In this study, we examined the cytotoxic effects of seven ent-labdane derivatives 1–7 (0–100 μM) in different human cancer cell lines. Our results showed that compounds 1–3 exhibited significant dose-dependent inhibition on the growth of the three different human cell lines, according to the sulphorhodamine B assay and produced morphological changes consistent with apoptosis, as confirmed by Hoestch 3342 staining analysis. They induced apoptosis in various cancer cell lines, as shown by nuclear condensation and fragmentation and caspase 3 activation. Such induction was associated with the depletion of mitochondrial membrane potential. These activities led to the cleavage of caspases and the trigger of cell death process. Overall, the compou...
Objective: The primary objective of this study was to probe the cytotoxic capacity of the labdane di...
A modern approach in the search for new bioactive molecules is the synthesis of novel chemical entit...
Cancer persists as a global challenge due to the extent to which conventional anticancer therapies p...
© 2021 by the authors.Terpenylquinones are mixed biogenesis primary or secondary metabolites widespr...
The labdane diterpene sclareol has demonstrated significant cytotoxicity against human tumor cell li...
Here, we tested seven 2-acylated-1,4-hydronaphthoquinones for their cytotoxic effects on a panel of ...
Novel cationic dimethylaminopyridine derivatives of pentacyclic triterpenes were previously describe...
Extensive research over the past decades has identified numerous phytochemicals that could represent...
This article describes the preparation of 2-heteroaryl and 2,3-diheteroaryl-1,4-naphthoquinones by a...
We have designed and synthesized three novel compounds, 5-isopropylidiene derivatives of 3-dimethyl-...
AbstractSesquiterpene lactones (SLs) are natural products with a variety of biological activities. P...
In our continuing search to discover bioactive compounds from natural products, we isolated six new ...
International audienceHuman hepatocellular carcinoma (HCC) is the most common type of liver cancer, ...
Thirteen anthraquinone derivatives 5-17 including two 3-(3- alkylaminopropoxy)-9,10-anthraquinone (N...
International audienceSince cancer treatment by radio- and chemotherapy has been linked to safety co...
Objective: The primary objective of this study was to probe the cytotoxic capacity of the labdane di...
A modern approach in the search for new bioactive molecules is the synthesis of novel chemical entit...
Cancer persists as a global challenge due to the extent to which conventional anticancer therapies p...
© 2021 by the authors.Terpenylquinones are mixed biogenesis primary or secondary metabolites widespr...
The labdane diterpene sclareol has demonstrated significant cytotoxicity against human tumor cell li...
Here, we tested seven 2-acylated-1,4-hydronaphthoquinones for their cytotoxic effects on a panel of ...
Novel cationic dimethylaminopyridine derivatives of pentacyclic triterpenes were previously describe...
Extensive research over the past decades has identified numerous phytochemicals that could represent...
This article describes the preparation of 2-heteroaryl and 2,3-diheteroaryl-1,4-naphthoquinones by a...
We have designed and synthesized three novel compounds, 5-isopropylidiene derivatives of 3-dimethyl-...
AbstractSesquiterpene lactones (SLs) are natural products with a variety of biological activities. P...
In our continuing search to discover bioactive compounds from natural products, we isolated six new ...
International audienceHuman hepatocellular carcinoma (HCC) is the most common type of liver cancer, ...
Thirteen anthraquinone derivatives 5-17 including two 3-(3- alkylaminopropoxy)-9,10-anthraquinone (N...
International audienceSince cancer treatment by radio- and chemotherapy has been linked to safety co...
Objective: The primary objective of this study was to probe the cytotoxic capacity of the labdane di...
A modern approach in the search for new bioactive molecules is the synthesis of novel chemical entit...
Cancer persists as a global challenge due to the extent to which conventional anticancer therapies p...