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For: Benassi A, Doria F, Pirota V. Groundbreaking Anticancer Activity of Highly Diversified Oxadiazole Scaffolds. Int J Mol Sci 2020;21:E8692. [PMID: 33217987 DOI: 10.3390/ijms21228692] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Palumbo Piccionello A. Editorial for Special Issue "Bioactive Oxadiazoles". Int J Mol Sci 2021;22:3988. [PMID: 33924410 DOI: 10.3390/ijms22083988] [Reference Citation Analysis]
2 Khallaf A, Wang P, Zhuo S, Zhu H, Liu H. Synthesis, insecticidal activities, and structure–activity relationships of 1,3,4‐oxadiazole‐ring‐containing pyridylpyrazole‐4‐carboxamides as novel insecticides of the anthranilic diamide family. J Heterocyclic Chem 2021;58:2189-202. [DOI: 10.1002/jhet.4346] [Reference Citation Analysis]
3 Stecoza CE, Nitulescu GM, Draghici C, Caproiu MT, Olaru OT, Bostan M, Mihaila M. Synthesis and Anticancer Evaluation of New 1,3,4-Oxadiazole Derivatives. Pharmaceuticals (Basel) 2021;14:438. [PMID: 34066442 DOI: 10.3390/ph14050438] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
4 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]
5 Al-Wahaibi LH, Mohamed AAB, Tawfik SS, Hassan HM, El-Emam AA. 1,3,4-Oxadiazole N-Mannich Bases: Synthesis, Antimicrobial, and Anti-Proliferative Activities. Molecules 2021;26:2110. [PMID: 33916955 DOI: 10.3390/molecules26082110] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Khanfar MA. Oxadiazol-based mTOR inhibitors with potent antiproliferative activities: synthetic and computational modeling. Mol Divers 2022. [PMID: 34985718 DOI: 10.1007/s11030-021-10367-4] [Reference Citation Analysis]
7 Banik BK, Sahoo BM, Kumar BVVR, Panda KC, Jena J, Mahapatra MK, Borah P. Green Synthetic Approach: An Efficient Eco-Friendly Tool for Synthesis of Biologically Active Oxadiazole Derivatives. Molecules 2021;26:1163. [PMID: 33671751 DOI: 10.3390/molecules26041163] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Fray M, Elbini-dhouib I, Hamzi I, Doghri R, Srairi-abid N, Lesur D, Benazza M, Abidi R, Barhoumi-slimi T. Synthesis, characterization and in vivo antitumor effect of new α,β-unsaturated-2,5-disubstituted-1,3,4-oxadiazoles. Synthetic Communications. [DOI: 10.1080/00397911.2022.2053993] [Reference Citation Analysis]
9 Peng F, Liu T, Wang Q, Liu F, Cao X, Yang J, Liu L, Xie C, Xue W. Antibacterial and Antiviral Activities of 1,3,4-Oxadiazole Thioether 4H-Chromen-4-one Derivatives. J Agric Food Chem 2021;69:11085-94. [PMID: 34516137 DOI: 10.1021/acs.jafc.1c03755] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]