BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Gao F, Ye L, Kong F, Huang G, Xiao J. Design, synthesis and antibacterial activity evaluation of moxifloxacin-amide-1,2,3-triazole-isatin hybrids. Bioorg Chem 2019;91:103162. [PMID: 31382058 DOI: 10.1016/j.bioorg.2019.103162] [Cited by in Crossref: 25] [Cited by in F6Publishing: 26] [Article Influence: 6.3] [Reference Citation Analysis]
Number Citing Articles
1 Gao J, Hou H, Gao F. Current scenario of quinolone hybrids with potential antibacterial activity against ESKAPE pathogens. Eur J Med Chem 2023;247:115026. [PMID: 36577217 DOI: 10.1016/j.ejmech.2022.115026] [Reference Citation Analysis]
2 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]
3 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]
4 Pedrood K, Azizian H, Montazer MN, Moazzam A, Asadi M, Montazeri H, Biglar M, Zamani M, Larijani B, Zomorodian K, Mohammadi-Khanaposhtani M, Irajie C, Amanlou M, Iraji A, Mahdavi M. Design and synthesis of new N-thioacylated ciprofloxacin derivatives as urease inhibitors with potential antibacterial activity. Sci Rep 2022;12:13827. [PMID: 35970866 DOI: 10.1038/s41598-022-17993-4] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Chowdhary S, Shalini, Arora A, Kumar V. A Mini Review on Isatin, an Anticancer Scaffold with Potential Activities against Neglected Tropical Diseases (NTDs). Pharmaceuticals 2022;15:536. [DOI: 10.3390/ph15050536] [Reference Citation Analysis]
6 Pan J, Ma L, Tang Y, Tian Y, Lin Y, Zhang L, Gao F, Lu G. Design, Synthesis and Biological evaluation of novel Quinazoline Derivatives as potential NF-κb inhibitors. Arabian Journal of Chemistry 2022. [DOI: 10.1016/j.arabjc.2022.103908] [Reference Citation Analysis]
7 Cheke RS, Patil VM, Firke SD, Ambhore JP, Ansari IA, Patel HM, Shinde SD, Pasupuleti VR, Hassan MI, Adnan M, Kadri A, Snoussi M. Therapeutic Outcomes of Isatin and Its Derivatives against Multiple Diseases: Recent Developments in Drug Discovery. Pharmaceuticals 2022;15:272. [DOI: 10.3390/ph15030272] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
8 Cebeci YU, Ceylan Ş, Karaoğlu ŞA. Conventional and microwave irradiated synthesis, biological activity evaluation of highly substituted indole-triazole hybrids. Journal of Molecular Structure 2022;1250:131799. [DOI: 10.1016/j.molstruc.2021.131799] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Malah TE, Farag H, Hemdan BA, Abdel Mageid RE, Abdelrahman MT, El-manawaty MA, Nour HF. Synthesis, in vitro antimicrobial evaluation, and molecular docking studies of new isatin-1,2,3-triazole hybrids. Journal of Molecular Structure 2022;1250:131855. [DOI: 10.1016/j.molstruc.2021.131855] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
10 Moura NM, Tomé AC. 1,2,3-Triazoles. Comprehensive Heterocyclic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-818655-8.00067-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Kumar L, Lal K, Kumar A, Paul AK, Kumar A. Pyrazoline tethered 1,2,3-triazoles: Synthesis, antimicrobial evaluation and in silico studies. Journal of Molecular Structure 2021;1246:131154. [DOI: 10.1016/j.molstruc.2021.131154] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
12 Jenifer VR, Muthuvel P, Das TM. Rational Design of Heterocyclic Moieties Incorporated in [1,2,3]Sugar‐Triazole Derivatives for Antioxidant Studies. ChemistrySelect 2021;6:9955-9. [DOI: 10.1002/slct.202102516] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
13 Wen X, Almousa R, Na S, Anderson GG, Xie D. Polyurethane coated with polyvinylpyrrolidones via triazole links for enhanced surface fouling resistance. Biosurface and Biotribology 2021;7:219-27. [DOI: 10.1049/bsb2.12023] [Reference Citation Analysis]
14 Jia Y, Zhao L. The antibacterial activity of fluoroquinolone derivatives: An update (2018-2021). Eur J Med Chem 2021;224:113741. [PMID: 34365130 DOI: 10.1016/j.ejmech.2021.113741] [Cited by in Crossref: 10] [Cited by in F6Publishing: 14] [Article Influence: 5.0] [Reference Citation Analysis]
15 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]
16 Sai Allaka B, Basavoju S, Rama Krishna G. A Photoinduced Multicomponent Regioselective Synthesis of 1,4,5‐Trisubstituted‐1,2,3‐Triazoles: Transition Metal‐, Azide‐ and Oxidant‐Free Protocol. Adv Synth Catal 2021;363:3560-5. [DOI: 10.1002/adsc.202100321] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
17 Almousa R, Wen X, Anderson G, Xie D. PVP ‐coated PVC with triazoles for reduced cell adhesion and bacterial growth. Polymers for Advanced Techs 2021;32:4126-34. [DOI: 10.1002/pat.5420] [Reference Citation Analysis]
18 Yang M, Liu H, Zhang Y, Wang X, Xu Z. Moxifloxacin-isatin Hybrids Tethered by 1,2,3-triazole and their Anticancer Activities. Curr Top Med Chem 2020;20:1461-7. [PMID: 31994464 DOI: 10.2174/1568026620666200128144825] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
19 Amin NH, El-Saadi MT, Ibrahim AA, Abdel-Rahman HM. Design, synthesis and mechanistic study of new 1,2,4-triazole derivatives as antimicrobial agents. Bioorg Chem 2021;111:104841. [PMID: 33798851 DOI: 10.1016/j.bioorg.2021.104841] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
20 Nural Y, Ozdemir S, Doluca O, Demir B, Yalcin MS, Atabey H, Kanat B, Erat S, Sari H, Seferoglu Z. Synthesis, biological properties, and acid dissociation constant of novel naphthoquinone–triazole hybrids. Bioorganic Chemistry 2020;105:104441. [DOI: 10.1016/j.bioorg.2020.104441] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
21 Huang G, Solano CM, Melendez J, Yu-Alfonzo S, Boonhok R, Min H, Miao J, Chakrabarti D, Yuan Y. Discovery of fast-acting dual-stage antimalarial agents by profiling pyridylvinylquinoline chemical space via copper catalyzed azide-alkyne cycloadditions. Eur J Med Chem 2021;209:112889. [PMID: 33045660 DOI: 10.1016/j.ejmech.2020.112889] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
22 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]
23 Awolade P, Cele N, Kerru N, Singh P. Synthesis, antimicrobial evaluation, and in silico studies of quinoline-1H-1,2,3-triazole molecular hybrids. Mol Divers 2021;25:2201-18. [PMID: 32507981 DOI: 10.1007/s11030-020-10112-3] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 4.0] [Reference Citation Analysis]
24 Radwan NH, Nasr M, Ishak RAH, Abdeltawab NF, Awad GAS. Chitosan-calcium phosphate composite scaffolds for control of post-operative osteomyelitis: Fabrication, characterization, and in vitro-in vivo evaluation. Carbohydr Polym 2020;244:116482. [PMID: 32536391 DOI: 10.1016/j.carbpol.2020.116482] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 7.3] [Reference Citation Analysis]
25 Koshelev VN, Primerova OV, Vorobyev SV, Ivanova LV. Synthesis, Redox Properties and Antibacterial Activity of Hindered Phenols Linked to Heterocycles. Molecules 2020;25:E2370. [PMID: 32443779 DOI: 10.3390/molecules25102370] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
26 Prayitno B, Santoso M. Biochemical activities of new isatin derivative against WiDr colon cancer. J Phys : Conf Ser 2020;1422:012017. [DOI: 10.1088/1742-6596/1422/1/012017] [Reference Citation Analysis]