Synthesis and antiproliferative activity of new 1,5-disubstituted tetrazoles bearing hydrazone moiety

被引:22
|
作者
Kaplancikli, Zafer Asim [1 ]
Yurttas, Leyla [1 ]
Ozdemir, Ahmet [1 ]
Turan-Zitouni, Gulhan [1 ]
Ciftci, Gulsen Akalin [2 ]
Yildirim, Safak Ulusoylar [3 ]
Abu Mohsen, Usama [4 ]
机构
[1] Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-26470 Eskisehir, Turkey
[2] Anadolu Univ, Fac Pharm, Dept Biochem, TR-26470 Eskisehir, Turkey
[3] Anadolu Univ, Fac Pharm, Dept Pharmacol, TR-26470 Eskisehir, Turkey
[4] Al Azhar Univ, Fac Pharm, Dept Pharmaceut Chem, Gaza, Israel
关键词
Tetrazole; Hydrazone; MTT assay; Antiproliferative activity; Caspase-3; BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; DERIVATIVES; APOPTOSIS; CELLS; ANTIBACTERIAL; ANTIFUNGAL; INHIBITORS; AGENTS;
D O I
10.1007/s00044-013-0717-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new class of tetrazole-hydrazone derivatives including chloro-substituted phenyl moiety were synthesized to perform anticancer activity screening. The structural elucidation of the compounds was performed by IR, H-1 NMR, C-13 NMR, MS spectral, and elemental analyses data. Anticancer effect of the compounds was evaluated against A549 and C6 tumor cell lines. MTT, analysis of DNA synthesis and analysis of caspase-3 activation assays were carried out for anticancer activity investigations. Compounds N'-(2-chlorobenzylidene)-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanohydrazide (3d), N'-(2,3-dichlorobenzylidene)-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanohydrazide (3d), and N'-(3,4-dichlorobenzylidene)-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanohydrazide (3e) showed significant anticancer activity. Anticancer screening tests also indicated that compound 3d has potential on C6 tumor cells with apoptotic pathway.
引用
收藏
页码:1067 / 1075
页数:9
相关论文
共 50 条
  • [21] α-ferrocenylalkylation of 1,5-disubstituted tetrazoles and certain transformations of reaction products
    Krasnikova, EM
    Moskalenko, AI
    Kopaeva, NA
    Boev, VI
    RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2003, 73 (09) : 1468 - 1475
  • [22] α-Ferrocenylalkylation of 1,5-Disubstituted Tetrazoles and Certain Transformations of Reaction Products
    E. M. Krasnikova
    A. I. Moskalenko
    N. A. Kopaeva
    V. I. Boev
    Russian Journal of General Chemistry, 2003, 73 : 1468 - 1475
  • [23] Ionic liquid-assisted synthesis of 5-mono- and 1,5-disubstituted tetrazoles
    Epishina, Margarita A.
    Kulikov, Alexander S.
    Ignat'ev, Nikolai V.
    Schulte, Michael
    Makhova, Nina N.
    MENDELEEV COMMUNICATIONS, 2011, 21 (06) : 334 - 336
  • [24] Isocyanide-based four-component synthesis of ferrocenyl 1,5-disubstituted tetrazoles
    Amanpour, Tayebeh
    Mirzaei, Peiman
    Bazgir, Ayoob
    TETRAHEDRON LETTERS, 2012, 53 (11) : 1421 - 1423
  • [25] Facile synthesis of 1,5-disubstituted tetrazoles by reacting a ruthenium acetylide complex with trimethylsilyl azide
    Chang, Chao-Wan
    Cheng, Ming-Chuan
    Lee, Gene-Hsiang
    Peng, Shie-Ming
    DALTON TRANSACTIONS, 2019, 48 (31) : 11732 - 11742
  • [26] A two-step synthesis of 1,5-disubstituted tetrazoles containing a siloxy or sulfonamide group
    Sarvary, Afshin
    Shaabani, Shabnam
    Shaabani, Ahmad
    Ng, SeikWeng
    TETRAHEDRON LETTERS, 2011, 52 (45) : 5930 - 5933
  • [27] Preparation of 1,5-disubstituted tetrazoles under phase-transfer conditions
    Artamonova, TV
    Zhivich, AB
    Dubinskii, MY
    Koldobskii, GI
    SYNTHESIS-STUTTGART, 1996, (12): : 1428 - &
  • [28] Improved conditions for converting sterically hindered amides to 1,5-disubstituted tetrazoles
    Schroeder, Gretchen M.
    Marshall, Sydney
    Wan, Honghe
    Purandare, Ashok V.
    TETRAHEDRON LETTERS, 2010, 51 (10) : 1404 - 1406
  • [29] Synthesis of symmetrical 1,5-disubstituted granatanines
    Vartak, Ashish P.
    Dwoskin, Linda P.
    Crooks, Peter A.
    TETRAHEDRON LETTERS, 2008, 49 (44) : 6330 - 6333
  • [30] A Convenient One-Pot Synthesis of 1,5-Disubstituted Tetrazoles Containing an Amino or a Carboxy Group
    N. T. Pokhodylo
    O. Ya. Shyyka
    M. D. Obushak
    Russian Journal of Organic Chemistry, 2020, 56 : 802 - 812