Three groups of non-camptothecin compounds with four to five fused rings have been designed and synthesized. Their in vitro anti-proliferative activity has been evaluated with five different cancer cell lines (HCT116, PC3, U87MG, HepG2, SK-OV-3). Compounds B-2 and B-3 showed the most potent cell growth inhibition with IC50 of 169 nM and 325 nM against U87MG cell line correspondingly. (C) 2015 Elsevier Ltd. All rights reserved.National Natural Science Foundation of China (NSFC) [81273370]SCI(E)PubMedARTICLExbmeng@bjmu.edu.cn204693-46962
Topoisomerases are enzymes which alter the topological state of DNA. Mammalian type I and II topoiso...
The natural alkaloid camptothecin is the lead compound of a new class of antitumor agents with a uni...
Two conjugates (1 and 2) of camptothecin (CPT) and 4β-anilino-4′-O-demethylepipodophyllotoxin were p...
A novel series of topoisomerase I (Top I) inhibitors were designed on the basis of camptothecin usin...
Currently, the only topoisomerase I (top1) inhibitors approved by the U.S. Food and Drug Administrat...
In an attempt to synthesize potential anticancer agents acting by inhibition of topoisomerase I (Top...
Cancer is a term used for diseases characterized by out of control cell-growth and rapid creation of...
The preparation and biological evaluation of a novel series of dimeric camptothecin derivatives are ...
The 7-azaindenoisoquinolines are cytotoxic topoisomerase I (Top1) inhibitors. Previously reported re...
DNA topoisomerase I (Top1) is over-expressed in tumour cells and is an important target in cancer ch...
The synthesis of a new hexacyclic system was realized starting from tryptamines and exploiting as a ...
DNA topoisomerase I (Top1) is over-expressed in tumour cells and is an important target in cancer ch...
Topoisomerase type 1 inhibitors represent very important chemotherapeutic agents for various oncolog...
BACKGROUND: Camptothecin (CPT), a pentacyclic alkaloid isolated by Wall et al. in 1958 from the Ch...
Designing multitarget drugs remains a significant challenge in current antitumor drug discovery. Bec...
Topoisomerases are enzymes which alter the topological state of DNA. Mammalian type I and II topoiso...
The natural alkaloid camptothecin is the lead compound of a new class of antitumor agents with a uni...
Two conjugates (1 and 2) of camptothecin (CPT) and 4β-anilino-4′-O-demethylepipodophyllotoxin were p...
A novel series of topoisomerase I (Top I) inhibitors were designed on the basis of camptothecin usin...
Currently, the only topoisomerase I (top1) inhibitors approved by the U.S. Food and Drug Administrat...
In an attempt to synthesize potential anticancer agents acting by inhibition of topoisomerase I (Top...
Cancer is a term used for diseases characterized by out of control cell-growth and rapid creation of...
The preparation and biological evaluation of a novel series of dimeric camptothecin derivatives are ...
The 7-azaindenoisoquinolines are cytotoxic topoisomerase I (Top1) inhibitors. Previously reported re...
DNA topoisomerase I (Top1) is over-expressed in tumour cells and is an important target in cancer ch...
The synthesis of a new hexacyclic system was realized starting from tryptamines and exploiting as a ...
DNA topoisomerase I (Top1) is over-expressed in tumour cells and is an important target in cancer ch...
Topoisomerase type 1 inhibitors represent very important chemotherapeutic agents for various oncolog...
BACKGROUND: Camptothecin (CPT), a pentacyclic alkaloid isolated by Wall et al. in 1958 from the Ch...
Designing multitarget drugs remains a significant challenge in current antitumor drug discovery. Bec...
Topoisomerases are enzymes which alter the topological state of DNA. Mammalian type I and II topoiso...
The natural alkaloid camptothecin is the lead compound of a new class of antitumor agents with a uni...
Two conjugates (1 and 2) of camptothecin (CPT) and 4β-anilino-4′-O-demethylepipodophyllotoxin were p...