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Abstrakty
In this study some new o-benzimidazol-2'-yl-benzamido-p'-benzamido-2-phenyl-4-substituted phenyl-5-oxo-Imidazolines 3a-3j were synthesized. To synthesized target molecules we used various substituted oxazolone derivatives, synthesized from substituted benzaldehyde with hippuric acid. Substituted oxazolones 2a-2j were reacted with carbohydrazide derivative of benzimidazole 1 in presence of pyridine as base to obtained substituted imidazolinone derivatives. All synthesized compounds were characterized by IR, 1H NMR, elemental analysis and further supported by mass spectroscopy. All synthesized compounds were screened for their antimicrobial activity against gram positive and gram negative bacteria which showed moderate to good activity. All compounds showing good to moderate active against fungal strain as compare to standard drug.
Słowa kluczowe
Rocznik
Tom
Strony
74--80
Opis fizyczny
Bibliogr. 25 poz., tab., wykr.
Twórcy
autor
- Home Science Department, Dr. Subhash Mahila Arts, Commerce & Home Science College, Junagadh - 362 001, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
Bibliografia
- [1] Q. McKellar, E. Scott, J. Vet. Pharmacol. Ther. 13 (1990) 223.
- [2] A. Spasov, I. Yozhitsa, L. Bugaeva, V. Anisimova, Pharm. Chem. J. 33 (1999) 232.
- [3] J. Rossignol, H. Maisonneuve, Ann. Trop. Med. Parasitol. 78 (1984) 135.
- [4] A. Patil, S. Ganguly, S. Surana, Rasayan J. Chem. 1 (2008) 447.
- [5] A. Dubey, P. Sanyal, Online Vet. J. 5 (2010) 63.
- [6] M. Boiani, M. Gonzalez, Mini Rev. Med. Chem. 5 (2005) 409.
- [7] B. Narasimhan, D. Sharma, P. Kumar, Med. Chem. Res. 21 (2012) 269.
- [8] Duschinsky R. Imidazolone derivatives. US patent. 1995 US2707186.
- [9] D. Naithani, V. Srivastava, J. Barthwal, A. Saxena, T. Gupta, K. Shanker, Indian J Chem. 28B (1989) 990.
- [10] V. Kachhadia, M. Patel, H. Joshi, J. Serb. Chem. Soc. 70 (2005) 153.
- [11] M. Ding, G. Zeng G, Z. Liu, Phosphorus, Sulfur Silicon Relat. Elem. 177 (2002) 1315.
- [12] X. Huang, Z. Liu, F. Yang, M. Ding, Phosphorus, Sulfur Silicon Relat. Elem. 182 (2007) 939.
- [13] S. Demirayak, S. A. Karaburun, I. Kayagil, K. Erol, B. Sirmagul, Arch Pharm Res. 27 (2004) 13.
- [14] K.Thaker, P. Zalavadia, H. Joshi, Jour. of Science Islamic Repb. of Iran 16 (2005) 139.
- [15] A. Solankee, S. Solankee, G. Patel, Rasayan J Chem. 1 (2008) 228.
- [16] El-Sayed Ali T., Abdel-Aghfaar Abdel-Aziz S., Metwali El-Shaaer H., Ismail Hanafy F., Zaky El-Fauomy A., Turk J Chem. 32 (2008) 365.
- [17] R. Mistry, K. Desai, Eur Jour. Chem. 2 (2005) 42.
- [18] A. Bistrzycki, A. Lecco, Helv. Chim. Acta. 4 (1921) 427.
- [19] Rattan A. Antimicrobials in laboratory medicine. 1st ed. New Delhi: Churchill Livingstone (2000) 85.
- [20] Rahul R. Tripathi, Ratnamala P. Sonawane, International Letters of Chemistry, Physics and Astronomy 10(2) (2013) 119-125.
- [21] Mallikarjun S. Yadawe, Shrishila N. Unki, Sangamesh A. Patil, International Letters of Chemistry, Physics and Astronomy 12 (2013) 94-104.
- [22] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
- [23] V. J. Faldu, P. K. Talpara, N. H. Bhuva, P. R. Vachharajani, V. H. Shah, International Letters of Chemistry, Physics and Astronomy 6 (2014) 26-32.
- [24] Piyush B. Vekariya, Jalpa R. Pandya, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 7 (2014) 45-52.
- [25] R. G. Vaghasiya, H. B. Ghodasara, P. R. Vachharajani, V. H. Shah, International Letters of Chemistry, Physics and Astronomy 8 (2014) 30-37.
Uwagi
PL
W wersji online czasopisma błędna numeracja bibliografii
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-5a92083b-7e74-4a77-868e-849ae6e5de3b