Artur M. S. Silva
University of Aveiro
976 Papers
4.9K Citations
Artur M. S. Silva is an academic researcher from University of Aveiro. The author has contributed to research in topics: Chemistry & Catalysis. The author has an hindex of 54, co-authored 895 publications. Previous affiliations of Artur M. S. Silva include University of Porto & University of Santiago de Compostela.
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Papers
Chemical Composition of Lipophilic Bark Extracts from Pinus pinaster and Pinus pinea Cultivated in Portugal
Joana L. C. Sousa,Patrícia A. B. Ramos,Carmen S. R. Freire,Artur M. S. Silva,Armando J. D. Silvestre +4 more
TL;DR: In this paper, the chemical composition of lipophilic pine extracts from Pinus pinaster and Pinus pinea was evaluated using gas chromatography-mass spectrometry and Diterpenic resin acids were found to be the main components.
Amyloid-β and tau aggregation dual-inhibitors: A synthetic and structure-activity relationship focused review.
TL;DR: In this paper, a review summarizes the state-of-the-art in the field of dual-target inhibitors of both amyloid-β plaques (Aβ) and tau aggregation simultaneously, including the design and synthetic strategy of the dual target compounds, as well as a brief structure-activity relationships (SAR) analysis.
Two new saponins from Paronychia capitata
Zina Allaoua,Imane Benabdelaziz,Naima Rahmouni,Soumia Bouzidi,Artur M. S. Silva,Mohammed Benkhaled,H. Haba +6 more
TL;DR: In this paper , two triterpene glycosides from the butanol extract of Paronychia capitata (L.) Lam, along with seven known compounds were identified.
New polyhydroxylated flavon-3-ols and 3-hydroxy-2-styrylchromones: synthesis and ROS/RNS scavenging activities
TL;DR: This work allowed the establishment of new structure-activity relationships and brought the knowledge about the selective choice of a structure depending on the targeted reactive species to be brought.
Antitumor Activity of Some Prenylated Xanthones
Raquel A. P. Castanheiro,Artur M. S. Silva,Nair Campos,Maria São José Nascimento,Madalena Pinto +4 more
TL;DR: The structural elucidation of the two new compounds 6,11, as well as an update of data for the already described prenylated derivatives 7,8,10 were accomplished by IR, UV, HRMS and NMR techniques.