Synthesis and biological evaluation of new 1,2-dihydro-4-hydroxy-2-oxo-3-quinolinecarboxamides for treatment of autoimmune disorders:: Structure-activity relationship

被引:141
|
作者
Jönsson, S [1 ]
Andersson, G [1 ]
Fex, T [1 ]
Fristedt, T [1 ]
Hedlund, G [1 ]
Jansson, K [1 ]
Abramo, L [1 ]
Fritzson, I [1 ]
Pekarski, O [1 ]
Runström, A [1 ]
Sandin, H [1 ]
Thuvesson, I [1 ]
Björk, A [1 ]
机构
[1] Active Biotech Res AB, SE-22007 Lund, Sweden
关键词
D O I
10.1021/jm031044w
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Roquinimex-related 3-quinolinecarboxamide derivatives were prepared and evaluated for treatment of autoimmune disorders. The compounds were tested in mice for their inhibitory effects on disease development in the acute experimental autoimmune encephalomyelitis model and selected compounds in the beagle dog for induction of proinflammatory reaction. Structure-activity relationships are discussed. Compound 8c, laquinimod, showed improved potency and superior toxicological profile compared to the lead compound roquinimex (1b, Linomide) and was selected for clinical studies (currently in phase II).
引用
收藏
页码:2075 / 2088
页数:14
相关论文
共 50 条
  • [1] Reaction of isatin-1-acetamides with alkoxides: Synthesis of novel 1,4-dihydro-3-hydroxy-4-oxo-2-quinolinecarboxamides
    Blanco, Maria Mercedes
    Dal Maso, Monica
    Shmidt, Maria Sol
    Perillo, Isabel Amalia
    SYNTHESIS-STUTTGART, 2007, (06): : 829 - 834
  • [2] 4-hydroxy-2-quinolones 165*. 1-R-4-hydroxy-2-oxo-1,2-dihydro-quinoline-3-carbaldehydes and their thiosemicarbazones. Synthesis, structure, and biological properties
    I. V. Ukrainets
    Liu Yangyang
    A. A. Tkach
    O. V. Gorokhova
    A. V. Turov
    Chemistry of Heterocyclic Compounds, 2009, 45 : 705 - 714
  • [3] 4-HYDROXY-2-QUINOLONES 165. 1-R-4-HYDROXY-2-OXO-1,2-DIHYDRO-QUINOLINE-3-CARBALDEHYDES AND THEIR THIOSEMICARBAZONES. SYNTHESIS, STRUCTURE, AND BIOLOGICAL PROPERTIES
    Ukrainets, I. V.
    Liu Yangyang
    Tkach, A. A.
    Gorokhova, O. V.
    Turov, A. V.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2009, 45 (06) : 705 - 714
  • [4] 4-Hydroxy-2-quinolones 171*. Synthesis, isomerism, and antitubercular activity of 1-R-4-hydroxy-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid alkylidenehydrazides
    I. V. Ukrainets
    Liu Yangyang
    A. A. Tkach
    A. V. Turov
    O. S. Golovchenko
    Chemistry of Heterocyclic Compounds, 2009, 45 : 1335 - 1342
  • [5] 4-HYDROXY-2-QUINOLONES 171*. SYNTHESIS, ISOMERISM, AND ANTITUBERCULAR ACTIVITY OF 1-R-4-HYDROXY-2-OXO-1,2-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ALKYLIDENEHYDRAZIDES
    Ukrainets, I. V.
    Liu Yangyang
    Tkach, A. A.
    Turov, A. V.
    Golovchenko, O. S.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2009, 45 (11) : 1335 - 1342
  • [6] 4-Hydroxy-2-quinolones. 221.* Synthesis, structure, and biological activity of 3-(3-(alkylcarbamoyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-1-yl)propanoic acids
    I. V. Ukrainets
    K. V. Andreeva
    O. V. Gorokhova
    V. N. Kravchenko
    Chemistry of Heterocyclic Compounds, 2013, 48 : 1809 - 1816
  • [7] 4-Hydroxy-2-quinolones. 221.* Synthesis, structure, and biological activity of 3-(3-(alkylcarbamoyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-1-yl)propanoic acids
    Ukrainets, I. V.
    Andreeva, K. V.
    Gorokhova, O. V.
    Kravchenko, V. N.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2013, 48 (12) : 1809 - 1816
  • [8] SYNTHESIS, BIOLOGICAL EVALUATION, AND QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP OF "1H-ISOINDOLE-1,3-(2-HYDROXY)-DIONES AS NEW CYTOSTATIC AGENTS
    CHAN, CL
    TOKES, ZA
    LIEN, EJ
    PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH, 1986, 27 : 284 - 284
  • [9] Synthesis, biological evaluation and structure-activity relationship of new GABA uptake inhibitors, derivatives of 4-aminobutanamides
    Kowalczyk, Paula
    Salat, Kinga
    Hoefner, Georg C.
    Mucha, Marta
    Rapacz, Anna
    Podkowa, Adrian
    Filipek, Barbara
    Wanner, Klaus T.
    Kulig, Katarzyna
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 83 : 256 - 273
  • [10] Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-(4,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-ypcarbonyl-amino)alkanamido] alkanoate
    Fathalla, Walid
    Pazdera, Pavel
    ARKIVOC, 2017, : 158 - 173