共 30 条
[1]
Ang J.Y., Ezike, Asmar B.I., Antibacterial resistance, Indian J. Pediatr, 71, pp. 229-239, (2004)
[2]
Reygaert W.C., An overview of the antimicrobial resistance mechanisms of bacteria, AIMS Microbiol, 4, pp. 482-501, (2018)
[3]
Gunasekera S.P., Cross S.S., Fistularin 3 and 11-ketofistularin 3. Feline leukemia virus active bromotyrosine metabolites from the marine sponge Aplysina archeri, J. Nat. Prod, 55, pp. 509-512, (1992)
[4]
Gahlot U.S., Rao S.S., Jhala Y.S., Dulawat S.S., Verma B.L., Microwave assisted synthesis and antibacterial activity of some new 3,5-diaryl-2-isoxazolines, Indian J. Heterocycl, 13, pp. 111-114, (2003)
[5]
Sadashiva M.P., Mantelingu K., Swamy S.N., Rangappa K.S., Solution-phase synthesis of novel Δ2-isoxazoline libraries via 1, 3-dipolar cycloaddition and their antifungal properties, Bioorg. Med. Chem, 11, pp. 4539-4544, (2003)
[6]
Huang S., Ma H., Wang Z., Zhang P., Li S., Li Y., Liu A., Li Y., Liu Y., Wang Q., Design, synthesis, and insecticidal and fungicidal activities of ether/oxime-ether containing isoxazoline derivatives, Indian J. Heterocycl, 71, pp. 5107-5116, (2023)
[7]
Gao Y.C., Song X., Jia T., Zhao C., Yao G., Xu H., Discovery of new N-Phenylamide Isoxazoline derivatives with high insecticidal activity and reduced honeybee toxicity, Pestic. Biochem. Physiol, 200, (2024)
[8]
Kaur K., Kumar V., Sharma A.K., Gupta G.K., Isoxazoline containing natural products as anticancer agents: A review, Eur. J. Med. Chem, 77, pp. 121-133, (2014)
[9]
Ahmad A., Ahmad A., Varshney H., Rauf A., Rehan M., Subbarao N., Khan A.U., Designing and synthesis of novel antimicrobial heterocyclic analogs of fatty acids, Eur. J. Med. Chem, 70, pp. 887-900, (2013)
[10]
Tangallapally R.P., Sun D., Budha N., Lee R.E., Lenaerts A.J., Meibohm B., Lee R.E., Discovery of novel isoxazolines as anti-tuberculosis agents, Bioorg. Med. Chem. Lett, 17, pp. 6638-6642, (2007)