Ramamurthy, B and Bhatt, MV (1989) Synthesis and antitubercular activity of N-(2-naphthyl)glycine hydrazide analogs. In: Journal of Medicinal Chemistry, 32 (11). pp. 2421-2426.
![]() |
PDF
jm00131a002.pdf Restricted to Registered users only Download (854kB) | Request a copy |
Abstract
N-(2-Naphthyl)glycine hydrazide analogues were synthesized and tested for possible in vitro antitubercular activity. N-( 2-Naphthy1)alanine hydrazide (3), N-methyl-N-(2-naphthy1)glycine hydrazide (51, N-(6-methoxy-2-naphthyl)glycine hydrazide (7), and 3-(2-naphthylamino)butyric acid hydrazide (23) showed potent inhibitory action against Mycobacterium tuberculosis $H_{37}R_v$ in Youman's medium at concentrations ranging from 0.5 to 10.0 $\mu$g/mL. These compounds showed significant inhibitory action against isonicotinic acid hydrazide and streptomycin-resistant strains of M. tuberculosis. N-(6-Quinolyl)glycine hydrazide (18) and 3-(2-quinolylamino)butpic acid hydrazide (24), which are bioisosteres of compounds 1 and 23, showed loss of antitubercular activity at low concentrations.
Item Type: | Journal Article |
---|---|
Publication: | Journal of Medicinal Chemistry |
Publisher: | Bentham Science Publishers |
Additional Information: | Copyright of this article belongs to Bentham Science Publishers |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry Division of Biological Sciences > Microbiology & Cell Biology |
Date Deposited: | 23 Feb 2008 |
Last Modified: | 19 Sep 2010 04:42 |
URI: | http://eprints.iisc.ac.in/id/eprint/12869 |
Actions (login required)
![]() |
View Item |