928-46-1Relevant articles and documents
Self-assembled monolayers of a tetrathiafulvalene-based redox-switchable ligand
Trippe, Gaelle,Ocafrain, Maitena,Besbes, Mohamed,Monroche, Vincent,Lyskawa, Joel,Le Derf, Franck,Salle, Marc,Becher, Jan,Colonna, Barbara,Echegoyen, Luis
, p. 1320 - 1323 (2002)
A straightforward synthesis of new thiol derivatives incorporating the tetrathiafulvalene (TTF) moiety is presented. These electroactive systems form highly stable self-assembled monolayers (SAMs) on gold electrodes. The electrode obtained by SAM formation from a thiol derivative whose structure associates the redox-active TTF unit and a crown-ether ligating part, allows the voltammetric recognition of barium.
MONOAMINE OXIDASE INHIBITORS AND METHODS FOR TREATMENT AND DIAGNOSIS OF PROSTATE CANCER
-
Paragraph 120, (2013/03/26)
A mechanism of monoamine oxidases (MAOs) driven epithelium-to-mesenchymal transition (EMT) is disclosed. Also disclosed are methods for treating cancer by inhibiting or suppressing MAOs in cancer cells. Novel MAOs inhibitors, such as small molecules, siRN
Electrochemical cleavage of azo linkage for site-selective immobilization and cell patterning
Jung, Hyun Joo,Min, Hyegeun,Yu, Hyunung,Lee, Tae Geol,Chung, Taek Dong
supporting information; experimental part, p. 3863 - 3865 (2010/07/13)
A new molecular structure of azobenzene, which can be reduced to the corresponding anilines at a low reduction potential for the site-selective immobilization of biomolecules, is proposed. Redox-active species, enzymes, peptides, and cultured hippocampal neurons can be effectively immobilized on the electrochemically activated surface.
