Статті в журналах з теми "Saligenin"
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Bakker, Daniël J., Arghya Dey, Daniel P. Tabor, Qin Ong, Jérôme Mahé, Marie-Pierre Gaigeot, Edwin L. Sibert, and Anouk M. Rijs. "Fingerprints of inter- and intramolecular hydrogen bonding in saligenin–water clusters revealed by mid- and far-infrared spectroscopy." Physical Chemistry Chemical Physics 19, no. 31 (2017): 20343–56. http://dx.doi.org/10.1039/c7cp01951c.
Повний текст джерелаSaragi, Rizalina Tama, Marcos Juanes, José Luis Abad, Alberto Lesarri, Ruth Pinacho, and José Emiliano Rubio. "Rotational spectroscopy of organophosphorous chemical agents: cresyl and phenyl saligenin phosphates." Physical Chemistry Chemical Physics 21, no. 30 (2019): 16418–22. http://dx.doi.org/10.1039/c9cp03093j.
Повний текст джерелаGlynn, P., D. J. Read, R. Guo, S. Wylie, and M. K. Johnson. "Synthesis and characterization of a biotinylated organophosphorus ester for detection and affinity purification of a brain serine esterase: neuropathy target esterase." Biochemical Journal 301, no. 2 (July 15, 1994): 551–56. http://dx.doi.org/10.1042/bj3010551.
Повний текст джерелаSingh, Vishwakarma, Punitha Vedantham, and Pramod K. Sahu. "A novel stereoselective total synthesis of (±)-hirsutene from saligenin." Tetrahedron Letters 43, no. 3 (January 2002): 519–22. http://dx.doi.org/10.1016/s0040-4039(01)02183-9.
Повний текст джерелаLushchekina, S. V., V. S. Polomskikh, S. D. Varfolomeev, and P. Masson. "Molecular modeling of butyrylcholinesterase inhibition by cresyl saligenin phosphate." Russian Chemical Bulletin 62, no. 11 (November 2013): 2527–37. http://dx.doi.org/10.1007/s11172-013-0366-9.
Повний текст джерелаShiotsuki, Takahiro, Takeshi Kakimoto, and Morifusa Eto. "Irreversible inactivation of glutathione transferases by saligenin cyclic phosphates." Pesticide Biochemistry and Physiology 42, no. 2 (February 1992): 119–27. http://dx.doi.org/10.1016/0048-3575(92)90059-9.
Повний текст джерелаSHIOTSUKI, Takahiro. "Mode of Action of Saligenin Cyclic Phosphates on Organophosphate-Resistant Houseflies." Journal of Pesticide Science 16, no. 3 (1991): 523–31. http://dx.doi.org/10.1584/jpestics.16.523.
Повний текст джерелаLidsky, T. I., C. Manetto, and M. Ehrich. "Nerve conduction studies in chickens given phenyl saligenin phosphate and corticosterone." Journal of Toxicology and Environmental Health 29, no. 1 (January 1990): 65–75. http://dx.doi.org/10.1080/15287399009531372.
Повний текст джерелаTorgul, M., M. SÜnkÜr, F. B. Kaynak, H. HosgOren, and S. Ozbey. "Saligenin derivative borocryptands: synthesis and structural analysis of new type lithium borocryptate." Journal of Chemical Research (Miniprint) 2003, no. 10 (October 1, 2003): 605. http://dx.doi.org/10.3184/030823503322655670.
Повний текст джерелаTogrul, M., M. SÜnkÜr, F. B. Kaynak, H. HosgOren, and S. Ozbey. "Saligenin derivative borocryptands: synthesis and structural analysis of new type lithium borocryptate." Journal of Chemical Research 2003, no. 10 (October 1, 2003): 605. http://dx.doi.org/10.3184/030823403322655770.
Повний текст джерелаSHIOTSUKI, Takahiro, Akihiro KOISO, and Morifusa ETO. "Glutathione Conjugation as a Mechanism for Glutathione Transferase Inhibition by Saligenin Cyclic Phosphates." Journal of Pesticide Science 14, no. 3 (1989): 337–44. http://dx.doi.org/10.1584/jpestics.14.337.
Повний текст джерелаXu, Lin-Lin, Meng-Ling Liu, Jing-Lei Wang, Mei Yu, and Jia-Xiang Chen. "Saligenin cyclic-o-tolyl phosphate (SCOTP) induces autophagy of rat spermatogonial stem cells." Reproductive Toxicology 60 (April 2016): 62–68. http://dx.doi.org/10.1016/j.reprotox.2016.01.004.
Повний текст джерелаJortner, B. S., and M. Enrich. "PATHOLOGICAL EFFECTS OF PHENYL SALIGENIN PHOSPHATE, A POTENT NEUROTOXIC CONGENER OF TRIORTHOTOLYL PHOSPHATE." Journal of Neuropathology and Experimental Neurology 45, no. 3 (May 1986): 359. http://dx.doi.org/10.1097/00005072-198605000-00134.
Повний текст джерелаFlaskos, John, Magdalini Sachana, Michèle Pen, Wayne C. Harris, and Alan J. Hargreaves. "Effects of phenyl saligenin phosphate on phosphorylation of pig brain tubulin in vitro." Environmental Toxicology and Pharmacology 22, no. 1 (July 2006): 70–74. http://dx.doi.org/10.1016/j.etap.2005.12.006.
Повний текст джерелаSaracila, Mihaela, Tatiana Dumitra Panaite, Camelia Puia Papuc, and Rodica Diana Criste. "Heat Stress in Broiler Chickens and the Effect of Dietary Polyphenols, with Special Reference to Willow (Salix spp.) Bark Supplements—A Review." Antioxidants 10, no. 5 (April 27, 2021): 686. http://dx.doi.org/10.3390/antiox10050686.
Повний текст джерелаBosak, Anita, Anamarija Knežević, Ivana Gazić Smilović, Goran Šinko та Zrinka Kovarik. "Resorcinol-, catechol- and saligenin-based bronchodilating β2-agonists as inhibitors of human cholinesterase activity". Journal of Enzyme Inhibition and Medicinal Chemistry 32, № 1 (1 січня 2017): 789–97. http://dx.doi.org/10.1080/14756366.2017.1326109.
Повний текст джерелаKnežević, Anamarija, Jurica Novak, Anita Bosak та Marijana Vinković. "Structural isomers of saligenin-based β2-agonists: synthesis and insight into the reaction mechanism". Organic & Biomolecular Chemistry 18, № 47 (2020): 9675–88. http://dx.doi.org/10.1039/d0ob02095h.
Повний текст джерелаBurka, Leo T., and Robert E. Chapin. "Toxicokinetics of [14C]-saligenin cyclic-o-tolyl phosphate in anesthetized male F-344 rats." Reproductive Toxicology 7, no. 1 (January 1993): 81–86. http://dx.doi.org/10.1016/0890-6238(93)90013-w.
Повний текст джерелаProcopiou, Panayiotis A., Victoria J. Barrett, Alison J. Ford, Brian E. Looker, Gillian E. Lunniss, Deborah Needham, Claire E. Smith та Graham Somers. "The discovery of long-acting saligenin β2 adrenergic receptor agonists incorporating a urea group". Bioorganic & Medicinal Chemistry 19, № 20 (жовтень 2011): 6026–32. http://dx.doi.org/10.1016/j.bmc.2011.08.043.
Повний текст джерелаKuran, Witold, and Ewa Mazanek. "Synthesis of novel monomeric zinc—oxygen compounds containing diethylzinc and pyrocatechol or saligenin moieties." Journal of Organometallic Chemistry 384, no. 1-2 (February 1990): 13–17. http://dx.doi.org/10.1016/0022-328x(90)87048-i.
Повний текст джерелаKakimoto, Takeshi, Takahiro Shiotsuki, and Morifusa Eto. "Reaction of Saligenin Cyclic Phosphorus Esters with Some Amino Acids and Purine and Pyrimidine Bases." Journal of the Faculty of Agriculture, Kyushu University 37, no. 3/4 (March 1993): 371–77. http://dx.doi.org/10.5109/24030.
Повний текст джерелаMentzschel, Anke, Gabi Schmuck, Wolfgang Dekant, and Dietrich Henschler. "Genotoxicity of neurotoxic triaryl phosphates: Identification of DNA adducts of the ultimate metabolites, saligenin phosphates." Chemical Research in Toxicology 6, no. 3 (May 1993): 294–301. http://dx.doi.org/10.1021/tx00033a007.
Повний текст джерелаProcopiou, Panayiotis A., Victoria J. Barrett, Nicola J. Bevan, Peter R. Butchers, Richard Conroy, Amanda Emmons, Alison J. Ford та ін. "The discovery of long-acting saligenin β2 adrenergic receptor agonists incorporating hydantoin or uracil rings". Bioorganic & Medicinal Chemistry 19, № 14 (липень 2011): 4192–201. http://dx.doi.org/10.1016/j.bmc.2011.05.064.
Повний текст джерелаBursian, S. J., E. J. Lehning, L. Correll та M. Ehrich. "Effect of β‐naphthoflavone ono‐tolyl saligenin phosphate‐induced delayed neuropathy in two lines of chickens". Journal of Toxicology and Environmental Health 28, № 4 (грудень 1989): 461–71. http://dx.doi.org/10.1080/15287398909531364.
Повний текст джерелаShiotsuki, Takahiro, Akihiro Koiso, and Morifusa Eto. "Inhibition of glutathione transferase by S-benzyl glutathione analogous to the conjugate of saligenin cyclic phosphate." Pesticide Biochemistry and Physiology 37, no. 2 (June 1990): 121–29. http://dx.doi.org/10.1016/0048-3575(90)90117-k.
Повний текст джерелаRishina, Laura A., Svetlana S. Lalayan, Svetlana C. Gagieva, Vladislav A. Tuskaev, Evgeniya O. Perepelitsyna, and Yury V. Kissin. "Polymers of propylene and higher 1-alkenes produced with post-metallocene complexes containing a saligenin-type ligand." Polymer 54, no. 24 (November 2013): 6526–35. http://dx.doi.org/10.1016/j.polymer.2013.09.052.
Повний текст джерелаFelemban, Shatha G., A. Christopher Garner, Fathi A. Smida, David J. Boocock, Alan J. Hargreaves, and John M. Dickenson. "Phenyl Saligenin Phosphate Induced Caspase-3 and c-Jun N-Terminal Kinase Activation in Cardiomyocyte-Like Cells." Chemical Research in Toxicology 28, no. 11 (October 23, 2015): 2179–91. http://dx.doi.org/10.1021/acs.chemrestox.5b00338.
Повний текст джерелаPruett, Stephen B., and Janice E. Chambers. "Effects of paraoxon, p-nitrophenol, phenyl saligenin cyclic phosphate, and phenol on the rat interleukin 2 system." Toxicology Letters 40, no. 1 (January 1988): 11–20. http://dx.doi.org/10.1016/0378-4274(88)90178-6.
Повний текст джерелаEhrich, Marion, Linda Shell, Michael Rozum, and B. S. Jortner. "Short-term Clinical and Neuropathologic Effects of Cholinesterase Inhibitors in Rats." Journal of the American College of Toxicology 12, no. 1 (January 1993): 55–68. http://dx.doi.org/10.3109/10915819309140622.
Повний текст джерелаDucho, Christian, Jan Balzarini, Lieve Naesens, Erik De Clercq, and Chris Meier. "Aryl-Substituted and Benzo-Annulated CycloSal-Derivatives of 2′,3′-Dideoxy-2′,3′-Didehydrothymidine Monophosphate — Correlation of Structure, Hydrolysis Properties and Anti-HIV Activity." Antiviral Chemistry and Chemotherapy 13, no. 2 (April 2002): 129–41. http://dx.doi.org/10.1177/095632020201300206.
Повний текст джерелаMassicotte, Christiane, David S. Barber, Bernard S. Jortner, and Marion Ehrich. "Nerve Conduction and ATP Concentrations in Sciatic-Tibial and Medial Plantar Nerves of Hens Given Phenyl Saligenin Phosphate." NeuroToxicology 22, no. 1 (February 2001): 91–98. http://dx.doi.org/10.1016/s0161-813x(00)00004-8.
Повний текст джерелаKumar, Sumit, Santosh K. Singh, Camilla Calabrese, Assimo Maris, Sonia Melandri, and Aloke Das. "Structure of saligenin: microwave, UV and IR spectroscopy studies in a supersonic jet combined with quantum chemistry calculations." Physical Chemistry Chemical Physics 16, no. 32 (July 10, 2014): 17163. http://dx.doi.org/10.1039/c4cp01693a.
Повний текст джерелаRishina, Laura, Svetlana Lalayan, Svetlana Gagieva, Vladislav Тuskaev, Alexander Shchegolikhin, Dimitri Shashkin та Yury Kissin. "Titanium Complex Containing a Saligenin Ligand - New Universal Post-Metallocene Polymerization Catalyst: Copolymerization of Ethylene with Higher α-Olefins". Journal of Research Updates in Polymer Science 3, № 4 (5 січня 2015): 216–26. http://dx.doi.org/10.6000/1929-5995.2014.03.04.3.
Повний текст джерелаMcCain, W. C., J. Wilcke, J. C. Lee, and M. Ehrich. "Effect of cyclic phenyl saligenin phosphate and paraoxon treatment on vascular response to adrenergic and cholinergic agents in hens." Journal of Toxicology and Environmental Health 44, no. 2 (February 1995): 167–87. http://dx.doi.org/10.1080/15287399509531953.
Повний текст джерелаHarp, Paul, Duke Tanaka, and Carey N. Pope. "Potentiation of Organophosphorus-Induced Delayed Neurotoxicity Following Phenyl Saligenin Phosphate Exposures in 2-, 5-, and 8-Week-Old Chickens." Toxicological Sciences 37, no. 1 (1997): 64–70. http://dx.doi.org/10.1093/toxsci/37.1.64.
Повний текст джерелаHarris, W., D. Muñoz, P. L. R. Bonner, and A. J. Hargreaves. "Effects of phenyl saligenin phosphate on cell viability and transglutaminase activity in N2a neuroblastoma and HepG2 hepatoma cell lines." Toxicology in Vitro 23, no. 8 (December 2009): 1559–63. http://dx.doi.org/10.1016/j.tiv.2009.08.029.
Повний текст джерелаLiyasova, Mariya S., Lawrence M. Schopfer, and Oksana Lockridge. "Cresyl Saligenin Phosphate, an Organophosphorus Toxicant, Makes Covalent Adducts with Histidine, Lysine, and Tyrosine Residues of Human Serum Albumin." Chemical Research in Toxicology 25, no. 8 (July 26, 2012): 1752–61. http://dx.doi.org/10.1021/tx300215g.
Повний текст джерелаHarp, P. "Potentiation of Organophosphorus-Induced Delayed Neurotoxicity Following Phenyl Saligenin Phosphate Exposures in 2-, 5-, and 8-Week-Old Chickens." Fundamental and Applied Toxicology 37, no. 1 (May 1997): 64–70. http://dx.doi.org/10.1006/faat.1997.2301.
Повний текст джерелаMccain, W. C., J. C. Lee, J. R. Wilcke, and M. Ehrich. "The Effect of Phenyl Saligenin Cyclic Phosphate Induced Delayed Neuropathy on Selected Hemodynamic and Hematologic Parameters in the Hen." Pesticide Biochemistry and Physiology 45, no. 3 (March 1993): 220–27. http://dx.doi.org/10.1006/pest.1993.1024.
Повний текст джерелаHausherr, Vanessa, Nicole Schöbel, Julia Liebing, and Christoph van Thriel. "Assessment of neurotoxic effects of tri-cresyl phosphates (TCPs) and cresyl saligenin phosphate (CBDP) using a combination of in vitro techniques." NeuroToxicology 59 (March 2017): 210–21. http://dx.doi.org/10.1016/j.neuro.2016.06.005.
Повний текст джерелаLiyasova, Mariya S., Lawrence M. Schopfer, and Oksana Lockridge. "Cresyl saligenin phosphate makes multiple adducts on free histidine, but does not form an adduct on histidine 438 of human butyrylcholinesterase." Chemico-Biological Interactions 203, no. 1 (March 2013): 103–7. http://dx.doi.org/10.1016/j.cbi.2012.07.006.
Повний текст джерелаFox, Jonathan H., Bernard S. Jortner, David Barber, and Marion F. Ehrich. "Altered expression of transcripts for ?-tubulin and an unidentified gene in the spinal cord of phenyl saligenin phosphate treated hens (Gallus gallus)." Journal of Biochemical and Molecular Toxicology 17, no. 5 (2003): 263–71. http://dx.doi.org/10.1002/jbt.10088.
Повний текст джерелаMasson, Patrick, Sofya Lushchekina, Lawrence M. Schopfer, and Oksana Lockridge. "Effects of viscosity and osmotic stress on the reaction of human butyrylcholinesterase with cresyl saligenin phosphate, a toxicant related to aerotoxic syndrome: kinetic and molecular dynamics studies." Biochemical Journal 454, no. 3 (August 29, 2013): 387–99. http://dx.doi.org/10.1042/bj20130389.
Повний текст джерелаAlmami, Ibtesam S., Maha A. Aldubayan, Shatha G. Felemban, Najiah Alyamani, Richard Howden, Alexander J. Robinson, Tom D. Z. Pearson, et al. "Neurite outgrowth inhibitory levels of organophosphates induce tissue transglutaminase activity in differentiating N2a cells: evidence for covalent adduct formation." Archives of Toxicology 94, no. 11 (August 4, 2020): 3861–75. http://dx.doi.org/10.1007/s00204-020-02852-w.
Повний текст джерелаCarlson, Kent, and Marion Ehrich. "Organophosphorus Compound–Induced Delayed Neurotoxicity in White Leghorn Hens Assessed by Fluoro-Jade." International Journal of Toxicology 23, no. 4 (July 2004): 259–66. http://dx.doi.org/10.1080/10915810490504968.
Повний текст джерелаFelemban, Shatha G., Falguni S. Vyas, Lyndsey Durose, Alan J. Hargreaves, and John M. Dickenson. "Phenyl Saligenin Phosphate Disrupts Cell Morphology and the Actin Cytoskeleton in Differentiating H9c2 Cardiomyoblasts and Human-Induced Pluripotent Stem-Cell-Derived Cardiomyocyte Progenitor Cells." Chemical Research in Toxicology 33, no. 9 (August 6, 2020): 2310–23. http://dx.doi.org/10.1021/acs.chemrestox.0c00100.
Повний текст джерелаMcCain, Wilfred C., Diane M. Flaherty, Linda Correll, Bernard Jortner, and Marion Ehrich. "CATECHOLAMINE CONCENTRATIONS AND CONTRACTILE RESPONSES OF ISOLATED VESSELS FROM HENS TREATED WITH CYCLIC PHENYL SALIGENIN PHOSPHATE OR PARAOXON IN THE PRESENCE OR ABSENCE OF VERAPAMIL." Journal of Toxicology and Environmental Health 48, no. 4 (July 1996): 397–411. http://dx.doi.org/10.1080/009841096161276.
Повний текст джерелаKart, Asim, and Ali Bilgili. "Effects of organophosphate phenyl saligenin phosphate and polyether carboxylic ionophore lasalocid on motor nerve conduction velocity, neuropathy target esterase enzyme activity, and clinical ataxia in chickens." Toxicology Mechanisms and Methods 19, no. 5 (June 2009): 351–55. http://dx.doi.org/10.1080/15376510903030403.
Повний текст джерелаCarletti, Eugénie, Lawrence M. Schopfer, Jacques-Philippe Colletier, Marie-Thérèse Froment, Florian Nachon, Martin Weik, Oksana Lockridge, and Patrick Masson. "Reaction of Cresyl Saligenin Phosphate, the Organophosphorus Agent Implicated in Aerotoxic Syndrome, with Human Cholinesterases: Mechanistic Studies Employing Kinetics, Mass Spectrometry, and X-ray Structure Analysis." Chemical Research in Toxicology 24, no. 6 (June 20, 2011): 797–808. http://dx.doi.org/10.1021/tx100447k.
Повний текст джерелаDuysen, Ellen G., John R. Cashman, Lawrence M. Schopfer, Florian Nachon, Patrick Masson, and Oksana Lockridge. "Differential sensitivity of plasma carboxylesterase-null mice to parathion, chlorpyrifos and chlorpyrifos oxon, but not to diazinon, dichlorvos, diisopropylfluorophosphate, cresyl saligenin phosphate, cyclosarin thiocholine, tabun thiocholine, and carbofuran." Chemico-Biological Interactions 195, no. 3 (February 2012): 189–98. http://dx.doi.org/10.1016/j.cbi.2011.12.006.
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