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For: Aggarwal R, Sumran G. An insight on medicinal attributes of 1,2,4-triazoles. Eur J Med Chem 2020;205:112652. [PMID: 32771798 DOI: 10.1016/j.ejmech.2020.112652] [Cited by in Crossref: 26] [Cited by in F6Publishing: 12] [Article Influence: 13.0] [Reference Citation Analysis]
Number Citing Articles
1 Aggarwal R, Hooda M, Kumar P, Sumran G. Vision on Synthetic and Medicinal Facets of 1,2,4-Triazolo[3,4-b][1,3,4]thiadiazine Scaffold. Top Curr Chem (Cham) 2022;380:10. [PMID: 35122161 DOI: 10.1007/s41061-022-00365-x] [Reference Citation Analysis]
2 Eya’ane Meva F, Prior TJ, Evans DJ, Shah S, Tamngwa CF, Belengue HGL, Mang RE, Munro J, Qahash T, Llinás M. Anti-inflammation and antimalarial profile of 5-pyridin-2-yl-1H-[1,2,4]triazole-3-carboxylic acid ethyl ester as a low molecular intermediate for hybrid drug synthesis. Res Chem Intermed 2022;48:885-98. [DOI: 10.1007/s11164-021-04607-3] [Reference Citation Analysis]
3 Zhou LN, Feng FF, Cheung CW, Ma JA. Cu-Enabled [3 + 2] Annulation of In Situ Formed Nitrile Ylides with Aryldiazonium Salts: Access to 5-Cyano-1,2,4-Triazoles. Org Lett 2021;23:739-44. [PMID: 33428426 DOI: 10.1021/acs.orglett.0c03960] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Shahid W, Ashraf M, Saleem M, Bashir B, Muzaffar S, Ali M, Kaleem A, Aziz-Ur-Rehman, Amjad H, Bhattarai K, Riaz N. Exploring phenylcarbamoylazinane-1,2,4-triazole thioethers as lipoxygenase inhibitors supported with in vitro, in silico and cytotoxic studies. Bioorg Chem 2021;115:105261. [PMID: 34416506 DOI: 10.1016/j.bioorg.2021.105261] [Reference Citation Analysis]
5 Batalha PN, Mocanu T, Calancea S, Vaz MG, Andruh M. Zinc(II) and copper(II) complexes constructed from new bis(1H-1,2,3-triazole-4-carboxylate)-based ligands. Journal of Molecular Structure 2022;1259:132703. [DOI: 10.1016/j.molstruc.2022.132703] [Reference Citation Analysis]
6 Pirota V, Benassi A, Doria F. Lights on 2,5-diaryl tetrazoles: applications and limits of a versatile photoclick reaction. Photochem Photobiol Sci. [DOI: 10.1007/s43630-022-00173-8] [Reference Citation Analysis]
7 Al-Wahaibi LH, Rahul B, Mohamed AAB, Abdelbaky MSM, Garcia-Granda S, El-Emam AA, Percino MJ, Thamotharan S. Supramolecular Self-Assembly Built by Weak Hydrogen, Chalcogen, and Unorthodox Nonbonded Motifs in 4-(4-Chlorophenyl)-3-[(4-fluorobenzyl)sulfanyl]-5-(thiophen-2-yl)-4H-1,2,4-triazole, a Selective COX-2 Inhibitor: Insights from X-ray and Theoretical Studies. ACS Omega 2021;6:6996-7007. [PMID: 33748613 DOI: 10.1021/acsomega.0c06287] [Reference Citation Analysis]
8 Singh K, Kumari B, Sharma A. Copper(II), nickel(II), zinc(II) and cadmium(II) complexes of 1,2,4-triazole based Schiff base ligand: synthesis, comparative spectroscopic, thermal, biological and molecular docking studies. Spectroscopy Letters 2021;54:742-62. [DOI: 10.1080/00387010.2021.1996395] [Reference Citation Analysis]
9 Gumus MK, Sen F, Kansiz S, Dege N, Saif E. Crystal structure and Hirshfeld surface analysis of 2-{[(E)-(3-cyclo-butyl-1H-1,2,4-triazol-5-yl)imino]-meth-yl}phenol. Acta Crystallogr E Crystallogr Commun 2021;77:1267-71. [PMID: 34925895 DOI: 10.1107/S2056989021011658] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Zheng L, Tao K, Zhuo X, Xie Z, Liu G, Deng L, Mei W, Zou X, Zhong Y, Wu Y, Guo W. Photocatalytic Three‐Component Tandem Annulation Access to Multiply Substituted 1,2,4‐Triazole‐3,5‐diamines. Asian J of Organic Chemis 2021;10:3034-8. [DOI: 10.1002/ajoc.202100444] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Zengin M, Unsal Tan O, Arafa RK, Balkan A. Design and Synthesis of New 2-Oxoquinoxalinyl-1,2,4-triazoles as Antitumor VEGFR-2 Inhibitors. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.105696] [Reference Citation Analysis]
12 Wani AA, Chourasiya SS, Kathuria D, Sahoo SC, Beifuss U, Bharatam PV. Iodine Catalyzed Oxidative Coupling of Diaminoazines and Amines for the Synthesis of 3,5-Disubstituted-1,2,4-Triazoles. J Org Chem 2021;86:7659-71. [PMID: 34003643 DOI: 10.1021/acs.joc.1c00704] [Reference Citation Analysis]
13 Liu J, Liang Q, Li J, Xiao L. Crystal structure of ( E )-(2-methoxy-benzylidene)-(4-[1,2,4]triazol-1-yl-phenyl)-amine, C 16 H 14 N 4 O. Zeitschrift für Kristallographie - New Crystal Structures 2022;0. [DOI: 10.1515/ncrs-2021-0479] [Reference Citation Analysis]
14 Luan M, Xu Y, Zhang X, Li D, Yan M, Hou G, Meng Q, Zhao F, Zhao F. Design and synthesis of novel aza-ursolic acid derivatives: in vitro cytotoxicity and nitric oxide release inhibitory activity. Future Med Chem 2022. [PMID: 35286228 DOI: 10.4155/fmc-2021-0319] [Reference Citation Analysis]
15 Wang Y, Liu D. An Important Potential Anti-Epileptic/Anticonvulsant Active Group: A Review of 1,2,4-Triazole Groups and Their Action. Drug Res (Stuttg) 2021. [PMID: 34758502 DOI: 10.1055/a-1670-6992] [Reference Citation Analysis]
16 Blokhina SV, Sharapova AV, Ol'khovich MV, Doroshenko IA, Levshin IB, Perlovich GL. Synthesis and antifungal activity of new hybrids thiazolo[4,5-d]pyrimidines with (1H-1,2,4)triazole. Bioorg Med Chem Lett 2021;40:127944. [PMID: 33713781 DOI: 10.1016/j.bmcl.2021.127944] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Tsaplin GV, Popkov SV. Intramolecular ANRORC Reactions in the Series of Diazoles with Three Heteroatoms. Russ J Org Chem 2022;58:1-14. [DOI: 10.1134/s1070428022010018] [Reference Citation Analysis]
18 An S, Meng S, Xue J, Wang H, Zheng X, Zhao Y. UV-Vis, Raman spectroscopic and density functional theoretical studies on microsolvation 1, 2, 4-triazole-3-thione clusters. Spectrochim Acta A Mol Biomol Spectrosc 2021;258:119762. [PMID: 33930854 DOI: 10.1016/j.saa.2021.119762] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Cao Y, Lu H. Advances in the application of 1,2,4-triazole-containing hybrids as anti-tuberculosis agents. Future Med Chem 2021;13:2107-24. [PMID: 34698509 DOI: 10.4155/fmc-2020-0295] [Reference Citation Analysis]
20 Liu X, Liu H, Bian C, Wang KH, Wang J, Huang D, Su Y, Lv X, Hu Y. Synthesis of 3-Trifluoromethyl-1,2,4-triazolines and 1,2,4-Triazoles via Tandem Addition/Cyclization of Trifluoromethyl N-Acylhydrazones with Cyanamide. J Org Chem 2022. [PMID: 35412831 DOI: 10.1021/acs.joc.2c00176] [Reference Citation Analysis]
21 Sun S, Yan J, Tai L, Chai J, Hu H, Han L, Lu A, Yang C, Chen M. Novel (Z)/(E)-1,2,4-triazole derivatives containing oxime ether moiety as potential ergosterol biosynthesis inhibitors: design, preparation, antifungal evaluation, and molecular docking. Mol Divers 2022. [PMID: 35290557 DOI: 10.1007/s11030-022-10412-w] [Reference Citation Analysis]
22 Xu H, Cao C, Wang X, Guo MB, Yan ZZ, An R, Zhang R, Dong EH, Mou YH, Hou Z, Guo C. Discovery of 1,2,3-selenadiazole analogues as antifungal agents using a scaffold hopping approach. Bioorg Chem 2021;115:105182. [PMID: 34333426 DOI: 10.1016/j.bioorg.2021.105182] [Reference Citation Analysis]
23 El‐sebaey SA. Recent Advances in 1,2,4‐Triazole Scaffolds as Antiviral Agents. ChemistrySelect 2020;5:11654-80. [DOI: 10.1002/slct.202002830] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 3.5] [Reference Citation Analysis]
24 Azim T, Wasim M, Akhtar MS, Akram I. An in vivo evaluation of anti-inflammatory, analgesic and anti-pyretic activities of newly synthesized 1, 2, 4 Triazole derivatives. BMC Complement Med Ther 2021;21:304. [PMID: 34972515 DOI: 10.1186/s12906-021-03485-x] [Reference Citation Analysis]
25 El Ashry ESH, Farahat MM, Awad LF, Balbaa M, Yusef H, Badawy ME, Abd Al Moaty MN. New 4-(arylidene)amino-1,2,4-traizole-5-thiol derivatives and their acyclo thioglycosides as α-glucosidase and α-amylase inhibitors: Design, synthesis, and molecular modelling studies. Journal of Molecular Structure 2022;1259:132733. [DOI: 10.1016/j.molstruc.2022.132733] [Reference Citation Analysis]
26 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] [Reference Citation Analysis]
27 Sukhanov GT, Filippova YV, Gatilov YV, Sukhanova AG, Bosov KK, Krupnova IA, Pivovarova EV. Acidic N-dealkylation in nitrotriazolium salts. Mendeleev Communications 2022;32:215-7. [DOI: 10.1016/j.mencom.2022.03.020] [Reference Citation Analysis]
28 Bekircan O, Danış Ö, Şahin ME, Çetin M. Monoamine oxidase A and B inhibitory activities of 3,5-diphenyl-1,2,4-triazole substituted [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole derivatives. Bioorg Chem 2022;118:105493. [PMID: 34814086 DOI: 10.1016/j.bioorg.2021.105493] [Reference Citation Analysis]
29 Al-Hussain SA, Farghaly TA, Zaki MEA, Abdulwahab HG, Al-Qurashi NT, Muhammad ZA. Discovery of novel indolyl-1,2,4-triazole hybrids as potent vascular endothelial growth factor receptor-2 (VEGFR-2) inhibitors with potential anti-renal cancer activity. Bioorg Chem 2020;105:104330. [PMID: 33038552 DOI: 10.1016/j.bioorg.2020.104330] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
30 Zhang XH, Kang HQ, Tao YY, Li YH, Zhao JR, Ya-Gao, Ma LY, Liu HM. Identification of novel 1,3-diaryl-1,2,4-triazole-capped histone deacetylase 6 inhibitors with potential anti-gastric cancer activity. Eur J Med Chem 2021;218:113392. [PMID: 33831778 DOI: 10.1016/j.ejmech.2021.113392] [Reference Citation Analysis]
31 Modak A, Alegre-Requena JV, de Lescure L, Rynders KJ, Paton RS, Race NJ. Homologation of Electron-Rich Benzyl Bromide Derivatives via Diazo C-C Bond Insertion. J Am Chem Soc 2021. [PMID: 34898193 DOI: 10.1021/jacs.1c11503] [Reference Citation Analysis]
32 Khaliullin FA, Nikitina IL, Klen EE, Miftakhova AF, Makarova NN, Gabidullin RA, Gilmanova AG. Synthesis and Antidepressant Activity of 4-Alkyl-5-Bromo-2,4-Dihydro-2-(Thietan-3-YL)-1,2,4-Triazol-3-Ones. Pharm Chem J 2021;55:123-9. [DOI: 10.1007/s11094-021-02394-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Singer RA, Monfette S, Bernhardson D, Tcyrulnikov S, Hubbell AK, Hansen EC. Recent Advances in Nonprecious Metal Catalysis. Org Process Res Dev 2021;25:1802-15. [DOI: 10.1021/acs.oprd.1c00241] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
34 Budeev A, Kantin G, Dar'in D, Krasavin M. Diazocarbonyl and Related Compounds in the Synthesis of Azoles. Molecules 2021;26:2530. [PMID: 33926128 DOI: 10.3390/molecules26092530] [Reference Citation Analysis]