Please use this identifier to cite or link to this item: http://dl.umsu.ac.ir/handle/Hannan/23294
Title: Synthesis and evaluation of small libraries of triazolylmethoxy chalcones, flavanones and 2-aminopyrimidines as inhibitors of mycobacterial FAS-II and PknG
Authors: Anand, Namrata;Singh, Priyanka;Sharma, Anindra;Tiwari, Sameer;Singh, Vandana;Singh, D K;Srivastava, K K;Singh, B N;Tripathi, R P
subject: Triazolylmethoxy chalcones;2-Aminopyrimidines;Triazolylmethoxy flavanones;Mycobacterium tuberculosis;FAS-II;PknG
Year: 2012
Description: A synthetic strategy to access small libraries of triazolylmethoxy chalcones 4{1-20}, triazolylmethoxy flavanones 5{1-10} and triazolylmethoxy aminopyrimidines 6{1-17} from a common substrate 4-propargyloxy-2-hydroxy acetophenone using a set of different reactions has been developed. The chalcones and flavanones were screened against mycobacterial FAS-II pathway using a recombinant mycobacterial strain, against which the most potent compound showed ~88% inhibition in bacterial growth and substantially induction of reporter gene activity at 100 µM concentration. The triazolylmethoxy aminopyrimdines were screened against PknG of Mycobaceterium tuberculosis displaying moderate to good activity (23-53% inhibition at 100 µM), comparable to the action of a standard inhibitor.
URI: http://hdl.handle.net/123456789/1033
Standard no: Bioorganic & Medicinal Chemistry 2012, 20 (17), 5150–5163
Appears in Collections:Medicinal and Process Chemistry

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