Synthesis, Antimicrobial and Pharmacological Evaluation of Thiourea-derivatives of 4H-1,2,4-triazole

被引:17
|
作者
Bielenica, Anna [1 ]
Kedzierska, Ewa [2 ]
Fidecka, Sylwia [2 ]
Maluszynska, Hanna [3 ]
Miroslaw, Barbara [4 ]
Koziol, Anna E. [4 ]
Stefanska, Joanna [5 ]
Madeddu, Silvia [6 ]
Giliberti, Gabriele [6 ]
Sanna, Giuseppina [6 ]
Struga, Marta [7 ]
机构
[1] Med Univ Warsaw, Chair & Dept Biochem, PL-02097 Warsaw, Poland
[2] Med Univ Lublin, Dept Pharmacol & Pharmacodynam, Lublin, Poland
[3] Adam Mickiewicz Univ, Fac Phys, PL-61614 Poznan, Poland
[4] Marie Curie Sklodowska Univ, Fac Chem, PL-20031 Lublin, Poland
[5] Med Univ, Dept Pharmacol Microbiol, PL-02007 Warsaw, Poland
[6] Univ Cagliari, Dept Biomed Sci, I-09042 Monserrato, CA, Italy
[7] Med Univ Warsaw, Fac Pharm, Dept Pharmacogen, PL-02097 Warsaw, Poland
关键词
Antifungal activity; antiviral activity; CNS activity; thiourea; 1,2,4-triazole; X-ray crystallography; 5-HT2B RECEPTOR ANTAGONIST; BIOLOGICAL EVALUATION; PYRAZOLE DERIVATIVES; SEROTONIN RECEPTORS; EFFICIENT SYNTHESIS; FACILE SYNTHESIS; INHIBITORS; AGENTS; POTENT; 1,2,4-TRIAZOLES;
D O I
10.2174/1570180811666141001010044
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A group of 4H-1,2,4-triazole-derived thioureas was efficiently prepared and evaluated for antibacterial, antifungal and antiviral activities. The chemical identity of all derivatives was established on the basis of spectral methods. The molecular structures of 10 and 21 were determined by an X-ray crystallography. Compounds with phenyl (1), 3,4-dichlorophenyl (2) and p-methoxyphenyl (3) substituents were the most promising against fungi species. The derivative 12 has proved to be significantly active against CVB-5. The CNS-activity of five new 4H-1,2,4-triazolo-thiourea derivatives 2, 10, 12, 18 and 21 was investigated. The results proved that activity of all tested thiourea compounds may be connected with the serotonergic system. Derivatives 2, 10, 12, 18 acted as inhibitors of the head twitch responses (HTR). The biological activity of 21 was also linked with the endogenous opioid system. The derivative 18 diminished the spontaneous mobility and 10 reduced the amphetamine-induced activity of laboratory animals.
引用
收藏
页码:263 / 276
页数:14
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