Warianty tytułu
Języki publikacji
Abstrakty
A series of novel triazolo[1,5-a]pyrimidine derivatives was synthesized from 5-amino-1,2,4-triazole and biologically active morpholinone amine in excellent yield as promising class of antimicrobial agents. The antimicrobial activities were investigated against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus pyogen, Candida albicans, Aspergillusniger, Aspergillusclavatus and compared with standard drugs Ampicillin, Chloramphenicol, Norfloxacin and Griseofulvin. All the synthesized compounds were characterized by IR, 1H NMR, 13C and mass spectroscopy. The result of antimicrobial activity data revealed that compound 4f,4g and 4i were found more active against bacterial species and compound 4c, 4d, 4g, 4i and 4jwere found more active against fungal strain, while other compounds shows moderate to law activity against microbes.
Rocznik
Tom
Strony
12--21
Opis fizyczny
Bibliogr. 24 poz., tab., wz.
Twórcy
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India, naliaparachem@yahoo.com
Bibliografia
- [1] Fischer G., Adv. Heterocyclic Chemistry 57 (1993) 81.
- [2] Shaban M. A. E., Morgan A. E. A., Adv. Heterocyclic Chemistry 77 (2000) 345.
- [3] Shaban, M. A. E., Morgan A. E. A., Adv. Heterocyclic Chemistry 73 (2000) 131.
- [4] Shaban, M. A. E.; Morgan A. E. A., Adv. Heterocyclic Chemistry 75 (2000) 243.
- [5] Ashour H. M., Shaaban O. G., Rizk O. H., El-Ashmawy I. M., Euro. J. Med. Chem. 62 (2013) 341.
- [6] Marwaha A., White J., El Mazoun F., Creason S. A., Kokkond S., Buckner F. S., Rathod P. K., J. Med. Chem. 55 (2012) 7425.
- [7] Chen Q., Zhu X. L., Liu, et al., Euro. J. Med. Chem. 43 (2008) 595.
- [8] Uryu S., Tokuhiro S., Murasugi T., Brain Research 946 (2002) 298.
- [9] Zhang N., Semiramis A. K., Thai N., J. Med. Chem. 50 (2007) 319.
- [10] Havlicek L., Fuksova K., Krystof V., Bioorg. Med. Chem. 13 (2005) 5399.
- [11] Zhao X., Zhao Y., Guo S., Song H., Wang D., Gong P., Molecules 12 (2007) 1136.
- [12] Iwona L., Marzena F., Tadeusz M., Tadeusz S., Julia J., Dalton Transactions 42 (2013) 6219.
- [13] Yin L., Shuai Z., Zhi-Jun L., Hai-Liang Z., Euro. J. Med. Chem. 64 (2013) 54.
- [14] Ashraf H. F., Abd El-Wahab, Pharmaceuticals 5 (2012) 745.
- [15] Abdel-Aziem A., Sayed El-Gendy M., Abdelhamid A. O., Euro. J. Chem. 3 (2012) 455.
- [16] Khera M. K., Cliffe I. A., Mathur T., Prakash O., Bioorg & Med. Chem. Lett. 21 (2011) 2887.
- [17] Fraley M. E., Hoffman W. F., Rubino R. S., Bioorg. Med. Chem. Lett. 12 (2002) 2767.
- [18] Antonino L., Ilenia A., Chiara P., Annamaria M., Gaetano D., Maria A. A., Euro. J. Med. Chem. 62 (2013) 416.
- [19] Fairfield B. J., Andrew C., Allan J., WO2004108136, 2004.
- [20] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
- [21] Nirav M. Shah, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 6 (2014) 56-60.
- [22] Piyush B. Vekariya, Jalpa R. Pandya, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 7 (2014) 45-52.
- [23] Sagar P. Gami, Kalpesh V. Vilapara, Hasmukh R. Khunt, Jayesh S. Babariya, Yogesh T. Naliapara, International Letters of Chemistry, Physics and Astronomy 11(2) (2014) 127-134.
- [24] Hasmukh R. Khunt, Piyush P. Pipaliya, Satish M. Ghelani, Jayesh S. Babariya, Yogesh T. Naliapara, International Letters of Chemistry, Physics and Astronomy 12 (2014) 20-25
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.baztech-fc0df2db-0910-4670-a98d-57cb37b779cc