Optimized Synthesis of New Thiosemicarbazide Derivatives with Tuberculostatic Activity

被引:8
|
作者
Popovici, Corina [1 ,2 ]
Pavel, Cristina-Maria [3 ]
Sunel, Valeriu [1 ]
Cheptea, Corina [4 ]
Dimitriu, Dan Gheorghe [3 ]
Dorohoi, Dana Ortansa [3 ]
David, Diana [5 ]
Closca, Valentina [3 ,6 ]
Popa, Marcel [2 ]
机构
[1] Alexandru Ioan Cuza Univ, Fac Chem, 11 Carol Blvd, Iasi 700506, Romania
[2] Gheorghe Sachi Tech Univ, Fac Chem Engn & Environm Protect, Dept Nat & Synthet Polymers, 73 Prof Dimitrie Mangeron Blvd, Iasi 700050, Romania
[3] Alexandru Ioan Cuza Univ, Fac Phys, 11 Carol Blvd, Iasi 700506, Romania
[4] Grigore T Popa Univ Med & Pharm, Dept Biomed Sci, Fac Med Bioengn, 9-13 M Kogalniceanu Str, Iasi 700454, Romania
[5] Univ Warwick, Warwick Med Sch, Coventry CV4 7AL, W Midlands, England
[6] Eudoxiu Hurmuzachi Natl Coll, Dept Sci, 5 Calea Bucovinei Str, Radauti 725400, Romania
关键词
2-mercapto-benzimidazole; sulfonic derivatives; heterocyclic thiosemicarbazides; tuberculostatic activity; ANTIMICROBIAL ACTIVITY; COMPLEXES; 1,2,4-TRIAZOLO;
D O I
10.3390/ijms222212139
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Original results are presented in the field of research that addresses the extension of the reaction of residue of acyl-thiosemicarbazide fixation on the structure of 5-nitrobenzimidazole by a sulphonic group. The aim of the study is the increase of new thiosemicarbazide derivatives' applicative potential in the field of biochemistry, with a wide range of medical applications. The newly obtained compounds were characterized by using elemental analysis and spectral analysis (FT-IR and H-1 NMR). A study regarding the optimization of the chemical reactions was made. The performed in vitro biological tests confirmed the tuberculostatic activity of three newly obtained compounds against Mycobacterium tuberculosis.
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页数:14
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