Synthesis and antiproliferative activity of novel polynuclear heterocyclic compounds derived from 2,3-diaminophenazine

被引:19
作者
Mahran, Asma M. [1 ]
Ragab, Sherif Sh. [1 ]
Hashem, Ahmed I. [2 ]
Ali, Mamdouh M. [3 ]
Nada, Afaf A. [1 ]
机构
[1] Natl Res Ctr, Photochem Dept, Giza, Egypt
[2] Ain Shams Univ, Dept Chem, Fac Sci, Cairo, Egypt
[3] Natl Res Ctr, Dept Biochem, Div Genet Engn & Biotechnol, Giza, Egypt
关键词
Phenazine; Imidazole; Diazepine; Pyrazine; Azo; Antiproliferative; ANTIFUNGAL ACTIVITY; PHENAZINE; STRAIN; REARRANGEMENT; INHIBITORS; SYSTEMS; AGENTS;
D O I
10.1016/j.ejmech.2013.12.007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
2,3-Diaminophenazine 1 was used as a precursor for the preparation of some novel phenazine derivatives such as imidazo[4,5-b]phenazine-2-thione 2, its methylthio 3, ethyl 1-aryl-3H-[1,2,4]triazolo [2,3-a]imidazo[4,5-b]phenazines 8a c, ethyl (2Z)-[3-aminophenazin-2-yl)aminol(phenylhydrazono) ethanoate 9, pyrazino[2,3-b]phenazine derivatives 10, 12, 15-17, [1,4]diazepino[2,3-b]phenazine derivatives 13, 14, 2,3-dibenzoylaminophenazine 18, 1H-Imidazo[4,5-b]phenazine derivatives 20, 23a-c, 24, 25 and 4-[(E)-(3-amino phenazin-2-yl)diazenyl] derivatives 27-29. All compounds were tested as inhibitors of the proliferation of human lung carcinoma and colorectal cancer cell lines through inhibition of Tyrosine Kinases. Most of compounds exert good activity against the two cancer cell lines. Five compounds (1, 2, 3, 25 and 28) were found to possess the same activity as the standard drug Cisplatin. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:568 / 576
页数:9
相关论文
共 36 条
[1]   Izumiphenazines A-C: Isolation and Structure Elucidation of Phenazine Derivatives from Streptomyces sp. IFM 11204 [J].
Abdelfattah, Mohamed S. ;
Kazufumi, Toume ;
Ishibashi, Masami .
JOURNAL OF NATURAL PRODUCTS, 2010, 73 (12) :1999-2002
[2]   On the synthesis of pyrazino[2,3-b] phenazine and 1H-Imidazo[4,5-b]phenazine derivatives [J].
Amer, AM ;
El-Bahnasawi, AA ;
Mahran, MRH ;
Lapib, M .
MONATSHEFTE FUR CHEMIE, 1999, 130 (10) :1217-1225
[3]   Role of tyrosine kinase inhibitors in cancer therapy [J].
Arora, A ;
Scholar, EM .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 315 (03) :971-979
[4]   Peptide inhibitors of protein kinases - discovery, characterisation and use [J].
Bogoyevitch, MA ;
Barr, RK ;
Ketterman, AJ .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2005, 1754 (1-2) :79-99
[5]   AROMATIC NUCLEOPHILIC SUBSTITUTION REACTIONS [J].
BUNNETT, JF ;
ZAHLER, RE .
CHEMICAL REVIEWS, 1951, 49 (02) :273-412
[6]  
BUNNETT JF, 1958, Q REV LONDON, V12, P12
[7]   Potential Chemopreventive Agents Based on the Structure of the Lead Compound 2-Bromo-1-hydroxyphenazine, Isolated from Streptomyces Species, Strain CNS284 [J].
Conda-Sheridan, Martin ;
Marler, Laura ;
Park, Eun-Jung ;
Kondratyuk, Tamara P. ;
Jermihov, Katherine ;
Mesecar, Andrew D. ;
Pezzuto, John M. ;
Asolkar, Ratnakar N. ;
Fenical, William ;
Cushman, Mark .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (24) :8688-8699
[8]   REARRANGEMENT OF ARYL THIOHYDRAZONATES [J].
ELLIOTT, AJ ;
CALLAGHAN, PD ;
GIBSON, MS ;
NEMETH, ST .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1975, 53 (10) :1484-1490
[9]  
Favrel G., 1904, B SOCCHIM FR, V31, P150
[10]   STRUCTURE-ACTIVITY-RELATIONSHIPS OF SELECTED PHENAZINES AGAINST MYCOBACTERIUM-LEPRAE INVITRO [J].
FRANZBLAU, SG ;
OSULLIVAN, JF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (10) :1583-1585