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1.
Nano Lett ; 14(4): 1695-700, 2014.
Article in English | MEDLINE | ID: mdl-24611682

ABSTRACT

A novel method for mapping the charge density spatial distribution in organic field-effect transistors based on the electromodulation of the photoluminescence is demonstrated. In field-effect transistors exciton quenching is dominated by exciton-charge carrier interaction so that it can be used to map the charge distribution in different operating conditions. From a quantitative analysis of the photoluminescence quenching, the thickness of the charge carrier accumulation layer is derived. The injection of minority charge carriers in unipolar conditions is unexpectedly evidenced, which is not displayed by the electrical characteristics.

2.
Eur J Med Chem ; 66: 258-68, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23811088

ABSTRACT

A novel class of low molecular weight ligands of αvß3 and α5ß1 integrins, that possess a dehydro-ß-amino acid as conformationally constrained core, linked to the pharmacophoric moieties mimicking the RGD recognition sequence, have been synthesized through a very simple protocol. Cell adhesion assays and integrin-mediated signaling activation experiments suggested a good affinity of these compounds toward both integrin receptors. Moreover, further elongation with two glycine units allowed to obtain an excellent dual inhibitor. Structural models for αvß3 integrin-ligand binding confirmed that the dehydro-ß-amino derivatives are able to act as an electrostatic clamp by establishing several stabilizing interactions with the receptor.


Subject(s)
Drug Design , Integrin alpha5beta1/metabolism , Integrin alphaVbeta3/metabolism , Peptidomimetics/chemistry , Peptidomimetics/pharmacology , Cell Adhesion/drug effects , Extracellular Signal-Regulated MAP Kinases/metabolism , Fibronectins/metabolism , Humans , Inhibitory Concentration 50 , Integrin alpha5beta1/chemistry , Integrin alphaVbeta3/chemistry , Intracellular Space/drug effects , Intracellular Space/metabolism , K562 Cells , Molecular Docking Simulation , Oligopeptides/chemistry , Peptidomimetics/chemical synthesis , Peptidomimetics/metabolism , Phosphorylation/drug effects , Protein Structure, Tertiary , Signal Transduction/drug effects
3.
Chem Commun (Camb) ; 47(43): 11840-2, 2011 Nov 21.
Article in English | MEDLINE | ID: mdl-21892450

ABSTRACT

The design, synthesis and structure-property investigation of a new thienopyrrolyl dione substituted oligothiophene material showing reduced band gap energy, low lying LUMO energy level and ambipolar semiconducting behaviour is described.

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