The aim of this study was to investigate the in vitro cellular activity of novel spiroisoxazoline type compounds against normal and cancer cell lines from lung tissue (Hs888Lu), neuron-phenotypic cells (SH-SY5Y), neuroblastoma (SH-SY5Y), human histiocytic lymphoma (U937), lung cancer (A549), and leukaemia (HL-60). Our bioassay program revealed that the spiroisoxazoline type compounds show cytotoxicity only in lymphoma cell lines, which is in contrast with the pyrrolidine precursor of these spiroisoxazoline compounds, where significant cytotoxicity is seen in all normal and cancer cell lines. These data suggest a tumour-specific mechanism of action. In addition these data also show that spiroisoxazoline compounds are non-toxic in the human n...
<div><p>Anticancer role of andrographolide is well documented. To find novel potent derivatives with...
<p>All other compounds prepared in this work were also tested but their activities on these 10 cell ...
A series of novel spirooxindole-O-naphthoquinone-tetrazolo[1,5-a]pyrimidine hybrids were designed, s...
The aim of this study was to investigate the in vitro cellular activity of novel spiroisoxazoline ty...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
Marine-originated spirocyclic bromotyrosines are considered as promising scaffolds for new anticance...
The research aim was to test cytotoxic effects in vitro of seven novel pyrazolothiazolopyrimidine de...
In this study, we evaluated the antiproliferative potential, DNA damage, crystal structures, and doc...
The Authors thank the Unite de Nutition Humaine UMR 1019 INRA-UdA - Equipe ECREIN (France) and the U...
The present study is to investigate the cytotoxicity properties and haematological indices of synthe...
Lung cancer is one of the most diagnosed cancers worldwide and the development of anticancer agents ...
Spirobibenzopyrans are an unexplored class of therapeutics. We report the anticancer activity of nov...
In the current medical era, spirooxindole motif stands out as a privileged heterospirocyclic scaffol...
Cancer is still one of the deadliest diseases worldwide despite the deep understanding of its etiolo...
The association between glioblastoma (GBM) and human cytomegalovirus (HCMV) infection has been the i...
<div><p>Anticancer role of andrographolide is well documented. To find novel potent derivatives with...
<p>All other compounds prepared in this work were also tested but their activities on these 10 cell ...
A series of novel spirooxindole-O-naphthoquinone-tetrazolo[1,5-a]pyrimidine hybrids were designed, s...
The aim of this study was to investigate the in vitro cellular activity of novel spiroisoxazoline ty...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
Marine-originated spirocyclic bromotyrosines are considered as promising scaffolds for new anticance...
The research aim was to test cytotoxic effects in vitro of seven novel pyrazolothiazolopyrimidine de...
In this study, we evaluated the antiproliferative potential, DNA damage, crystal structures, and doc...
The Authors thank the Unite de Nutition Humaine UMR 1019 INRA-UdA - Equipe ECREIN (France) and the U...
The present study is to investigate the cytotoxicity properties and haematological indices of synthe...
Lung cancer is one of the most diagnosed cancers worldwide and the development of anticancer agents ...
Spirobibenzopyrans are an unexplored class of therapeutics. We report the anticancer activity of nov...
In the current medical era, spirooxindole motif stands out as a privileged heterospirocyclic scaffol...
Cancer is still one of the deadliest diseases worldwide despite the deep understanding of its etiolo...
The association between glioblastoma (GBM) and human cytomegalovirus (HCMV) infection has been the i...
<div><p>Anticancer role of andrographolide is well documented. To find novel potent derivatives with...
<p>All other compounds prepared in this work were also tested but their activities on these 10 cell ...
A series of novel spirooxindole-O-naphthoquinone-tetrazolo[1,5-a]pyrimidine hybrids were designed, s...