Synthesis and Pharmacological Studies of Unprecedented Fused Pyridazino[3′,4′:5,6][1,2,4]triazino[3,4-b][1,3,4]thiadiazine Derivatives

被引:6
作者
Ali, Rania S. [1 ,2 ]
Saad, Hosam A. [1 ,3 ]
机构
[1] Taif Univ, Dept Chem, Fac Sci, At Taif 21974, Saudi Arabia
[2] Helwan Univ, Fac Ind Educ, Dept Basic Sci, Cairo 11795, Egypt
[3] Zagazig Univ, Dept Chem, Fac Sci, Zagazig 44511, Egypt
来源
MOLECULES | 2018年 / 23卷 / 05期
关键词
pyridazino[3 ',4 ':5,6][1,2,4]triazino[4,3-b][1,2,4,5]tetrazine; antitumor activity; biological applications; cyclization reactions; NITROGEN SYSTEMS BEARING; 1,2,4-TRIAZINE MOIETY; ANTICANCER DRUGS; ANTI-HIV; CRYSTAL-STRUCTURE; CYTOTOXIC AGENTS; IDENTIFICATION; ANTITUMOR; THIOPHENES;
D O I
10.3390/molecules23051024
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
A novel fused system with three or four fused ringspyridazino[3,4:5,6][1,2,4]triazino[4,3-b][1,2,4,5]tetrazine and pyridazino[3,4:5,6][1,2,4]triazino[3,4-b]pyrimido[4,5-e][1,3,4]thiadiazine was obtained from the starting materials 4(6H)-amino-3-hydrazino-7-(2-thienyl)pyridazino[3,4-e][1,2,4]-triazine 2 and 9-amino-3-(2-thienyl)-2H,8H-pyridazino[3,4:5,6][1,2,4]triazino[3,4-b][1,3,4]thiadiazine-8-carbonitrile 12. Each of the starting compounds was subjected to a number of cyclization reactions to obtain a series of new heterocyclic fused systems, 3-10 and 13-23, via bifunctional reagents. Some of the synthesized compounds were screened against three cell lines including HepG2, HCT-116 and MCF-7 to discover their anticancer activity. The synthesized compounds were characterized depending on their elemental analyses and spectral data.
引用
收藏
页数:17
相关论文
共 34 条
[1]  
Abdel-Rahman RM, 1999, PHARMAZIE, V54, P347
[2]  
Abdel-Rahman RM, 1999, PHARMAZIE, V54, P667
[3]   Thieno[2,3-b]indole-Based Small Push-Pull Chromophores: Synthesis, Structure, and Electronic Properties [J].
Baert, Francois ;
Cabanetos, Clement ;
Allain, Magali ;
Silvestre, Virginie ;
Leriche, Philippe ;
Blanchard, Philippe .
ORGANIC LETTERS, 2016, 18 (07) :1582-1585
[4]   Synthesis of Schiff bases by aromatic amine condensation with 3,3′-bithiophenes-2,2′ and 4,4′-dicarbaldehydes [J].
Benachenhou, Fatiha ;
Mesli, Abderrezzak ;
Guilard, Roger .
ARABIAN JOURNAL OF CHEMISTRY, 2013, 6 (03) :313-317
[5]   Synthesis of new pyrazolo[5,1-c][1,2,4] benzotriazines, pyrazolo[5,1-c]pyrido[4,3-e][1,2,4] triazines and their open analogues as cytotoxic agents in normoxic and hypoxic conditions [J].
Ciciani, Giovanna ;
Coronnello, Marcella ;
Guerrini, Gabriella ;
Selleri, Silvia ;
Cantore, Miriam ;
Failli, Paola ;
Mini, Enrico ;
Costanzo, Annarella .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (21) :9409-9419
[6]   Cytotoxic activity of 3-nitropyrazolo[5,1-c][12,4]benzotriazine derivatives:: a new series of anti-proliferative agents [J].
Coronnello, M ;
Ciciani, G ;
Mini, E ;
Guerrini, G ;
Caciagli, B ;
Selleri, S ;
Costanzo, A ;
Mazzei, T .
ANTI-CANCER DRUGS, 2005, 16 (06) :645-651
[7]  
Deep Aakash, 2016, Central Nervous System Agents in Medicinal Chemistry, V16, P158, DOI 10.2174/1871524916666160204114424
[8]   Synthesis and antimicrobial screening of 1,3,4-oxadiazole and clubbed thiophene derivatives [J].
Desai, N. C. ;
Dodiya, Amit M. ;
Rajpara, Kiran M. ;
Rupala, Yogesh M. .
JOURNAL OF SAUDI CHEMICAL SOCIETY, 2014, 18 (03) :255-261
[9]   Synthesis and structure elucidation of novel fused 1,2,4-triazine derivatives as potent inhibitors targeting CYP1A1 activity [J].
El Massry, Abdel Moneim ;
Asal, Ahmed Mosaad ;
Khattab, Sherine Nabil ;
Haiba, Nesreen Saied ;
Awney, Hala A. ;
Helmy, Mohamed ;
Langer, Vratislav ;
Amer, Adel .
BIOORGANIC & MEDICINAL CHEMISTRY, 2012, 20 (08) :2624-2637
[10]  
El-Gendy Z, 2001, PHARMAZIE, V56, P376