reaction to access organosulfur compounds using various sulfur surrogates with an extended discussion on the reaction mechanism, regioselectivity of product and pharmaceutical application.

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17

Schenk, Wolfdieter A., Jürgen Bezler, Nicolai Burzlaff, et al. "Stereo- and Enantioselective Reactions of Organosulfur Compounds Mediated by Transition Metal Complexes." Phosphorus, Sulfur, and Silicon and the Related Elements 95, no. 1-4 (1994): 367–70. http://dx.doi.org/10.1080/10426509408034239.

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18

Ganiyu, Saheed A. "Hierarchical Hybrid Supports and Synthesis Strategies for Hydrodesulfurization of Recalcitrance Organosulfur Compounds." Chemistry – An Asian Journal 16, no. 11 (2021): 1307–23. http://dx.doi.org/10.1002/asia.202100185.

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19

Mi Kyong Kwak, Sang Geon Kim, Ji Yeon Kwak, Raymond F. Novak, and Nak Doo Kim. "Inhibition of cytochrome P4502E1 expression by organosulfur compounds allylsulfide, allylmercaptan and allylmethylsulfide in rats." Biochemical Pharmacology 47, no. 3 (1994): 531–39. http://dx.doi.org/10.1016/0006-2952(94)90185-6.

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20

Clark, Peter D., and Alex Primak. "STUDIES ON THE DEUTERATION OF AROMATIC ORGANOSULFUR COMPOUNDS USING AQUEOUS TRANSITION METAL SPECIES." Phosphorus, Sulfur, and Silicon and the Related Elements 84, no. 1-4 (1993): 149–57. http://dx.doi.org/10.1080/10426509308034326.

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21

Akasaka, Takeshi, Takahiro Tsuchiya, Lai Feng, Yuta Takano, and Shigeru Nagase. "New Vistas in Fullerene Chemistry: Organosulfur Compounds Expand the Performance Of Carbon Nanomaterials." Phosphorus, Sulfur, and Silicon and the Related Elements 188, no. 4 (2013): 317–21. http://dx.doi.org/10.1080/10426507.2012.736109.

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22

Lamberth, Clemens, Harald Walter, Fiona Murphy Kessabi, et al. "The Significance of Organosulfur Compounds in Crop Protection: Current Examples from Fungicide Research." Phosphorus, Sulfur, and Silicon and the Related Elements 190, no. 8 (2015): 1225–35. http://dx.doi.org/10.1080/10426507.2014.984033.

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23

Arisawa, Mieko, Takuya Watanabe, and Masahiko Yamaguchi. "Direct transformation of organosulfur compounds to organophosphorus compounds: rhodium-catalyzed synthesis of 1-alkynylphosphine sulfides and acylphosphine sulfides." Tetrahedron Letters 52, no. 18 (2011): 2410–12. http://dx.doi.org/10.1016/j.tetlet.2011.02.112.

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24

El-khateeb*, Mohammad, Birgit Wolfsberger, and Wolfdieter A. Schenk*. "Sulfur(IV) compounds as ligands." Journal of Organometallic Chemistry 612, no. 1-2 (2000): 14–17. http://dx.doi.org/10.1016/s0022-328x(00)00346-6.

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25

Schenk, Wolfdieter A., Almuetassem Khadra, and Christian Burschka. "Sulphur(IV) compounds as ligands." Journal of Organometallic Chemistry 468, no. 1-2 (1994): 75–86. http://dx.doi.org/10.1016/0022-328x(94)80033-2.

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26

Alexis, Clive P., Juan M. Uribe, Jeffrey D. Beller, Gayane Godjoian, and Carlos G. Gutierrez. "POLYDENTATE SNXM(X = S,O,N) LIGANDS BY SELECTIVE REDUCTION OF ORGANOSULFUR HETEROCYCLES WITH TRIBUTYLTIN HYDRIDE." Phosphorus, Sulfur, and Silicon and the Related Elements 119, no. 1 (1996): 93–112. http://dx.doi.org/10.1080/10426509608043468.

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27

Doerge, Daniel R. "Oxygenation of organosulfur compounds by peroxidases: Evidence of an electron transfer mechanism for lactoperoxidase." Archives of Biochemistry and Biophysics 244, no. 2 (1986): 678–85. http://dx.doi.org/10.1016/0003-9861(86)90636-3.

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28

Hiroi, Kunio, Yoshio Suzuki, Ikuko Abe, Yutaka Hasegawa, and Kenji Suzuki. "ChemInform Abstract: Chiral Organosulfur Compounds. Part 7. Chiral Sulfoxide Ligands Bearing Nitrogen Atoms as Stereocontrollable Coordinating Elements in Palladium-Catalyzed Asymmetric Allylic Alkylations." ChemInform 30, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199916043.

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29

Ippoushi, Katsunari, Hidekazu Itou, Keiko Azuma, and Hisao Higashio. "Effect of naturally occurring organosulfur compounds on nitric oxide production in lipopolysaccharide-activated macrophages." Life Sciences 71, no. 4 (2002): 411–19. http://dx.doi.org/10.1016/s0024-3205(02)01685-5.

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30

Ayodele, Ezekiel T., Harry R. Hudson, Isaac A. O. Ojo, and Max Pianka. "ORGANOSULFUR COMPOUNDS AS POTENTIAL FUNGICIDES: THE PREPARATION AND PROPERTIES OF SOME SUBSTITUTED BENZYL 2-HYDROXYETHYL OLIGOSULFIDES." Phosphorus, Sulfur, and Silicon and the Related Elements 159, no. 1 (2000): 123–42. http://dx.doi.org/10.1080/10426500008043656.

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31

Cossu, Sergio, Ottorino De Lucchi, Elisabetta Piga, and Giovanni Valle. "HIGH-SYMMETRY CHIRAL ORGANOSULFUR COMPOUNDS: 6,7-DITHIO-DIBENZO[c,e][1,2]DITHIIN AND 5,6-DITHIO-DIBENZOTHIOPHENE." Phosphorus, Sulfur, and Silicon and the Related Elements 63, no. 1-2 (1991): 51–56. http://dx.doi.org/10.1080/10426509108029426.

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32

Ou, Chu-chyn, Shyh-ming Tsao, Ming-cheng Lin, and Mei-chin Yin. "Protective action on human LDL against oxidation and glycation by four organosulfur compounds derived from garlic." Lipids 38, no. 3 (2003): 219–24. http://dx.doi.org/10.1007/s11745-003-1054-4.

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33

Zamora-Rosete, M. Kenia, Diego Gorostieta, Raymundo Cea-Olivares, R. Alfredo Toscano, Simón Hernández-Ortega, and Verónica García-Montalvo. "Organotellurium(IV) Compounds Containing Symmetric Imidobis(Diphenylphosphinechalcogenide) Ligands." Phosphorus, Sulfur, and Silicon and the Related Elements 169, no. 1 (2001): 21–25. http://dx.doi.org/10.1080/10426500108546581.

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34

Farrar, T. C., Barry M. Trost, S. L. Tang, and S. E. Springer-Wilson. "Useful approach for determination of the structure of organosulfur compounds: sulfur-33 high-resolution FT-NMR." Journal of the American Chemical Society 107, no. 1 (1985): 262–64. http://dx.doi.org/10.1021/ja00287a054.

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35

Maeda, Yutaka, Junki Higo, Yuri Amagai, et al. "Helicity-Selective Photoreaction of Single-Walled Carbon Nanotubes with Organosulfur Compounds in the Presence of Oxygen." Journal of the American Chemical Society 135, no. 16 (2013): 6356–62. http://dx.doi.org/10.1021/ja402199n.

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36

Kothari, Damini, Woo-Do Lee, and Soo-Ki Kim. "Allium Flavonols: Health Benefits, Molecular Targets, and Bioavailability." Antioxidants 9, no. 9 (2020): 888. http://dx.doi.org/10.3390/antiox9090888.

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Allium species are revered worldwide as vegetables, condiments, and spices as well as the therapeutic agents in traditional medicine. The bioactive compounds in alliums mainly include organosulfur compounds, polyphenols, dietary fibers, and saponins. Flavonoids, particularly flavonols from alliums, have been demonstrated to have the antioxidant, anticancer, hypolipidemic, anti-diabetic, cardioprotective, neuroprotective, and antimicrobial activities. However, flavonols are mostly characterized from onions and have not been comprehensively reviewed across different species. This article therefo

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37

Jutzi, P., and J. Dahlhaus. "Organometallic Compounds with Bridged or (Dimethylaminoethyl)-Substituted Cyclopentadienyl Ligands." Phosphorus, Sulfur, and Silicon and the Related Elements 87, no. 1-4 (1994): 73–82. http://dx.doi.org/10.1080/10426509408037441.

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38

Jugé, Sylvain. "Designing P*-chirogenic Organophosphorus Compounds: from Ligands to Organocatalysts." Phosphorus, Sulfur, and Silicon and the Related Elements 190, no. 5-6 (2015): 600–611. http://dx.doi.org/10.1080/10426507.2014.999368.

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39

Chen, Chi, Daniel Pung, Vasco Leong, et al. "Induction of detoxifying enzymes by garlic organosulfur compounds through transcription factor Nrf2: effect of chemical structure and stress signals." Free Radical Biology and Medicine 37, no. 10 (2004): 1578–90. http://dx.doi.org/10.1016/j.freeradbiomed.2004.07.021.

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40

Block, Eric, Saleem Ahmad, James L. Catalfamo, Mahendra K. Jain, and Rafael Apitz-Castro. "The chemistry of alkyl thiosulfinate esters. 9. Antithrombotic organosulfur compounds from garlic: structural, mechanistic, and synthetic studies." Journal of the American Chemical Society 108, no. 22 (1986): 7045–55. http://dx.doi.org/10.1021/ja00282a033.

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41

Kao, James, Charles Eyermann, Everett Southwick, and Diane Leister. "A systematic approach to calculate molecular properties of organosulfur compounds containing the carbon-sulfur (Csp2-S) bond." Journal of the American Chemical Society 107, no. 19 (1985): 5323–32. http://dx.doi.org/10.1021/ja00305a001.

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42

Tokitoh, Norihiro, Masaki Takahashi, Tsuyoshi Matsumoto, Hiroyiki Suzuki, Yasusuke Matsuhashi, and Renji Okazaki. "SYNTHESIS AND REACTIONS OF NOVEL ORGANOSULFUR COMPOUNDS HAVING A HIGHLY STERICALLY BULKY GROUP, 2,4,6-TRIS[BIS(TRIMETHYLSILYL)METHYL]PHENYL." Phosphorus, Sulfur, and Silicon and the Related Elements 59, no. 1-4 (1991): 161–64. http://dx.doi.org/10.1080/10426509108045714.

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43

Pan, Jinmei, Hong Jun-Yan, Donna Li, et al. "Regulation of cytochrome P450 2B1/2 genes by diallyl sulfone, disulfiram, and other organosulfur compounds in primary cultures of rat hepatocytes." Biochemical Pharmacology 45, no. 11 (1993): 2323–29. http://dx.doi.org/10.1016/0006-2952(93)90206-c.

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44

Cady, Nathaniel C., Kurt A. McKean, Jason Behnke, et al. "Inhibition of Biofilm Formation, Quorum Sensing and Infection in Pseudomonas aeruginosa by Natural Products-Inspired Organosulfur Compounds." PLoS ONE 7, no. 6 (2012): e38492. http://dx.doi.org/10.1371/journal.pone.0038492.

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45

Hill, Michael S., Aaron R. Hutchison, Timothy S. Keizer, Sean Parkin, Michael A. VanAelstyn, and David A. Atwood. "Monomeric Group 13 compounds with bidentate (N,O) ligands." Journal of Organometallic Chemistry 628, no. 1 (2001): 71–75. http://dx.doi.org/10.1016/s0022-328x(01)00738-0.

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46

Piskunov, Alexandr V., Arina V. Lado, Ekaterina V. Ilyakina, et al. "New organobimetallic compounds containing catecholate and o-semiquinolate ligands." Journal of Organometallic Chemistry 693, no. 1 (2008): 128–34. http://dx.doi.org/10.1016/j.jorganchem.2007.10.029.

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47

Francioso, Antonio, Alessia Baseggio Conrado, Luciana Mosca, and Mario Fontana. "Chemistry and Biochemistry of Sulfur Natural Compounds: Key Intermediates of Metabolism and Redox Biology." Oxidative Medicine and Cellular Longevity 2020 (September 29, 2020): 1–27. http://dx.doi.org/10.1155/2020/8294158.

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Sulfur contributes significantly to nature chemical diversity and thanks to its particular features allows fundamental biological reactions that no other element allows. Sulfur natural compounds are utilized by all living beings and depending on the function are distributed in the different kingdoms. It is no coincidence that marine organisms are one of the most important sources of sulfur natural products since most of the inorganic sulfur is metabolized in ocean environments where this element is abundant. Terrestrial organisms such as plants and microorganisms are also able to incorporate s

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48

Nuzzo, Ralph G., Bernard R. Zegarski, and Lawrence H. Dubois. "Fundamental studies of the chemisorption of organosulfur compounds on gold(111). Implications for molecular self-assembly on gold surfaces." Journal of the American Chemical Society 109, no. 3 (1987): 733–40. http://dx.doi.org/10.1021/ja00237a017.

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49

Yatsimirskii, K. B., and L. V. Pisarzevsky. "Coordination Compounds of Alkali Metal Ions with Ligands Containing Phosphoryl Groups." Phosphorus, Sulfur, and Silicon and the Related Elements 49-50, no. 1-4 (1990): 417–20. http://dx.doi.org/10.1080/10426509008038992.

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50

Yang, Jie, Xin He, Zhen Ke, et al. "Two photoactive Ru (II) compounds based on tetrazole ligands for photodynamic therapy." Journal of Inorganic Biochemistry 210 (September 2020): 111127. http://dx.doi.org/10.1016/j.jinorgbio.2020.111127.

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