Abstract:
:1-((Substituted)methyl)quinoxaline-2,3(1H,4H)-dione (2a-e) and 1-((substituted)acryloyl)quinoxaline-2,3(1H,4H)-dione (4a-c) were synthesized from quinoxaline-2,3(1H,4H)-dione 1 and evaluated for their antimicrobial activities. Results of the antitubercular screening against Mycobacterium tuberculosis H(37)Rv showed that the compounds 2b,3, and 4a were the most effective, with minimum inhibitory concentrations of 8.012, 8.561, and 8.928microg/ml, respectively. All the compounds exhibited significant antibacterial and considerable antifungal activities.
journal_name
Bioorg Med Chem Lettjournal_title
Bioorganic & medicinal chemistry lettersauthors
Ramalingam P,Ganapaty S,Rao ChBdoi
10.1016/j.bmcl.2009.10.026subject
Has Abstractpub_date
2010-01-01 00:00:00pages
406-8issue
1eissn
0960-894Xissn
1464-3405pii
S0960-894X(09)01427-9journal_volume
20pub_type
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