ChemMedChem p. 69 - 82 (2015)
Update date:2022-08-11
Topics:
Di Fruscia, Paolo
Zacharioudakis, Emmanouil
Liu, Chang
Moniot, Sébastien
Laohasinnarong, Sasiwan
Khongkow, Mattaka
Harrison, Ian F.
Koltsida, Konstantina
Reynolds, Christopher R.
Schmidtkunz, Karin
Jung, Manfred
Chapman, Kathryn L.
Steegborn, Clemens
Dexter, David T.
Sternberg, Michael J.E.
Lam, Eric W.-F.
Fuchter, Matthew J.
Sirtuins, NAD+-dependent histone deacetylases (HDACs), have recently emerged as potential therapeutic targets for the treatment of a variety of diseases. The discovery of potent and iso-form-selective inhibitors of this enzyme family should pro
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