2014Unpublished venueRequires access

Synthesis and Antibacterial Activity of Novel Quinoxaline-5-Carboxamide Derivatives

Keesari Srinivas, Teneti Raghavender Reddy, Vurimidi Himabindu, Ghanta Mahesh Reddy, Nerusu Jagan Mohan

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Abstract

Quinoxaline-based molecules have been disclosed as the antibacterial and antiprotozoal properties. The present paper describes the synthesis and antibacterial activity of sixteen new quinoxaline-5-carboxamide derivatives (5a-5p) from commercially available methyl 2, 3-diamino benzoate as staring material. The quinoxaline carboxamides (5a-5p) have been screened against four bacterial strains such Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pyogenes. In general, it is observed that within the quinoxaline-5-carboxamides 5a–5p, compounds incorporated with Fluoro substituent phenyl groups, cyclic and aliphatic chain exhibited excellent antibacterial activity while the remaining compounds displayed moderate antibacterial activity.

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What this paper is about

Quinoxaline-based molecules have been disclosed as the antibacterial and antiprotozoal properties. The present paper describes the synthesis and antibacterial activity of sixteen new quinoxaline-5-carboxamide derivatives (5a-5p) from commercially available methyl 2, 3-diamino benzoate as staring material. The quinoxaline carboxamides (5a-5p) have been screened against four bacterial strains such Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pyogenes. In general, it is observed that within the quinoxaline-5-carboxamides 5a–5p, compounds incorporated with Fluoro substituent phenyl groups, cyclic and aliphatic chain exhibited excellent antibacterial activity while the remaining compounds displayed moderate antibacterial activity.

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Available abstract

Quinoxaline-based molecules have been disclosed as the antibacterial and antiprotozoal properties. The present paper describes the synthesis and antibacterial activity of sixteen new quinoxaline-5-carboxamide derivatives (5a-5p) from commercially available methyl 2, 3-diamino benzoate as staring material. The quinoxaline carboxamides (5a-5p) have been screened against four bacterial strains such Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pyogenes. In general, it is observed that within the quinoxaline-5-carboxamides 5a–5p, compounds incorporated with Fluoro substituent phenyl groups, cyclic and aliphatic chain exhibited excellent antibacterial activity while the remaining compounds displayed moderate antibacterial activity.

Key concepts: Quinoxaline, Antibacterial activity, Carboxamide, Chemistry, Substituent, Antiprotozoal, Staphylococcus aureus, Escherichia coli

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