SYNTHESIS AND PHARMACOLOGICAL ACTIVITY OF 3-(2,2,2-TRICHLORO-1-HYDROXYETHYL)IMIDAZO [1,2-a]BENZIMIDAZOLE DIHYDROCHLORIDES

被引:13
|
作者
Anisimova, V. A. [1 ]
Spasov, A. A. [2 ,3 ,4 ]
Kosolapov, V. A. [2 ]
Tolpygin, I. E. [1 ]
Porotikov, V. I.
Kucheryavenko, A. F.
Sysoeva, V. A. [2 ]
Tibir'kova, E. V. [2 ]
El'tsova, L. V. [2 ]
机构
[1] So Fed Univ, Res Inst Phys & Organ Chem, Rostov Na Donu, Russia
[2] Volgograd State Med Univ, Pharmacol Res Inst, Volgograd, Russia
[3] Russian Acad Med Sci, Volgograd Sci Ctr, Volgograd, Russia
[4] Volgograd Reg Adm, Volgograd, Russia
关键词
synthesis; imidazo[1,2-a]benzimidazoles; trichloroethanols; spasmolytic action; antiaggregant activity; radioprotective properties; antiarrhythmic activity; DERIVATIVES;
D O I
10.1007/s11094-009-0340-x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aseries of 3-(2,2,2-trichloro-1-hydroxyethyl)imidazo[1,2-a]benzimidazole dihydrochlorides have been synthesized and their pharmacological properties have been studied. It is established that the synthesized compounds exhibit weak antioxidant activity. In addition, they possess platelet and erythrocyte antiaggregant properties, show pronounced spasmolytic action, and have low toxicity. Some of them also exhibit antiradiomimetic, hypotensive, and antiarrhythmic properties.
引用
收藏
页码:491 / 494
页数:4
相关论文
共 50 条
  • [1] Synthesis and pharmacological activity of 3-(2,2,2-trichloro-1-hydroxyethyl)imidazo [1, 2-a]benzimidazole dihydrochlorides
    V. A. Anisimova
    A. A. Spasov
    V. A. Kosolapov
    I. E. Tolpygin
    V. I. Porotikov
    A. F. Kucheryavenko
    V. A. Sysoeva
    E. V. Tibirˈkova
    L. V. Elˈtsova
    Pharmaceutical Chemistry Journal, 2009, 43 : 491 - 494
  • [2] N-(2,2,2-TRICHLORO-1-HYDROXYETHYL)ARENESULFONAMIDES AND N-(2,2,2-TRICHLORO-1-HYDROXYETHYL)ETHOXYCARBOXIDE IN THE REACTION WITH CHLOROSULFONYLISOCYANATE
    BRYUZGIN, AA
    LEVKOVSKAYA, GG
    MIRSKOVA, AN
    ZHURNAL ORGANICHESKOI KHIMII, 1994, 30 (01): : 63 - 65
  • [3] Synthesis of N-(2,2,2-trichloro-1-hydroxyethyl)aldimines and their derivatives
    Firsova, Yu. N.
    Engel, S. R.
    Lozinskaya, N. A.
    Sosonyuk, S. E.
    Proskurnina, M. V.
    Zefirov, N. S.
    RUSSIAN CHEMICAL BULLETIN, 2015, 64 (01) : 76 - 82
  • [4] Synthesis of N-(2,2,2-trichloro-1-hydroxyethyl)aldimines and their derivatives
    Yu. N. Firsova
    S. R. Engel
    N. A. Lozinskaya
    S. E. Sosonyuk
    M. V. Proskurnina
    N. S. Zefirov
    Russian Chemical Bulletin, 2015, 64 : 76 - 82
  • [5] SYNTHESES OF RADIOACTIVELY LABELED COMPOUNDS .69. SYNTHESIS OF 1-(3,4-DICHLOROPHENYL)-3-(2,2,2-TRICHLORO-1-HYDROXYETHYL)UREA[2-C-14] AND 1-(4-BROMO-PHENYL)-3-(2,2,2-TRICHLORO-1-HYDROXYETHYL)UREA[2-C-14]
    GOTTSTEIN, D
    GROSS, D
    GROSS, M
    KLEPEL, M
    ZEITSCHRIFT FUR CHEMIE, 1990, 30 (09): : 322 - 322
  • [6] Synthesis and pharmacological activity of aminoketones and aminoalcohols of the imidazo[1,2-a]benzimidazole series
    Anisimova V.A.
    Avdyunina N.I.
    Spasov A.A.
    Barchan I.A.
    Pharmaceutical Chemistry Journal, 2002, 36 (7) : 377 - 381
  • [7] Synthesis and pharmacological activity of 2- and 3-(aminomethyl)imidazo[1, 2-a]benzimidazoles
    Anisimova V.A.
    Spasov A.A.
    Kovalev Yu.G.
    Kovalev S.G.
    Dudchenko G.P.
    Pharmaceutical Chemistry Journal, 2004, 38 (10) : 535 - 539
  • [8] Crystal structure of N-(2,2,2-trichloro-1-hydroxyethyl)formamide
    Mariyatra, Mahimaidoss Baby
    Stoeckli-Evans, Helen
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2015, 71 : 1501 - +
  • [9] SYNTHESIS OF 2,3-EPOXYPROPYL ESTERS OF (2,2,2-TRICHLORO-1-HYDROXYETHYL)PHOSPHONIC ACID
    MOLODYKH, ZV
    BARABANO.VI
    JOURNAL OF GENERAL CHEMISTRY USSR, 1969, 39 (10): : 2309 - &
  • [10] Synthesis and Pharmacological Activity of 2,9-Disubstituted Imidazo[1,2-a]Benzimidazole Phenyl- and Alkylthiocarbamides
    V. A. Anisimova
    O. N. Zhukovskaya
    A. A. Spasov
    V. A. Kuznetsova
    V. A. Kosolapov
    D. S. Yakovlev
    O. A. Solov’eva
    D. V. Sorotskii
    A. A. Brigadirova
    E. S. Vorob’ev
    Pharmaceutical Chemistry Journal, 2016, 49 : 653 - 656