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For: Feng LS, Zheng MJ, Zhao F, Liu D. 1,2,3-Triazole hybrids with anti-HIV-1 activity. Arch Pharm (Weinheim) 2021;354:e2000163. [PMID: 32960467 DOI: 10.1002/ardp.202000163] [Cited by in Crossref: 30] [Cited by in F6Publishing: 33] [Article Influence: 10.0] [Reference Citation Analysis]
Number Citing Articles
1 Al-ghulikah H, Ghabi A, haouas A, Mtiraoui H, Jeanneau E, Msaddek M. Synthesis of new 1,2,3-triazole linked benzimidazolidinone : single crystal X-ray structure, biological activities evaluation and molecular docking studies. Arabian Journal of Chemistry 2023. [DOI: 10.1016/j.arabjc.2023.104566] [Reference Citation Analysis]
2 Kumar A, Lal K, Kumar V, Murtaza M, Jaglan S, Kumar Paul A, Yadav S, Kumari K. Synthesis, Antimicrobial, Antibiofilm and Computational studies of Isatin-Semicarbazone Tethered 1,2,3-Triazoles. Bioorganic Chemistry 2023. [DOI: 10.1016/j.bioorg.2023.106388] [Reference Citation Analysis]
3 Ribeiro JLP, Loureiro JB, Lopes SMM, Saraiva L, Pinho E Melo TMVD. 3-(1,2,3-Triazol-4-yl)-β-Carbolines and 3-(1H-Tetrazol-5-yl)-β-Carbolines: Synthesis and Evaluation as Anticancer Agents. Pharmaceuticals (Basel) 2022;15. [PMID: 36558961 DOI: 10.3390/ph15121510] [Reference Citation Analysis]
4 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]
5 Singh G, Saini A, Mohit, Pawan, Diksha, Sushma, Suman, Priyanka, Satija P. Elucidating the sensing properties of thiophene amended organosilane for detection of chromium(III) ion and its potential activity against HIV-1 RT via computational approach. Inorganic Chemistry Communications 2022;146:110090. [DOI: 10.1016/j.inoche.2022.110090] [Reference Citation Analysis]
6 El-sofany WI, El-sayed WA, Abd-rabou AA, El-shahat M. Synthesis of new imidazole-triazole-glycoside hybrids as anti-breast cancer candidates. Journal of Molecular Structure 2022;1270:133942. [DOI: 10.1016/j.molstruc.2022.133942] [Reference Citation Analysis]
7 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]
8 Deng C, Yan H, Wang J, Liu B, Liu K, Shi Y. The anti-HIV potential of imidazole, oxazole and thiazole hybrids: A mini-review. Arabian Journal of Chemistry 2022;15:104242. [DOI: 10.1016/j.arabjc.2022.104242] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Vala DP, Vala RM, Patel HM. Versatile Synthetic Platform for 1,2,3-Triazole Chemistry. ACS Omega. [DOI: 10.1021/acsomega.2c04883] [Reference Citation Analysis]
10 Deng C, Yan H, Wang J, Liu K, Liu B, Shi Y. Current scenario on non-nucleoside reverse transcriptase inhibitors (2018-present). Arabian Journal of Chemistry 2022. [DOI: 10.1016/j.arabjc.2022.104378] [Reference Citation Analysis]
11 Finke AO, Pavlova AV, Morozova EA, Tolstikova TG, Shults EE. Synthesis of 1,2,3-Triazolyl-Substituted Derivatives of the Alkaloids Sinomenine and Tetrahydrothebaine on Ring A and Their Analgesic Activity. Chem Nat Compd. [DOI: 10.1007/s10600-022-03824-5] [Reference Citation Analysis]
12 Ay E. Synthesis of new 1,2,3-triazolo-nucleoside analogues with 2-propargylamino pyrimidines via click reactions. Nucleosides, Nucleotides & Nucleic Acids 2022. [DOI: 10.1080/15257770.2022.2118317] [Reference Citation Analysis]
13 Yadav M, Lal K, Kumar A, Kumar A, Kumar D. Indole-chalcone linked 1,2,3-triazole hybrids: Facile synthesis, antimicrobial evaluation and docking studies as potential antimicrobial agents. Journal of Molecular Structure 2022;1261:132867. [DOI: 10.1016/j.molstruc.2022.132867] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Dhameja M, Kumar H, Kurella S, Uma A, Gupta P. Flavone-1,2,3-triazole derivatives as potential α-glucosidase inhibitors: Synthesis, enzyme inhibition, kinetic analysis and molecular docking study. Bioorg Chem 2022;127:106028. [PMID: 35868105 DOI: 10.1016/j.bioorg.2022.106028] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
15 Kariuki BM, Mohamed HA, Abdel-wahab BF, El-hiti GA. 4-((5-(1-(4-Fluorophenyl)-5-methyl-1 H -1,2,3-triazol-4-yl)-1,3,4-thiadiazol-2-yl)amino)benzenesulfonic acid: unexpected synthesis, structure elucidation and antimicrobial activity. Phosphorus, Sulfur, and Silicon and the Related Elements. [DOI: 10.1080/10426507.2022.2099858] [Reference Citation Analysis]
16 Jaiswal S, Devi M, Sharma N, Rathi K, Dwivedi J, Sharma S. Emerging Approaches for Synthesis of 1,2,3-Triazole Derivatives. A Review. Organic Preparations and Procedures International. [DOI: 10.1080/00304948.2022.2069456] [Reference Citation Analysis]
17 De Masi R, Orlando S. GANAB and N-Glycans Substrates Are Relevant in Human Physiology, Polycystic Pathology and Multiple Sclerosis: A Review. IJMS 2022;23:7373. [DOI: 10.3390/ijms23137373] [Reference Citation Analysis]
18 Albelwi FF, Abdu Mansour HM, Elshatanofy MM, El Kilany Y, Kandeel K, Elwakil BH, Hagar M, Aouad MR, El Ashry ESH, Rezki N, El Sawy MA. Design, Synthesis and Molecular Docking of Novel Acetophenone-1,2,3-Triazoles Containing Compounds as Potent Enoyl-Acyl Carrier Protein Reductase (InhA) Inhibitors. Pharmaceuticals 2022;15:799. [DOI: 10.3390/ph15070799] [Reference Citation Analysis]
19 Kumar A, Lal K, Poonia N, Kumar A, Kumar A. Synthesis, antimicrobial evaluation and docking studies of fluorinated imine linked 1,2,3-triazoles. Res Chem Intermed. [DOI: 10.1007/s11164-022-04737-2] [Reference Citation Analysis]
20 Sharma A, Agrahari AK, Rajkhowa S, Tiwari VK. Emerging impact of triazoles as anti-tubercular agent. Eur J Med Chem 2022;238:114454. [PMID: 35597009 DOI: 10.1016/j.ejmech.2022.114454] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Yang W, Xuan B, Li X, Si H, Chen A. Therapeutic potential of 1,2,3-triazole hybrids for leukemia treatment. Arch Pharm (Weinheim) 2022;:e2200106. [PMID: 35532286 DOI: 10.1002/ardp.202200106] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Ahmed Saleh Alzahrani S, Nazreen S, Elhenawy AA, Neamatallah T, Alam MM. Synthesis, Biological Evaluation, and Molecular Docking of New Benzimidazole-1,2,3-Triazole Hybrids as Antibacterial and Antitumor Agents. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2022.2069133] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Dong H, Wu J, Huo G. Design, synthesis and biological studies of some new imidazole-1,2,3-triazole hybrid derivatives. Journal of Molecular Structure 2022;1256:132516. [DOI: 10.1016/j.molstruc.2022.132516] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
24 Pogrebnoi S, Radul O, Stingaci E, Lupascu L, Valica V, Uncu L, Smetanscaia A, Petrou A, Ćirić A, Glamočlija J, Soković M, Geronikaki A, Macaev FZ. The Synthesis of Triazolium Salts as Antifungal Agents: A Biological and In Silico Evaluation. Antibiotics 2022;11:588. [DOI: 10.3390/antibiotics11050588] [Reference Citation Analysis]
25 El Sawy MA, Elshatanofy MM, El Kilany Y, Kandeel K, Elwakil BH, Hagar M, Aouad MR, Albelwi FF, Rezki N, Jaremko M, El Ashry ESH. Novel Hybrid 1,2,4- and 1,2,3-Triazoles Targeting Mycobacterium Tuberculosis Enoyl Acyl Carrier Protein Reductase (InhA): Design, Synthesis, and Molecular Docking. IJMS 2022;23:4706. [DOI: 10.3390/ijms23094706] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
26 A. El-hiti G, A. Mohamed H, F. Abdel-wahab B, Sabry E, M. Kariuki B. Synthesis and Antimicrobial Activity of 2,5-bis(Pyrazol-3-yl or Triazol-4-yl)-1,3,4-oxadiazoles. HETEROCYCLES 2022;104. [DOI: 10.3987/com-22-14676] [Reference Citation Analysis]
27 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]
28 Sekh TV, Shyyka OY, Pokhodylo NT, Obushak MD. Synthesis of 1H-1,2,3-triazole-4-carbonitriles as building blocks for promising 2-(triazol-4-yl)-thieno[2,3-d]pyrimidine drug candidates. Synthetic Communications 2021;51:3175-3186. [DOI: 10.1080/00397911.2021.1966041] [Reference Citation Analysis]
29 Talukdar R, Singh V, Mourya H, Nasibullah M, Tiwari B. Stitching Triazoles to Arenes via a Transition Metal-Free Aryne Diels-Alder/1,3-Prototropic Shift/Dehydrobromination Cascade. J Org Chem 2021;86:12277-84. [PMID: 34328329 DOI: 10.1021/acs.joc.1c00562] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
30 Shiri P, Amani AM, Mayer-Gall T. A recent overview on the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles. Beilstein J Org Chem 2021;17:1600-28. [PMID: 34354770 DOI: 10.3762/bjoc.17.114] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 6.0] [Reference Citation Analysis]
31 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]
32 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]
33 Sokolnikova TV, Proidakov AG, Kizhnyaev VN. Organocatalytic Enamine–Azide Addition Reaction in the Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles. Russ J Org Chem 2021;57:376-82. [DOI: 10.1134/s1070428021030088] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
34 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]
35 Xu Z, Chen Q, Zhang Y, Liang C. Coumarin-based derivatives with potential anti-HIV activity. Fitoterapia 2021;150:104863. [PMID: 33582266 DOI: 10.1016/j.fitote.2021.104863] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 10.5] [Reference Citation Analysis]