610-50-4Relevant articles and documents
Direct formation of fullerene monolayers using [4+2] Diels-Alder cycloaddition
Ray, Debdas,Belin, Colette,Hui, Fei,Fabre, Bruno,Hapiot, Philippe,Bassani, Dario M.
, p. 2547 - 2549 (2011)
The formation of covalent C60 monolayers through [4+2] Diels-Alder cycloaddition between C60 and anthracene monolayers grafted onto a silicon oxide surface was investigated by ellipsometry, fluorescence and by atomic force microscopy.
Preparation method and application of anthryl hydrogen bond molecular folding material
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, (2019/11/20)
The invention provides a preparation method of an anthryl hydrogen bond molecular folding material and an application of the material in fluorescence recognition, and in particular relates to synthesis and assembly of an anthryl hydrogen bond compound and
Synthesis of Naphthyl-, Quinolin- and Anthracenyl Analogues of Clofibric Acid as PPARα Agonists
Giampietro, Letizia,Ammazzalorso, Alessandra,Bruno, Isabella,Carradori, Simone,De Filippis, Barbara,Fantacuzzi, Marialuigia,Giancristofaro, Antonella,Maccallini, Cristina,Amoroso, Rosa
, p. 467 - 471 (2016/03/12)
PPARα is a ligand activated transcription factor belonging to the nuclear receptor subfamily, involved in fatty acid metabolism in tissues with high oxidative rates such as muscle, heart and liver. PPARα activation is important in steatosis, inflammation and fibrosis in preclinical models of non-alcoholic fatty liver disease identifying a new potential therapeutic area. In this work, three series of clofibric acid analogues conjugated with naphthyl, quinolin, chloroquinolin and anthracenyl scaffolds were synthesized. In an effort to obtain new compounds active as PPARα agonists, these molecules were evaluated for PPARα transactivation activity. Naphthyl and quinolin derivatives showed a good activation of PPARα; noteworthy, optically active naphthyl derivatives activated PPARα better than corresponding parent compound.