Literature DB >> 17516578

The oriented development of antituberculotics (Part II): halogenated 3-(4-alkylphenyl)-1,3-benzoxazine-2,4-(3H)-diones.

Karel Waisser1, Josef Matyk, Hana Divisová, Petra Husáková, Jirí Kunes, Vera Klimesová, Karel Palát, Jarmila Kaustová.   

Abstract

Based on our previous studies, 21 new halogenated 3-(4-alkylphenyl)-1,3-benzoxazine-2,4-(3H)-diones were synthesized by the reaction of salicylanilides and methyl-chloroformate. All compounds were screened in vitro against three different strains of mycobacterium, and Free-Wilson method was used to establish structure-activity relationships. 6-Bromo-3-(4-butylphenyl)-1,3-benzoxazine-2,4-(3H)-dione 3b proved to be the most active compound of the series.

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Year:  2007        PMID: 17516578     DOI: 10.1002/ardp.200600002

Source DB:  PubMed          Journal:  Arch Pharm (Weinheim)        ISSN: 0365-6233            Impact factor:   3.751


  1 in total

1.  Synthesis of 3,5-isoxazolidinediones and 1H-2,3-benzoxazine-1,4(3H)-diones from aliphatic oximes and dicarboxylic acid chlorides.

Authors:  Robert A Izydore; Joseph T Jones; Benjamin Mogesa; Ira N Swain; Ronda G Davis-Ward; Dwayne L Daniels; Felicia Frazier Kpakima; Sharnelle T Spaulding-Phifer
Journal:  J Org Chem       Date:  2014-03-21       Impact factor: 4.354

  1 in total

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