刘新泳, 徐丽君. 抗病毒药物2,5,6-三取代-4(3H)嘧啶酮衍生物的合成及诱导干扰素活性J. 药学学报, 1994, 29(2): 153-157.
引用本文: 刘新泳, 徐丽君. 抗病毒药物2,5,6-三取代-4(3H)嘧啶酮衍生物的合成及诱导干扰素活性J. 药学学报, 1994, 29(2): 153-157.
XY Liu, LJ Xu. SYNTHESIS AND INTERFERON—INDUCING ACTIVITY STUDIES ON THE ANTIVIRAL COMPOUNDS OF 2,5,6-TRISUBSTITUTED-4(3H)PYRIMIDINONE DERIVATIVESJ. Acta Pharmaceutica Sinica, 1994, 29(2): 153-157.
Citation: XY Liu, LJ Xu. SYNTHESIS AND INTERFERON—INDUCING ACTIVITY STUDIES ON THE ANTIVIRAL COMPOUNDS OF 2,5,6-TRISUBSTITUTED-4(3H)PYRIMIDINONE DERIVATIVESJ. Acta Pharmaceutica Sinica, 1994, 29(2): 153-157.

抗病毒药物2,5,6-三取代-4(3H)嘧啶酮衍生物的合成及诱导干扰素活性

SYNTHESIS AND INTERFERON—INDUCING ACTIVITY STUDIES ON THE ANTIVIRAL COMPOUNDS OF 2,5,6-TRISUBSTITUTED-4(3H)PYRIMIDINONE DERIVATIVES

  • Abstract: In order to search for more ideal antiviral drugs,21 substituted pyriiT1idinone derivatives were designed and synthesized,among which 11 were not reported before. The cheinicalstructures were characterized by elemen tal and spectral analysis. The serum interferon - inducing activity was tested in mice. All 2-amino-5-bromo-6-substituted-4-(3H)pyrimidinone compounds were shown to have interferon inducing activity.The corresponding substituted pyrimidine thiones were less active.The new compounds of 6-sulfophenyl derivatives are soluble in、water, but the interferon-inducing activity are not higher than the original compound of ABPP.

     

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