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For: Xu Z. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). Eur J Med Chem 2020;206:112686. [PMID: 32795773 DOI: 10.1016/j.ejmech.2020.112686] [Cited by in Crossref: 37] [Cited by in F6Publishing: 39] [Article Influence: 12.3] [Reference Citation Analysis]
Number Citing Articles
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6 Bianco MDCAD, Inacio Leite D, Silva Castelo Branco F, Boechat N, Uliassi E, Bolognesi ML, Bastos MM. The Use of Zidovudine Pharmacophore in Multi-Target-Directed Ligands for AIDS Therapy. Molecules 2022;27. [PMID: 36500608 DOI: 10.3390/molecules27238502] [Reference Citation Analysis]
7 Deng C, Yan H, Wang J, Liu K, Liu B, Shi Y. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against ESKAPE pathogens. European Journal of Medicinal Chemistry 2022;244:114888. [DOI: 10.1016/j.ejmech.2022.114888] [Reference Citation Analysis]
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9 Lengerli D, Ibis K, Nural Y, Banoglu E. The 1,2,3-triazole 'all-in-one' ring system in drug discovery: a good bioisostere, a good pharmacophore, a good linker, and a versatile synthetic tool. Expert Opin Drug Discov 2022;17:1209-36. [PMID: 36164263 DOI: 10.1080/17460441.2022.2129613] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Alqarni MH, Foudah AI, Alam A, Salkini MA, Muharram MM, Labrou NE, Rawat P. Coumarin-Encapsulated Solid Lipid Nanoparticles as an Effective Therapy against Methicillin-Resistant Staphylococcus aureus. Bioengineering 2022;9:484. [DOI: 10.3390/bioengineering9100484] [Reference Citation Analysis]
11 Gulledge ZZ, Duda DP, Dixon DA, Carrick JD. Microwave-Assisted, Metal- and Azide-Free Synthesis of Functionalized Heteroaryl-1,2,3-triazoles via Oxidative Cyclization of N-Tosylhydrazones and Anilines. J Org Chem 2022. [PMID: 36126149 DOI: 10.1021/acs.joc.2c01042] [Reference Citation Analysis]
12 Ben Hammouda M, Ahmad I, Hamdi A, Dbeibia A, Patel H, Bouali N, Sabri Hamadou W, Hosni K, Ghannay S, Alminderej F, Noumi E, Snoussi M, Aouadi K, Kadri A. Design, synthesis, biological evaluation and in silico studies of novel 1,2,3-triazole linked benzoxazine-2,4-dione conjugates as potent antimicrobial, antioxidant and anti-inflammatory agents. Arabian Journal of Chemistry 2022. [DOI: 10.1016/j.arabjc.2022.104226] [Reference Citation Analysis]
13 N MK, Nukala SK, Thirukovela NS, Sreerama R, E RS, Kamarajugadda P, Narsimha S. Ramachary-Bressy-Wang [3+2]cycloaddition reaction: Synthesis of fully decorated 1,2,3-triazoles as potent anticancer and EGFR inhibitors. Journal of Molecular Structure 2022;1262:132975. [DOI: 10.1016/j.molstruc.2022.132975] [Reference Citation Analysis]
14 Du T, Cao J, Xiao Z, Liu J, Wei L, Li C, Jiao J, Song Z, Liu J, Du X, Wang S. Van-mediated self-aggregating photothermal agents combined with multifunctional magnetic nickel oxide nanoparticles for precise elimination of bacterial infections. J Nanobiotechnology 2022;20:325. [PMID: 35836225 DOI: 10.1186/s12951-022-01535-1] [Reference Citation Analysis]
15 Wang X, Wang R, Zhang Z, Zhang G, Jin Z, Shen R, Du D, Tang Y. Semisynthetic pleuromutilin antimicrobials with therapeutic potential against methicillin-resistant Staphylococcus aureus by targeting 50S ribosomal subunit. European Journal of Medicinal Chemistry 2022;237:114341. [DOI: 10.1016/j.ejmech.2022.114341] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Ewies EF, Sabry E, Bekheit MS, Fouad MA, Vullo D, Supuran CT. Click chemistry-based synthesis of new benzenesulfonamide derivatives bearing triazole ring as selective carbonic anhydrase II inhibitors. Drug Dev Res 2022. [PMID: 35706360 DOI: 10.1002/ddr.21957] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Haq FU, Imran M, Saleem S, Aftab U, Ghazal A. Investigation of Morchella esculenta and Morchella conica for their antibacterial potential against methicillin-susceptible Staphylococcus aureus, methicillin-resistant Staphylococcus aureus and Streptococcus pyogenes. Arch Microbiol 2022;204:391. [PMID: 35699800 DOI: 10.1007/s00203-022-03003-8] [Reference Citation Analysis]
18 Tedder ML, Dzeagu FO, Mason MM, Dixon DA, Carrick JD. Microwave-assisted C–H oxidation of methylpyridylheteroarenes via a Kornblum-Type reaction. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132805] [Reference Citation Analysis]
19 Begam R, Shajahan A, Shefin B, Murugan V. Synthesis of novel naphthalimide tethered 1,2,3-triazoles: In vitro biological evaluation and docking study of anti-inflammatory inhibitors. Journal of Molecular Structure 2022;1254:132364. [DOI: 10.1016/j.molstruc.2022.132364] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
20 Zha L, Xie Y, Wu C, Lei M, Lu X, Tang W, Zhang J. Novel benzothiazole‒urea hybrids: Design, synthesis and biological activity as potent anti-bacterial agents against MRSA. Eur J Med Chem 2022;236:114333. [PMID: 35397402 DOI: 10.1016/j.ejmech.2022.114333] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Siddiqui MM, Nagargoje AA, Raza AK, Pisal PM, Shingate BB. [Et 3 NH][HSO 4 ] catalyzed solvent‐free synthesis of new 1,2,3‐triazolidene‐indolinone derivatives. Journal of Heterocyclic Chem. [DOI: 10.1002/jhet.4429] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Kumar AK, Sunitha V, Ramesh G, Jeshma K. Development of New Molecular Entities as Potent Antifungal Agents: Synthesis of Substituted 1,2,3-Triazoles. Russ J Gen Chem 2021;91:2546-53. [DOI: 10.1134/s1070363221120264] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Palchykov V, Manko N, Finiuk N, Stoika R, Obushak M, Pokhodylo N. Antimicrobial action of arylsulfonamides bearing (aza)norbornane and related motifs: evaluation of new promising anti-MRSA agents. Med Chem Res 2022;31:284-92. [DOI: 10.1007/s00044-021-02827-1] [Reference Citation Analysis]
24 Pingaew R, Choomuenwai V, Leechaisit R, Prachayasittikul V, Prachayasittikul S, Prachayasittikul V. 1,2,3-Triazole Scaffold in Recent Medicinal Applications: Synthesis and Anticancer Potentials. HETEROCYCLES 2022;105:147. [DOI: 10.3987/rev-22-sr(r)4] [Reference Citation Analysis]
25 Poonia N, Lal K, Kumar A, Kumar A, Sahu S, Baidya ATK, Kumar R. Urea-thiazole/benzothiazole hybrids with a triazole linker: synthesis, antimicrobial potential, pharmacokinetic profile and in silico mechanistic studies. Mol Divers 2021. [PMID: 34671895 DOI: 10.1007/s11030-021-10336-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
26 Danne AB, Deshpande MV, Sangshetti JN, Khedkar VM, Shingate BB. New 1,2,3-Triazole-Appended Bis-pyrazoles: Synthesis, Bioevaluation, and Molecular Docking. ACS Omega 2021;6:24879-90. [PMID: 34604669 DOI: 10.1021/acsomega.1c03734] [Reference Citation Analysis]
27 Mohamed KS, Elbialy EE, Fadda AA. Application of N-(Aryl)-2-oxo-2-(arylamino)acetohydrazonoyl Cyanide in Synthesis of Some Novel Triazole Derivatives and Their Biological Activity. Russ J Gen Chem 2021;91:1592-603. [DOI: 10.1134/s1070363221080235] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
28 Jablasone ST Jr, Ye Z, Duan S, Xu ZF, Li CY. Synthesis of benzothiazonine by rhodium-catalyzed denitrogenative transannulation of 1-sulfonyl-1,2,3-triazole and thiochromone. Org Biomol Chem 2021;19:5758-61. [PMID: 34124725 DOI: 10.1039/d1ob00419k] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
29 Liang T, Sun X, Li W, Hou G, Gao F. 1,2,3-Triazole-Containing Compounds as Anti-Lung Cancer Agents: Current Developments, Mechanisms of Action, and Structure-Activity Relationship. Front Pharmacol 2021;12:661173. [PMID: 34177578 DOI: 10.3389/fphar.2021.661173] [Cited by in Crossref: 15] [Cited by in F6Publishing: 17] [Article Influence: 7.5] [Reference Citation Analysis]
30 Efremova MM, Govdi AI, Frolova VV, Rumyantsev AM, Balova IA. Design and Synthesis of New 5-aryl-4-Arylethynyl-1H-1,2,3-triazoles with Valuable Photophysical and Biological Properties. Molecules 2021;26:2801. [PMID: 34068559 DOI: 10.3390/molecules26092801] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
31 Gaber A, Alsanie WF, de Farias RF, Refat MS. Preparation and Thermogravimetric and Antimicrobial Investigation of Cd (II) and Sn (II) Adducts of Mercaptopyridine, Amino Triazole Derivatives, and Mercaptothiazoline Organic Ligand Moieties. Bioinorg Chem Appl 2021;2021:6638229. [PMID: 33953737 DOI: 10.1155/2021/6638229] [Reference Citation Analysis]
32 Tan Z, Deng J, Ye Q, Zhang Z. Triazole-containing hybrids with anti-Mycobacterium tuberculosis potential - Part I: 1,2,3-Triazole. Future Med Chem 2021;13:643-62. [PMID: 33619989 DOI: 10.4155/fmc-2020-0301] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
33 Moghimi S, Salarinejad S, Toolabi M, Firoozpour L, Esmaeil Sadat Ebrahimi S, Safari F, Madani-Qamsari F, Mojtabavi S, Faramarzi MA, Karima S, Pakrad R, Foroumadi A. Synthesis, in-vitro evaluation, molecular docking, and kinetic studies of pyridazine-triazole hybrid system as novel α-glucosidase inhibitors. Bioorg Chem 2021;109:104670. [PMID: 33588241 DOI: 10.1016/j.bioorg.2021.104670] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
34 Sun Y, Wang Z, Wang Y, Xu T, Tian K, Zhang P. Synthesis and Antimicrobial Activity of 1,5-Benzothiazepines Incorporated with Triazole Moiety. Chinese Journal of Organic Chemistry 2021;41:2361. [DOI: 10.6023/cjoc202012044] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
35 El Malah T, Soliman HA, Hemdan BA, Abdel Mageid RE, Nour HF. Synthesis and antibiofilm activity of 1,2,3-triazole-pyridine hybrids against methicillin-resistant Staphylococcus aureus (MRSA). New J Chem 2021;45:10822-30. [DOI: 10.1039/d1nj00773d] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
36 Gao Y, Chen Y, Cao Y, Mo A, Peng Q. Potentials of nanotechnology in treatment of methicillin-resistant Staphylococcus aureus. Eur J Med Chem 2021;213:113056. [PMID: 33280899 DOI: 10.1016/j.ejmech.2020.113056] [Cited by in Crossref: 39] [Cited by in F6Publishing: 38] [Article Influence: 13.0] [Reference Citation Analysis]
37 Lima YR, Da Costa GP, Xavier MCDF, De Moraes MC, Barcellos T, Alves D, Silva MS. Synthesis of α ‐Hydroxyphosphonates Containing Functionalized 1,2,3‐Triazoles. ChemistrySelect 2020;5:12487-93. [DOI: 10.1002/slct.202003761] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]