Synthesis and properties of several Betti bases as potential drugs

被引:0
作者
Georgieva, N. V. [1 ]
Yaneva, Z. L. [1 ]
Simova, S. D. [2 ]
Nikolova, G. D. [3 ]
机构
[1] Trakia Univ, Fac Vet Med, Dept Pharmacol Anim Physiol & Physiol Chem, Chem Unit, Students Campus, Stara Zagora 6000, Bulgaria
[2] Bulgarian Acad Sci, Ctr Phytochem, Inst Organ Chem, Acad G Bonchev St,Bl 9, BU-1113 Sofia, Bulgaria
[3] Trakia Univ, Fac Med, Dept Med Chem & Biochem, Armejska Str 11, Stara Zagora 6000, Bulgaria
来源
BULGARIAN CHEMICAL COMMUNICATIONS | 2017年 / 49卷
关键词
Betti bases; 8-quinolinol; UV-VIS spectroscopy; EPR spectroscopy; HPLC; DERIVATIVES; 8-QUINOLINOL; INHIBITORS; EFFICIENT; DESIGN;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The aim of the present study was to synthesize several Betti bases by a modified Betti reaction, to develop analytical methods for the quantitative determination and testing the microbiological and antioxidant activities. For the modification of the Betti reaction we used primary heterocyclic amine, aromatic aldehydes, 8-quinolinol and halogeno-substituted aromatic aldehydes. Betti bases were obtained at yield 80-98% and characterized by elemental analysis and NMR spectra. The applied analytical methods for quantitative determination of the studied Betti bases offered short analysis time, high precision, high linearity and satisfactory limit of detection ( LOD) and limit of quantification ( LOQ) values. The microbiological activity of studied Betti bases was tested against 23 test strains pathogenic microorganisms ( different gram positive and gram negative). The microbiological screening proved their selective microbiological activity. According to the EPR study, the Betti bases possess radical structure and are likely to exhibit antioxidant activity. We assume that the potential of the presented Betti bases as a pharmacological compound is promising.
引用
收藏
页码:201 / 208
页数:8
相关论文
共 35 条
  • [1] Design and synthesis of 8-hydroxyquinoline-based radioprotective agents
    Ariyasu, Shinya
    Sawa, Akiko
    Morita, Akinori
    Hanaya, Kengo
    Hoshi, Misato
    Takahashi, Ippei
    Wang, Bing
    Aoki, Shin
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2014, 22 (15) : 3891 - 3905
  • [2] SYNTHESIS OF SOME 5-AZO(4'-SUBSTITUTED BENZENE-SULPHAMOYL)-8-HYDROXYQUINOLINES WITH ANTIDOTAL AND ANTIBACTERIAL ACTIVITIES
    AWAD, IMA
    ALY, AAM
    ABDELALIM, AM
    ABDELAAL, RA
    AHMED, SH
    [J]. JOURNAL OF INORGANIC BIOCHEMISTRY, 1988, 33 (02) : 77 - 89
  • [3] Betti M., 1944, ORG SYNTH COLL, V1, P381
  • [4] SUPEROXIDE AND HYDROGEN-PEROXIDE IN RELATION TO MAMMALIAN-CELL PROLIFERATION
    BURDON, RH
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (04) : 775 - 794
  • [5] The Betti base: the awakening of a sleeping beauty
    Cardellicchio, Cosimo
    Capozzi, Maria Annunziata M.
    Naso, Francesco
    [J]. TETRAHEDRON-ASYMMETRY, 2010, 21 (05) : 507 - 517
  • [6] OXYRADICALS AND CANCER
    CERUTTI, PA
    [J]. LANCET, 1994, 344 (8926) : 862 - 863
  • [7] Total Synthesis of (-)-Cocaine and (-)-Ferruginine
    Cheng, Guolin
    Wang, Xinyan
    Zhu, Rui
    Shao, Changwei
    Xu, Jimin
    Hu, Yuefei
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2011, 76 (08) : 2694 - 2700
  • [8] Chopde N. N., 2014, INT J PHARM PHARM SC, V5, P541
  • [9] Enantiopure α-imino glyoxylate: a versatile substrate for the spontaneous asymmetric synthesis of unnatural hydroxyaryl glycinates
    Cimarelli, Cristina
    Fratoni, Davide
    Mazzanti, Andrea
    Palmieri, Gianni
    [J]. TETRAHEDRON-ASYMMETRY, 2011, 22 (05) : 591 - 596
  • [10] Errico J. P., 2011, Patent, Patent No. [WO2011/85126, 201185126]