Synthesis, Stability, and Antimicrobial Activity of Diiodobromides of 1H,2H,3H,4H-Pyrido-[4,3-d]Pyrimidinium Derivatives

被引:0
作者
Kirsanova, Yu. A. [1 ]
Chernov'yants, M. S. [1 ]
Burykin, I. V. [1 ]
Podoinitsyna, O. A. [2 ]
机构
[1] Southern Fed Univ, Fac Chem, Rostov Na Donu 344090, Russia
[2] Rostov On Don Sci Res Plague Inst, Rostov Na Donu 344002, Russia
关键词
bromides and diiodobromides of 1H,2H,3H,4H-pyrido[4,3-d]pyrimidinium derivatives; stability of iodohalogenides; antimicrobial activity; IODINE;
D O I
10.1007/s11094-015-1303-z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Iodination of chloroform solutions of the bromides of 1H,2H,3H,4H-pyrido[4,3-d]pyrimidinium with a threefold excess of iodine was performed to synthesize the diiodobromides of the corresponding organic cations. The composition and structure of these compounds were confirmed by UV and H-1 NMR spectroscopic and potentiometric titration methods. Values for the stability constant lg beta (3.05 - 4.68) allowed active iodine concentrations at the bactericidal level to be produced in solutions of 1H,2H,3H,4H-pyrido[4,3-d]pyrimidinium diiodobromides. The minimum inhibitory concentrations (MIC) of 1H,2H,3H,4H-pyrido[4,3-d]pyrimidinium diiodobromides against E. coli were 1.0 +/- 0.25 mg/ml.
引用
收藏
页码:455 / 458
页数:4
相关论文
共 12 条
  • [1] [Anonymous], [No title captured], Patent No. [WO 2007105984 A1, 2007105984]
  • [2] Comparison of free and bound iodine and iodide species as a function of the dilution of three commercial povidone-iodine formulations and their microbicidal activity
    Atemnkeng, Magnus A.
    Plaizier-Vercammen, Jacqueline
    Schuermans, Annette
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 317 (02) : 161 - 166
  • [3] Synthesis, spectrophotometry, and X-ray diffraction studies of a new salt:: p-xylylenebis(tetrahydrothiophenium) bis(triiodide)
    Burykin, I. V.
    Chernov'yants, M. S.
    Aleshina, N. V.
    [J]. RUSSIAN CHEMICAL BULLETIN, 2007, 56 (07) : 1390 - 1393
  • [4] Reaction of 1H,2H,3H,4H-pyrido[4,3-d]pyrimidinium bromide derivatives with molecular iodine: Comparative structure and spectroscopic analysis
    Chernov'yants, Margarita S.
    Burykin, Igor V.
    Kostrub, Vladimir V.
    Tsupak, Evgeny B.
    Starikova, Zoya A.
    Kirsanova, Julia A.
    [J]. JOURNAL OF MOLECULAR STRUCTURE, 2012, 1010 : 98 - 103
  • [5] Derffel K. ', 1994, STAT ANAL CHEM
  • [6] Dolinkin AO, 2010, PHARM CHEM J+, V44, P99, DOI 10.1007/s11094-010-0407-8
  • [7] Guiles Joseph W, 2012, Org Med Chem Lett, V2, P5, DOI 10.1186/2191-2858-2-5
  • [8] Solubilization of Hydrophobic Antitumor Drugs (Review)
    Gulyakin, I. D.
    Oborotova, N. A.
    Pechennikov, V. M.
    [J]. PHARMACEUTICAL CHEMISTRY JOURNAL, 2014, 48 (03) : 209 - 213
  • [9] HETZEL BS, 1989, ANNU REV NUTR, V9, P21, DOI 10.1146/annurev.nu.09.070189.000321
  • [10] Synthesis of 1,3-dimethyl-2,4-dioxo-1H,2H,3H,4H-quinazolines and 1,5-dihydro-1,3-dimethyl-5-nitromethyl-2H-pyrano[4,3-d]pyrimidine-2,4(3H)-diones
    Kostrub, Vladimir V.
    Tsupak, Evgeny B.
    Nelyubina, Yulia V.
    [J]. MENDELEEV COMMUNICATIONS, 2009, 19 (04) : 220 - 221