Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives

被引:102
|
作者
Zarranz, B [1 ]
Jaso, A [1 ]
Aldana, I [1 ]
Monge, A [1 ]
机构
[1] Univ Navarra, Unidad Invest & Desarrollo Medicamentos, Ctr Invest Farmacobiol Aplicada, E-31080 Pamplona, Spain
关键词
D O I
10.1016/S0968-0896(03)00119-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As a continuation of our research and with the aim of obtaining new antituberculosis agents which can improve the current chemotherapeutic antituberculosis treatments, new series of quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives were synthesized and evaluated for in vitro antituberculosis activity against Mycobacterium tuberculosis strain H(37)Rv, using the radiometric BACTEC 460-TB methodology. Active compounds were also screened by serial dilution to assess toxicity to a VERO cell line. The results indicate that some compounds exhibited a good antituberculosis activity and the arylearboxamide analogues 3, 8, and 9 were the most active compounds (EC90/MICI). Also, the cytotoxic effects indicate that these compounds have a good Selectivity Index (SI). (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2149 / 2156
页数:8
相关论文
共 50 条
  • [21] QSAR MODELS FOR QUINOXALINE 1,4-DI-N-OXIDE DERIVATIVES AS ANTITRYPANOSOMAL AGENTS
    Vicente, Esther
    Duchowicz, Pablo R.
    Perez-Silanes, Silvia
    Aldana, Ignacio
    Castro, Eduardo A.
    Cerecetto, Hugo
    Gonzalez, Mercedes
    Monge, Antonio
    DRUGS OF THE FUTURE, 2009, 34 : 151 - 151
  • [22] Synthesis and anticancer activity evaluation of new 2-alkylcarbonyl and 2-benzoyl-3-trifluoromethyl-quinoxaline 1,4-di-N-oxide derivatives
    Zarranz, B
    Jaso, A
    Aldana, I
    Monge, A
    BIOORGANIC & MEDICINAL CHEMISTRY, 2004, 12 (13) : 3711 - 3721
  • [23] REACTION OF QUINOXALINE 1,4-DI-N-OXIDE WITH BENZENESULFONYL CHLORIDE
    ELINA, AS
    JOURNAL OF GENERAL CHEMISTRY USSR, 1964, 34 (08): : 2836 - &
  • [24] Trypanocidal properties, structure-activity relationship and computational studies of quinoxaline 1,4-di-N-oxide derivatives
    Estevez, Yannick
    Quiliano, Miguel
    Burguete, Asuncion
    Cabanillas, Billy
    Zimic, Mirko
    Malaga, Edith
    Verastegui, Manuela
    Perez-Silanes, Silvia
    Aldana, Ignacio
    Monge, Antonio
    Castillo, Denis
    Deharo, Eric
    EXPERIMENTAL PARASITOLOGY, 2011, 127 (04) : 745 - 751
  • [25] Anti-Mycobacterium tuberculosis Activity of Esters of Quinoxaline 1,4-Di-N-Oxide
    Palos, Isidro
    Luna-Herrera, Julieta
    Lara-Ramirez, Edgar E.
    Loera-Piedra, Alejandra
    Fernandez-Ramirez, Emanuel
    Guadalupe Aguilera-Arreola, Ma.
    Paz-Gonzalez, Alma D.
    Monge, Antonio
    Wan, Baojie
    Franzblau, Scott
    Rivera, Gildardo
    MOLECULES, 2018, 23 (06):
  • [26] Synthesis of Quinoxaline 1,4-di-N-Oxide Analogues and Crystal Structure of 2-Carbomethoxy-3-hydroxyquinoxaline-di-N-oxide
    Xu, Yingjun
    Wu, Fanhong
    Yao, Zhiyi
    Zhang, Minmin
    Jiang, Sheng
    MOLECULES, 2011, 16 (08): : 6894 - 6901
  • [27] Synthesis of new 2-acetyl and 2-benzoyl quinoxaline 1,4-di-N-oxide derivatives as anti-Mycobacterium tuberculosis agents
    Jaso, A
    Zarranz, B
    Aldana, I
    Monge, A
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2003, 38 (09) : 791 - 800
  • [28] New 3-methylquinoxaline-2-carboxamide 1,4-di-N-oxide derivatives as anti-Mycobacterium tuberculosis agents
    Ancizu, Saioa
    Moreno, Elsa
    Solano, Beatriz
    Villar, Raquel
    Burguete, Asuncion
    Torres, Enrique
    Perez-Silanes, Silvia
    Aldana, Ignacio
    Monge, Antonio
    BIOORGANIC & MEDICINAL CHEMISTRY, 2010, 18 (07) : 2713 - 2719
  • [29] BENEFICIAL EFFECT OF QUINOXALINE 1,4-DI-N-OXIDE IN RADIATION INJURY IN MICE
    HALEY, TJ
    FLESHER, AM
    VEOMETT, R
    VINCENT, J
    PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1957, 96 (03): : 579 - 582
  • [30] An appraisal on synthetic and pharmaceutical perspectives of quinoxaline 1,4-di-N-oxide scaffold
    Agrawal, Neetu
    Bhardwaj, Aditya
    CHEMICAL BIOLOGY & DRUG DESIGN, 2022, 100 (03) : 346 - 363