| Literature DB >> 14572865 |
Karel Waisser1, Milan Perina, Jirí Kunes, Vera Klimesová, Jarmila Kaustová.
Abstract
A series of derivatives of 3-benzyl-2H-benzoxazine-2,4(3H)-dione substituted in positions 6, 7 or 8 on the benzoxazine, and in positions 3 or 4 on the benzyl moiety was synthesized. The compounds were evaluated for in vitro antimycobacterial activity against Mycobacterium avium and two strains of Mycobacterium kansasii. The disadvantage of the compounds is in their low solubility in water. The antimycobacterial activity of N-benzylsalicylamides correlates with that of 3-benzyl-2H-1,3-benzoxazin-2,4(3H)-diones and depends on the partition coefficients and electronic indexes.Entities:
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Year: 2003 PMID: 14572865 DOI: 10.1016/j.farmac.2003.07.004
Source DB: PubMed Journal: Farmaco ISSN: 0014-827X