Novel 1,2,3-triazole compounds: Synthesis, In vitro xanthine oxidase inhibitory activity, and molecular docking studies
Tài liệu tham khảo
Zafar, 2018, Xanthine oxidase inhibitory and molecular docking studies on pyrimidones, Med. Chem., 14, 524, 10.2174/1573406413666171129224919
Masuoka, 2018, Characterization of the xanthine oxidase inhibitory activity of alk (en) yl phenols and related compounds, Phytochemistry, 155, 100, 10.1016/j.phytochem.2018.07.006
Mehta, 2014, Natural xanthine oxidase inhibitors for management of gout: a review, Research and reviews, J. Med. Health Sci., 3, 4
Bach, 2014, Uricosuric drugs: the once and future therapy for hyperuricemia?, Curr. Opin. Rheumatol., 26, 169, 10.1097/BOR.0000000000000035
Shi, 2019, Alkaloids isolated from Tabernaemontana bufalina display xanthine oxidase inhibitory activity, Phytochemistry, 166, 112060, 10.1016/j.phytochem.2019.112060
Pascart, 2018, Colchicine in gout: an update, Curr. Pharmaceut. Des., 24, 684, 10.2174/1381612824999180115103951
Greig, 2016, Loxoprofen: a review in pain and inflammation, Clin. Drug Invest., 36, 771, 10.1007/s40261-016-0440-9
Baldwin, 1975, 4-Trifluoromethylimidazoles and 5-(4-pyridyl)-1, 2, 4-triazoles, new classes of xanthine oxidase inhibitors, J. Med. Chem., 18, 895, 10.1021/jm00243a007
Krishnamurthy, 2015, Febuxostat ameliorates doxorubicin-induced cardiotoxicity in rats, Chem. Biol. Interact., 237, 96, 10.1016/j.cbi.2015.05.013
Phatak, 2019, Synthesis, antitubercular evaluation and molecular docking studies of phthalimide bearing 1,2,3-triazoles, Synth. Commun., 49, 2017, 10.1080/00397911.2019.1614630
Rajasekar, 2019, A general proline catalyzed synthesis of 4, 5-disubstituted N-Sulfonyl-1, 2, 3-triazoles from 1, 3-dicarbonyl compounds and sulfonyl azide, Chem.–An Asian J., 10.1002/asia.201901015
Kushwaha, 2014, Design and synthesis of novel 2H-chromen-2-one derivatives bearing 1, 2, 3-triazole moiety as lead antimicrobials, Bioorg. Med. Chem. Lett, 24, 1795, 10.1016/j.bmcl.2014.02.027
Wang, 2016, Synthesis and biological evaluation of novel 2, 4, 5-triarylimidazole–1, 2, 3-triazole derivatives via click chemistry as α-glucosidase inhibitors, Bioorg. Med. Chem. Lett, 26, 5719, 10.1016/j.bmcl.2016.10.057
Gong, 2017, Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of novel benzothiazole-triazole derivatives, Molecules, 22, 1555, 10.3390/molecules22091555
Li, 2012, Facile synthesis of 1, 2, 3-triazole analogs of SGLT2 inhibitors by ‘click chemistry, Bioorg. Med. Chem. Lett, 22, 642, 10.1016/j.bmcl.2011.10.062
Röhrig, 2012, Rational design of 4-aryl-1, 2, 3-triazoles for indoleamine 2, 3-dioxygenase 1 inhibition, J. Med. Chem., 55, 5270, 10.1021/jm300260v
González-Olvera, 2013, Multicomponent click synthesis of new 1, 2, 3-triazole derivatives of pyrimidine nucleobases: promising acidic corrosion inhibitors for steel, Molecules, 18, 15064, 10.3390/molecules181215064
Xavier, 2014, Triazole-containing carbohydrate mimetics: synthesis and biological applications, Targets Heterocyc.Syst.: Chem. Prop., 18, 214
Vats, 2018, Synthesis of novel 4-functionalized 1, 5-diaryl-1, 2, 3-triazoles containing benzenesulfonamide moiety as carbonic anhydrase I, II, IV and IX inhibitors, Eur. J. Med. Chem., 150, 678, 10.1016/j.ejmech.2018.03.030
Banachowicz, 2019, Gram-scale carbasugar synthesis via intramolecular seleno-Michael/aldol reaction, RSC Adv., 9, 12928, 10.1039/C9RA02002K
Narayana, 2018, Design and synthesis of N–acetylglucosamine derived 5a-carbasugar analogues as glycosidase inhibitors, Tetrahedron, 74, 1957, 10.1016/j.tet.2018.02.063
Witte, 2010, Ultrasensitive in situ visualization of active glucocerebrosidase molecules, Nat. Chem. Biol., 6, 907, 10.1038/nchembio.466
Brazdova, 2009, Novel easily accessible glucosidase inhibitors: 4-hydroxy-5-alkoxy-1, 2-cyclohexanedicarboxylic acids, Carbohydr. Res., 344, 311, 10.1016/j.carres.2008.11.009
Patel, 2019, A practical green visit to the functionalized [1, 2, 4] triazolo [5, 1-b] quinazolin-8 (4H) one scaffolds using the group-assisted purification (GAP) chemistry and their pharmacological testing, Chemistry, 4, 1031
Payra, 2018, On water Cu@ g-C3N4 catalyzed synthesis of NH-1, 2, 3-triazoles via [2+3] cycloadditions of nitroolefins/alkynes and sodium azide, ChemCatChem, 10, 5468, 10.1002/cctc.201801524
Worrell, 2013, Direct evidence of a dinuclear copper intermediate in Cu (I)-catalyzed azide-alkyne cycloadditions, Science, 340, 457, 10.1126/science.1229506
Patel, 2018, Synthesis, characterizations and microbial studies of novel mannich products using multicomponent reactions, Curr. Bioact. Compd., 14, 278, 10.2174/1573407213666170424164716
Patel, 2015, Synthesis of new mannich products bearing quinoline nucleous using reusable ionic liquid and antitubercular evaluation, Green Sustain. Chem., 5, 137, 10.4236/gsc.2015.54017
Sweeney, 2001, Xanthine oxidase inhibitory activity of selected Australian native plants, J. Ethnopharmacol., 75, 273, 10.1016/S0378-8741(01)00176-3
Nile, 2013, In vitro evaluation of selected benzimidazole derivatives as an antioxidant and xanthine oxidase inhibitors, Chem. Biol. Drug Des., 82, 290, 10.1111/cbdd.12141
Hassan, 2017, Pharmacoinformatics exploration of polyphenol oxidases leading to novel inhibitors by virtual screening and molecular dynamic simulation study, Comput. Biol. Chem., 68, 131, 10.1016/j.compbiolchem.2017.02.012
Hassan, 2018, Exploration of novel human tyrosinase inhibitors by molecular modeling, docking and simulation studies, Interdiscipl. Sci. Comput. Life Sci., 10, 68, 10.1007/s12539-016-0171-x
Patel, 2019, Synthesis, molecular docking and biological evaluation of mannich products based on thiophene nucleus using ionic liquid, Lett. Drug Des. Discov., 16, 119, 10.2174/1570180815666180502123743
Patel, 2017, Facile synthesis and biological evaluation of New Mannich products as potential antibacterial, antifungal and antituberculosis agents: molecular docking study, Curr. Bioact. Compd., 13, 47, 10.2174/1573407212666160517145130
Pettersen, 2004, UCSF Chimera—a visualization system for exploratory research and analysis, J. Comput. Chem., 25, 1605, 10.1002/jcc.20084
Berman, 2000, The protein data Bank, Nucleic Acids Res., 28, 235, 10.1093/nar/28.1.235
Hanwell, 2012, Avogadro: an advanced semantic chemical editor, visualization, and analysis platform, J. Cheminf., 4, 17, 10.1186/1758-2946-4-17
Trott, 2010, Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading, J. Comput. Chem., 31, 455
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