ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Nupur Jaiswal, Arvind Kr. Singh

Email(s): adi_arv26@rediffmail.com

DOI: Not Available

Address: Nupur Jaiswal, Arvind Kr. Singh*
Kamla Nehru Institute of Management and Technology (Faculty of Pharmacy), Sultanpur-228001(U.P.) India
*Corresponding Author

Published In:   Volume - 6,      Issue - 2,     Year - 2013


ABSTRACT:
A novel series of 2-Amidino-5-aryl-1,3,4-oxadiazole derivatives (N1-N4) have been synthesized. A mixture of 2-Amino-5-aryl-1,3,4-oxadiazole, powdered anhydrous aluminium chloride and acetonitrile heated in an oil bath keeping the temperature at 150-160°C for 2 hours to synthesize the derivatives (N1-N4). The structures of newly synthesized compounds were established on the basis of FT- IR, 1H NMR and Mass spectroscopic techniques. The newly synthesized compounds were screened for their in vitro antibacterial activity and in vivo anti- inflammatory activity. In vitro anti-bacterial activity was evaluated by Disc Diffusion technique against Ofloxacin used as standard drug. In vivo anti-inflammatory activity was determined by Carageenan Induced Rat Paw Oedema method against Ibuprofen used as standard drug. Compounds N1 and N2 exhibited good antibacterial activity, compound N4 showed moderate antibacterial activity and compound N3 showed poor antibacterial activity. Compound N4 showed good anti-inflammatory activity, compounds N1 and N3 showed moderate anti-inflammatory activity and compound N2 showed poor anti-inflammatory activity.


Cite this article:
Nupur Jaiswal, Arvind Kr. Singh. Synthesis of Some Novel 2,5-Disubstituted 1,3,4-Oxadiazole Derivatives as Potential Antibacterial and Anti-inflammatory activity. Asian J. Research Chem. 6(2): February 2013; Page 111-113.

Cite(Electronic):
Nupur Jaiswal, Arvind Kr. Singh. Synthesis of Some Novel 2,5-Disubstituted 1,3,4-Oxadiazole Derivatives as Potential Antibacterial and Anti-inflammatory activity. Asian J. Research Chem. 6(2): February 2013; Page 111-113.   Available on: https://ajrconline.org/AbstractView.aspx?PID=2013-6-2-4


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