New antitumor compounds from Carya cathayensis

2012 ◽  
Vol 22 (5) ◽  
pp. 1895-1898 ◽  
Author(s):  
Wei Wu ◽  
Xiu-Li Bi ◽  
Jia-Qing Cao ◽  
Kai-Qing Zhang ◽  
Yu-Qing Zhao
Keyword(s):  
Antitumor Compounds ◽  
Carya Cathayensis

ChemInform Abstract: New Antitumor Compounds from Carya cathayensis.

ChemInform ◽  
2012 ◽  
Vol 43 (29) ◽  
pp. no-no
Author(s):  
Wei Wu ◽  
Xiu-Li Bi ◽  
Jia-Qing Cao ◽  
Kai-Qing Zhang ◽  
Yu-Qing Zhao
Keyword(s):  
Antitumor Compounds ◽  
Carya Cathayensis

Application of a Validated QSTR Model for Repurposing COX-2 Inhibitor Coumarin Derivatives as Potential Antitumor Agents

2019 ◽  
Vol 19 (13) ◽  
pp. 1121-1128 ◽  
Author(s):  
Gulcin Tugcu ◽  
Hande Sipahi ◽  
Ahmet Aydin
Keyword(s):  
Antitumor Activity ◽  
Drug Development ◽  
Linear Model ◽  
Cell Lines ◽  
Cyclooxygenase 2 ◽  
Large Set ◽  
Coumarin Derivatives ◽  
Antitumor Compounds ◽  
Cyclooxygenase 2 Inhibitors ◽  
Potential Antitumor

Background: The discovery of novel potent molecules for both cancer prevention and treatment has been continuing over the past decade. In recent years, identification of new, potent, and safe anticancer agents through drug repurposing has been regarded as an expeditious alternative to traditional drug development. The cyclooxygenase-2 is known to be over-expressed in several types of human cancer. For this reason cyclooxygenase-2 inhibition may be useful tool for cancer chemotherapy. Objective: The first aim of the study was to develop a validated linear model to predict antitumor activity. Subsequently, applicability of the model for repurposing these cyclooxygenase-2 inhibitors as antitumor compounds to abridge drug development process. Method: We performed a quantitative structure-toxicity relationship (QSTR) study on a set of coumarin derivatives using a large set of molecular descriptors. A linear model predicting growth inhibition on leukemia CCRF cell lines was developed and consequently validated internally and externally. Accordingly, the model was applied on a set of 143 cyclooxygenase-2 inhibitor coumarin derivatives to explore their antitumor activity. Results: The results indicated that the developed QSAR model would be useful for estimating inhibitory activity of coumarin derivatives on leukemia cell lines. Electronegativity was found to be a prominent property of the molecules in describing antitumor activity. The applicability domain of the developed model highlighted the potential antitumor compounds. Conclusion: The promising results revealed that applied integrated in silico approach for repurposing by combining both the biological activity similarity and the molecular similarity via the computational method could be efficiently used to screen potential antitumor compounds among cyclooxygenase-2 inhibitors.

scholarly journals Peppers: A “Hot” Natural Source for Antitumor Compounds

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1521
Author(s):  
Micael Rodrigues Cunha ◽  
Maurício Temotheo Tavares ◽  
Thais Batista Fernandes ◽  
Roberto Parise-Filho
Keyword(s):  
Cell Death ◽  
Cellular Responses ◽  
Biological Applications ◽  
Traditional Use ◽  
Cytotoxic Effects ◽  
Antiproliferative Effects ◽  
Naturally Occurring ◽  
Antitumor Compounds ◽  
Tumorigenic Cells ◽  
Ancient Civilizations

Piper, Capsicum, and Pimenta are the main genera of peppers consumed worldwide. The traditional use of peppers by either ancient civilizations or modern societies has raised interest in their biological applications, including cytotoxic and antiproliferative effects. Cellular responses upon treatment with isolated pepper-derived compounds involve mechanisms of cell death, especially through proapoptotic stimuli in tumorigenic cells. In this review, we highlight naturally occurring secondary metabolites of peppers with cytotoxic effects on cancer cell lines. Available mechanisms of cell death, as well as the development of analogues, are also discussed.

Generation and characterization of nanobubbles in ionic liquid for a green extraction of polyphenols from Carya cathayensis Sarg

2021 ◽  
pp. 130932
Author(s):  
Fatima-ezzahra Ettoumi ◽  
Ruyuan Zhang ◽  
Tarun Belwal ◽  
Miral Javed ◽  
Yanqun Xu ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Green Extraction ◽  
Carya Cathayensis ◽  
Carya Cathayensis Sarg

Antitumor compounds from ipomoea cairica (L.) sweet cell cultures

1996 ◽  
Vol 88 ◽  
pp. 104 ◽  
Author(s):  
Csilla Pàska ◽  
Maria Carrara ◽  
Gabriella Innocenti ◽  
Lorenzo Cima ◽  
Miklòs Làszlò
Keyword(s):  
Cell Cultures ◽  
Antitumor Compounds

scholarly journals The intercalation of imidazoacridinones into DNA induces conformational changes in their side chain.

2000 ◽  
Vol 47 (1) ◽  
pp. 65-78 ◽  
Author(s):  
J Mazerski ◽  
K Muchewicz
Keyword(s):  
Conformational Changes ◽  
Ring System ◽  
Van Der Waals Interactions ◽  
Side Chain ◽  
Intercalation Complex ◽  
Highly Active ◽  
Antitumor Compounds ◽  
Chemical Constitution ◽  
Modelling Techniques ◽  
Dynamics Simulations

Imidazoacridinones (IAs) are a new group of highly active antitumor compounds. The intercalation of the IA molecule into DNA is the preliminary step in the mode of action of these compounds. There are no experimental data about the structure of an intercalation complex formed by imidazoacridinones. Therefore the design of new potentially better compounds of this group should employ the molecular modelling techniques. The results of molecular dynamics simulations performed for four IA analogues are presented. Each of the compounds was studied in two systems: i) in water, and ii) in the intercalation complex with dodecamer duplex d(GCGCGCGCGCGC)2. Significant differences in the conformation of the side chain in the two environments were observed for all studied IAs. These changes were induced by electrostatic as well as van der Waals interactions between the intercalator and DNA. Moreover, the results showed that the geometry of the intercalation complex depends on: i) the chemical constitution of the side chain, and ii) the substituent in position 8 of the ring system.

scholarly journals Steroidal Tetraoxanes - New Class of Antitumor Compounds

1999 ◽  
Author(s):  
Bogdan Solaja ◽  
Dejan Opsenica ◽  
Gabriela Pocsfalvi ◽  
Zorica Juranic
Keyword(s):  
New Class ◽  
Antitumor Compounds
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