Publications by authors named "A Andreotti"

Inhibition of Bruton's tyrosine kinase (BTK) has proven to be highly effective in the treatment of B-cell malignancies such as chronic lymphocytic leukemia (CLL), autoimmune disorders, and multiple sclerosis. Since the approval of the first BTK inhibitor (BTKi), Ibrutinib, several other inhibitors including Acalabrutinib, Zanubrutinib, Tirabrutinib, and Pirtobrutinib have been clinically approved. All are covalent active site inhibitors, with the exception of the reversible active site inhibitor Pirtobrutinib.

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Tattoos have been a ubiquitous phenomenon throughout history. Now, the demand for tattoo removal for aesthetic or practical reasons is growing rapidly. This study outlines the results of field investigations into the chemical and biological removal of tattoo inks (Hexadecachlorinate copper phthalocyanine-CClCuN-CAS no° 1328-53-6).

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Article Synopsis
  • Targeted covalent inhibitors (TCIs) usually rely on specific reactive groups, mainly Michael acceptors, which can vary in stability and selectivity in the body.
  • The study introduces a new group called 2-sulfonylpyrimidine as a promising alternative to the commonly used acrylamide warhead found in Ibrutinib for inhibiting Bruton's tyrosine kinase (BTK).
  • The findings suggest that this new warhead not only performs well in terms of inhibition at low concentrations but also shows better stability and less off-target effects, paving the way for further research on its potential in drug development.
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Purpose: To evaluate the prevalence of deep and superficial dyspareunia in women with diagnosis of endometriosis. Secondly, to assess the temporal relation between deep and superficial dyspareunia in women reporting both symptoms (concomitant dyspareunia) and the impact on quality of life (QoL) and sexual function.

Methods: This is a cross-sectional cohort study that included fertile women with diagnosis of endometriosis.

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The articles in this special issue highlight how modern cellular, biochemical, biophysical and computational techniques are allowing deeper and more detailed studies of allosteric kinase regulation.

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