In the current medical era, spirooxindole motif stands out as a privileged heterospirocyclic scaffold that represents the core for a wide range of bioactive naturally isolated products (such as Strychnofoline and spirotryprostatins A and B) and synthetic compounds. Interestingly, no much attention has been paid to develop spirooxindole derivatives with dual antioxidant and anticancer activities. In this context, a series of spirooxindoles 6a-p was examined for their anticancer effect towards HepG2 hepatocellular carcinoma and PC-3 prostate cancer cell lines. Spirooxindole 6a was found to be an efficient anti-proliferative agent towards both HepG2 and PC-3 cells (IC50 = 6.9 and 11.8 µM, respectively). Afterwards, spirooxindole 6a was assesse...
The Authors thank the Unite de Nutition Humaine UMR 1019 INRA-UdA - Equipe ECREIN (France) and the U...
A highly stereoselective, one-pot, multicomponent method has been developed to synthesize pyrrolizid...
Spirobibenzopyrans are an unexplored class of therapeutics. We report the anticancer activity of nov...
Triple-negative breast cancer (TNBC) is a highly aggressive malignancy with limited treatment option...
A series of novel spirooxindole-O-naphthoquinone-tetrazolo[1,5-a]pyrimidine hybrids were designed, s...
<div><p>Anticancer role of andrographolide is well documented. To find novel potent derivatives with...
A new series of spirooxindoles based on ethylene derivatives having furan aryl moiety are reported. ...
The tumor resistance to p53 activators posed a clinical challenge. Combination studies disclosed tha...
Owing to the downsides of existing anticancer drugs, it is necessary to find more effective and sele...
Here, we report the design of new analogues of spirooxoindolepyrrolidine nucleus as modulators of p5...
Here, we report the design of new analogues of spirooxoindolepyrrolidine nucleus as modulators of p5...
Aim: Inhibition of P53-mdm2 interaction will lead to cancer cell apoptosis. This strategy was achiev...
Cancer is still one of the deadliest diseases worldwide despite the deep understanding of its etiolo...
This paper describes the rational development of a series of novel spiroindoline derivatives endowed...
The Authors thank the Unite de Nutition Humaine UMR 1019 INRA-UdA - Equipe ECREIN (France) and the U...
A highly stereoselective, one-pot, multicomponent method has been developed to synthesize pyrrolizid...
Spirobibenzopyrans are an unexplored class of therapeutics. We report the anticancer activity of nov...
Triple-negative breast cancer (TNBC) is a highly aggressive malignancy with limited treatment option...
A series of novel spirooxindole-O-naphthoquinone-tetrazolo[1,5-a]pyrimidine hybrids were designed, s...
<div><p>Anticancer role of andrographolide is well documented. To find novel potent derivatives with...
A new series of spirooxindoles based on ethylene derivatives having furan aryl moiety are reported. ...
The tumor resistance to p53 activators posed a clinical challenge. Combination studies disclosed tha...
Owing to the downsides of existing anticancer drugs, it is necessary to find more effective and sele...
Here, we report the design of new analogues of spirooxoindolepyrrolidine nucleus as modulators of p5...
Here, we report the design of new analogues of spirooxoindolepyrrolidine nucleus as modulators of p5...
Aim: Inhibition of P53-mdm2 interaction will lead to cancer cell apoptosis. This strategy was achiev...
Cancer is still one of the deadliest diseases worldwide despite the deep understanding of its etiolo...
This paper describes the rational development of a series of novel spiroindoline derivatives endowed...
The Authors thank the Unite de Nutition Humaine UMR 1019 INRA-UdA - Equipe ECREIN (France) and the U...
A highly stereoselective, one-pot, multicomponent method has been developed to synthesize pyrrolizid...
Spirobibenzopyrans are an unexplored class of therapeutics. We report the anticancer activity of nov...