Noviany, Noviany (2016) Synthesis and biological evaluation of 2′-hydroxy-retro-chalcone derivatives as antituberculosis agent. Journal of Chemical and Pharmaceutical Research, 8 (8). pp. 468-474. ISSN 0975-7384

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Abstract

Two new series of 2′-hydroxy-retro-chalcone derivatives have been synthesized and fully characterized by IR, 1H NMR, 13C NMR, and mass spectral data. All of these derivatives were evaluated for their antituberculosis activity against Mycobacterium tuberculosis H37Rv. Eight of the tested compounds inhibited the growth of the mycobacterial strain. Among them, compound (E)-1-[4-(decyloxy)phenyl]-3-(2-hydroxy-5-bromophenyl)prop-2-en-1-one was found to be the most active with MIC value of 27 μM. The results of this study suggest that chalcones are a class of compounds worthy of further investigation as an alternative inexpensive and synthetic therapeutic antituberculosis agent.

Item Type:	Article
Subjects:	Q Science > QD Chemistry
Divisions:	Fakultas Matematika dan Ilmu Pengetahuan Alam (FMIPA) > Prodi Kimia
Depositing User:	Dr Noviany
Date Deposited:	10 Nov 2016 09:20
Last Modified:	10 Nov 2016 09:20
URI:	http://repository.lppm.unila.ac.id/id/eprint/1122

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• Synthesis and biological evaluation of 2′-hydroxy-retro-chalcone derivatives as antituberculosis agent. (deposited 10 Nov 2016 09:20) [Currently Displayed]
  • Synthesis and biological evaluation of 2′-hydroxy-retro-chalcone derivatives as antituberculosis agent. (deposited 22 Nov 2016 01:02)
  • Synthesis and biological evaluation of 2′-hydroxy-retro-chalcone derivatives as antituberculosis agent. (deposited 22 Nov 2016 01:02)

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