Antimycobacterial activity of novel hydrazide-hydrazone derivatives with 2H-chromene and coumarin scaffold

被引:82
|
作者
Angelova, Violina T. [1 ]
Valcheva, Violeta [2 ]
Vassilev, Nikolay G. [3 ]
Buyukliev, Rosen [1 ]
Momekov, Georgi [4 ]
Dimitrov, Ivan [1 ]
Saso, Luciano [5 ]
Djukic, Mirjana [6 ]
Shivachev, Boris [7 ]
机构
[1] Med Univ Sofia, Dept Chem, Fac Pharm, 2 Dunav St, Sofia 1000, Bulgaria
[2] Bulgarian Acad Sci, Inst Microbiol, 26 Acad G Bonchev St, BU-1113 Sofia, Bulgaria
[3] Bulgarian Acad Sci, Ctr Phytochem, Inst Organ Chem, Lab Nucl Magnet Resonance, 9 Acad G Bonchev St, BU-1113 Sofia, Bulgaria
[4] Med Univ Sofia, Lab Expt Chemotherapy, Dept Pharmacol Pharmacotherapy & Toxicol, Fac Pharm, 2 Dunav St, Sofia 1000, Bulgaria
[5] Sapienza Univ, Dept Physiol & Pharmacol Vittorio Erspamer, Ple Aldo Moro 5, I-00185 Rome, Italy
[6] Univ Belgrade, Dept Toxicol, Fac Pharm, 450 Vojvode Stepe St, Belgrade 11221, Serbia
[7] Bulgarian Acad Sci, Inst Mineral & Crystallog, 107 Acad G Bonchev St, Sofia 1113, Bulgaria
关键词
Antitmycobacterial activity; 2H-Chromene; Coumarin; Cytotoxicity; Hydrazide-hydrazone; ANTITUBERCULAR ACTIVITY; ISONIAZID DERIVATIVES; TUBERCULOSIS; DESIGN; AGENTS; TB; MDR;
D O I
10.1016/j.bmcl.2016.11.071
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study reports the synthesis of new 2H-chromene or coumarin based acylhydrazones, which were evaluated for their in vitro antimycobacterial activity against reference strain Mycobacterium tuberculosis H37Rv and compared to the first-line antituberculosis drugs, isoniazid (INH) and ethambutol (EMB). The most active compounds 7m (MIC 0.13 mu M), 7o (MIC 0.15 mu M) and 7k (MIC 0.17 mu M) demonstrated antimycobacterial activity at submicromolar concentration level and remarkably minimal associated cytotoxicity in the human embryonic kidney cell line HEK-293T. Structure-activity relationship for this class of compounds has been established. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:223 / 227
页数:5
相关论文
共 50 条
  • [11] Investigation of Antimicrobial Activity of Some Ethylparaben Hydrazide-Hydrazone Derivatives
    Ince, Ufuk
    Han, M. Ihsan
    TURKISH JOURNAL OF PHARMACEUTICAL SCIENCES, 2023, 20 (01) : 35 - 38
  • [12] Design, synthesis, antioxidant and anticholinesterase activities of novel isonicotinic hydrazide-hydrazone derivatives
    Aslanhan, Ozlem
    Kalay, Erbay
    Tokali, Feyzi Sinan
    Can, Zehra
    Sahin, Engin
    JOURNAL OF MOLECULAR STRUCTURE, 2023, 1279
  • [13] NOVEL SYNTHESIS OF PYRAN-3-HYDRAZIDE DERIVATIVES AND THEIR USES TO THE SYNTHESIS HYDRAZIDE-HYDRAZONE, PYRAZOLE AND THIAZOLE DERIVATIVES WITH ANTICANCER ACTIVITIES
    Samir, Eman M.
    Mohareb, Rafat M.
    BULLETIN OF THE CHEMICAL SOCIETY OF ETHIOPIA, 2021, 35 (03) : 573 - 586
  • [14] Cytotoxicity of Novel Hydrazide-hydrazone Derivatives towards Tumor and Normal Cell Lines
    Zaki, Mayssoune Y.
    EGYPTIAN JOURNAL OF CHEMISTRY, 2013, 56 (01): : 25 - 34
  • [15] Reaction of pregnenolone with cyanoacetylhydrazine: Novel synthesis of hydrazide-hydrazone, pyrazole, pyridine, thiazole, thiophene derivatives and their cytotoxicity evaluations
    Mohareb, Rafat M.
    Al-Omran, Fatima
    STEROIDS, 2012, 77 (14) : 1551 - 1559
  • [16] Synthesis of Some New Hydrazide-Hydrazone and 2-Pyridone Derivatives of Potential Biological Interest
    Al-Mola, Istabrick M.
    Al-Sabawi, Ammar H.
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY, 2023, 33 (04) : 413 - 416
  • [17] Synthesis, antitumor activity and mechanism of action of novel 1,3-thiazole derivatives containing hydrazide-hydrazone and carboxamide moiety
    He, Haifeng
    Wang, Xiaoyan
    Shi, Liqiao
    Yin, Wenyan
    Yang, Ziwen
    He, Hongwu
    Liang, Ying
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 26 (14) : 3263 - 3270
  • [18] Antiproliferative and antioxidative effects of novel hydrazone derivatives bearing coumarin and chromene moiety
    Angelova, Violina T.
    Vassilev, Nikolay G.
    Nikolova-Mladenova, Boryana
    Vitas, Jasmina
    Malbasa, Radomir
    Momekov, Georgi
    Djukic, Mirjana
    Saso, Luciano
    MEDICINAL CHEMISTRY RESEARCH, 2016, 25 (09) : 2082 - 2092
  • [19] Synthesis and larvicidal and adult topical activity of some hydrazide-hydrazone derivatives against Aedes aegypti
    Akdag, Kadriye
    Kocyigit-Kaymakcioglu, Bedia
    Tabanca, Nurhayat
    Ali, Abbas
    Estep, Alden
    Becnel, James J.
    Khan, Ikhlas A.
    MARMARA PHARMACEUTICAL JOURNAL, 2014, 18 (03) : 120 - 125
  • [20] Synthesis, antiproliferative and apoptosis induction potential activities of novel bis(indolyl) hydrazide-hydrazone derivatives
    Sreenivasulu, Reddymasu
    Reddy, Kotthireddy Thirumal
    Sujitha, Pombala
    Kumar, C. Ganesh
    Raju, Rudraraju Ramesh
    BIOORGANIC & MEDICINAL CHEMISTRY, 2019, 27 (06) : 1043 - 1055