Design, synthesis and molecular docking studies of some 1-(5-(2-fluoro-5-(trifluoromethoxy)phenyl)-1,2,4-oxadiazol-3-yl)piperazine derivatives as potential anti-inflammatory agents

[11] Sipahi H(2017)Chemistry of 1,2,3-triazoles: biological properties of 1 Eur J Med Chem 139 665-8560

[12] Bozkurt A(2021)Design, synthesis, molecular docking, and anticancer activity of benzoxazole derivatives as VEGFR-2 inhibitors Bioorg Med Chem 42 116266-2325

[13] Bilge SS(2021)Click triazoles as chemosensors New J Chem 45 11136-4301

[14] Rho T(2018)Assembly of new heterocycles through an effective use of bisaldehydes by using a sequential GBB/Ugi reaction J Braz Chem Soc 29 435-880

[15] Jeong HW(2014)Arylthiazole antibiotics targeting intracellular methicillin-resistant Staphylococcus aureus (MRSA) that interfere with bacterial cell wall synthesis Drug Res 64 66-117

[16] Hong YD(2020)From triazolophthalazines to triazoloquinazolines: a bioisosterism-guided approach toward the identification of novel PCAF inhibitors with potential anticancer activity Arch. Pharm. 353 e2000061-29

[17] Yoon K(2017)1,2,4-Triazolo[4,3- RSC Adv 7 8550-1498

[18] Cho JY(2017)]quinazolines: a bioisosterism-guided approach towards the development of novel PCAF inhibitors with potential anticancer activity J Heterocycl Chem 54 2319-1875

[19] Yoon KD(2020)1,2,4- and 1,3,4-oxadiazoles as scaffolds in the development of antiparasitic agents Bioorg Chem 94 103364-1163

[20] Blobaum AL(2017)Synthesis and anti-inflammatory activities of novel 5-(3,4-dichlorophenyl)-3-[(4-substitutedpiperazin-1-yl)methyl]-1,3,4-oxadiaxole-2(3 Bioorg Med Chem Lett 27 4298-5233

[11] Sipahi H(2017)Chemistry of 1,2,3-triazoles: biological properties of 1 Eur J Med Chem 139 665-8560

[12] Bozkurt A(2021)Design, synthesis, molecular docking, and anticancer activity of benzoxazole derivatives as VEGFR-2 inhibitors Bioorg Med Chem 42 116266-2325

[13] Bilge SS(2021)Click triazoles as chemosensors New J Chem 45 11136-4301

[14] Rho T(2018)Assembly of new heterocycles through an effective use of bisaldehydes by using a sequential GBB/Ugi reaction J Braz Chem Soc 29 435-880

[15] Jeong HW(2014)Arylthiazole antibiotics targeting intracellular methicillin-resistant Staphylococcus aureus (MRSA) that interfere with bacterial cell wall synthesis Drug Res 64 66-117

[16] Hong YD(2020)From triazolophthalazines to triazoloquinazolines: a bioisosterism-guided approach toward the identification of novel PCAF inhibitors with potential anticancer activity Arch. Pharm. 353 e2000061-29

[17] Yoon K(2017)1,2,4-Triazolo[4,3- RSC Adv 7 8550-1498

[18] Cho JY(2017)]quinazolines: a bioisosterism-guided approach towards the development of novel PCAF inhibitors with potential anticancer activity J Heterocycl Chem 54 2319-1875

[19] Yoon KD(2020)1,2,4- and 1,3,4-oxadiazoles as scaffolds in the development of antiparasitic agents Bioorg Chem 94 103364-1163

[20] Blobaum AL(2017)Synthesis and anti-inflammatory activities of novel 5-(3,4-dichlorophenyl)-3-[(4-substitutedpiperazin-1-yl)methyl]-1,3,4-oxadiaxole-2(3 Bioorg Med Chem Lett 27 4298-5233