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
  • [21] A facile access to 2-CF3-imidazo[1,2-a]pyridines
    Department of Chemistry, Moscow State University, 119899 Moscow, Russia
    Synthesis, 2002, (10) : 1379 - 1384
  • [22] C2-functionalized imidazo[1,2-a]pyridine: Synthesis and medicinal relevance
    Sharma, Mousmee
    Prasher, Parteek
    SYNTHETIC COMMUNICATIONS, 2022, 52 (11-12) : 1337 - 1356
  • [23] Synthesis of Indeno[1′,2′:4,5]imidazo[1,2-a]pyridin-11-ones and Chromeno[4′,3′:4,5]imidazo[1,2-a]pyridin-6-ones through Palladium-Catalyzed Cascade Reactions of 2-(2-Bromophenyl)imidazo[1,2-a]pyridines
    Zhang, Ju
    Zhang, Xinying
    Fan, Xuesen
    JOURNAL OF ORGANIC CHEMISTRY, 2016, 81 (08) : 3206 - 3213
  • [24] Synthesis, Characterization, and Anticancer Activity of Novel Imidazo[1,2-a]pyridine Linked 1,2,3-Triazole Derivatives
    Srinivas Endoori
    Venkateswara Rao Anna
    Kali Charan Gulipalli
    Srinu Bodige
    Anil Kumar Pommidi
    Sri Ramakrishna Surapureddi
    Nareshvarma Seelam
    Russian Journal of General Chemistry, 2022, 92 : 2082 - 2091
  • [25] Synthesis, Characterization, and Anticancer Activity of Novel Imidazo[1,2-a]pyridine Linked 1,2,3-Triazole Derivatives
    Srinivas Endoori
    Venkateswara Rao anna
    Kali Charan Gulipalli
    Srinu Bodige
    Anil Kumar Pommidi
    Sri Ramakrishna Surapureddi
    Nareshvarma Seelam
    Russian Journal of General Chemistry, 2022, 92 : 1775 - 1784
  • [26] Synthesis and anti-inflammatory activity of imidazo[1,2-a]pyrimidine derivatives
    Jin Pei Zhou~(a
    ChineseChemicalLetters, 2008, (06) : 669 - 672
  • [27] Synthesis, Characterization, and Anticancer Activity of Novel Imidazo[1,2-a]pyridine Linked 1,2,3-Triazole Derivatives
    Endoori, Srinivas
    Anna, Venkateswara Rao
    Gulipalli, Kali Charan
    Bodige, Srinu
    Pommidi, Anil Kumar
    Surapureddi, Sri Ramakrishna
    Seelam, Nareshvarma
    RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2022, 92 (09) : 1775 - 1784
  • [28] Synthesis, Characterization, and Anticancer Activity of Novel Imidazo[1,2-a]pyridine Linked 1,2,3-Triazole Derivatives
    Endoori, Srinivas
    Anna, Venkateswara Rao
    Gulipalli, Kali Charan
    Bodige, Srinu
    Pommidi, Anil Kumar
    Surapureddi, Sri Ramakrishna
    Seelam, Nareshvarma
    RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2022, 92 (10) : 2082 - 2091
  • [29] Synthesis and anti-inflammatory activity of imidazo[1,2-a]pyrimidine derivatives
    Zhou, Jin Pei
    Ding, Yi Wei
    Bin Zhang, Hui
    Xu, Lian
    Dai, Yue
    CHINESE CHEMICAL LETTERS, 2008, 19 (06) : 669 - 672
  • [30] Synthesis and pharmacological activity of amides of 2,3-dihydroimidazo- and 2,3,4,10-tetrahydropyrimido[1,2-a]benzimidazolyln-acetic acids
    V. A. Anisimova
    A. A. Spasov
    V. A. Kosolapov
    I. E. Tolpygin
    E. V. Tibir’kova
    O. A. Salaznikova
    V. A. Kuznetsova
    N. A. Gurova
    K. V. Lenskaya
    D. S. Yakovlev
    D. V. Mal’tsev
    N. A. Kolobrodova
    T. M. Mitina
    O. Yu. Grechko
    Pharmaceutical Chemistry Journal, 2013, 46 : 647 - 652