AN
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Hydroxyl Ketone-Based Histone Deacetylase Inhibitors To Gain Insight into Class I HDAC Selectivity versus That of HDAC6 | ACS Omega | 2017 | 397 | 296 | |||
| Prediction of retention time in reversed-phase liquid chromatography as a tool for steroid identification | Analytica chimica acta | 2016 | 624 | 1 | |||
| Synthesis of a selective HDAC6 inhibitor active in neuroblasts | Bioorganic & medicinal chemistry letters | 2016 | 392 | 0 | |||
| Cross metathesis with hydroxamate and benzamide BOC-protected alkenes to access HDAC inhibitors and their biological evaluation highlighted intrinsic activity of BOC-protected dihydroxamates | Bioorganic & medicinal chemistry letters | 2016 | 520 | 0 | |||
| Biphenyl-4-yl-acrylohydroxamic acids: Identification of a novel indolyl-substituted HDAC inhibitor with antitumor activity | European journal of medicinal chemistry | 2016 | 457 | 1 | |||
| Investigation on the ZBG-functionality of phenyl-4-yl-acrylohydroxamic acid derivatives as histone deacetylase inhibitors | Bioorganic & medicinal chemistry letters | 2015 | 516 | 0 | |||
| Computational Studies on Sirtuins from Trypanosoma cruzi: Structures, Conformations and Interactions with Phytochemicals | PLoS neglected tropical diseases | 2014 | 651 | 276 | |||
| Aurones as histone deacetylase inhibitors: identification of key features | Bioorganic & medicinal chemistry letters | 2014 | 523 | 2 | |||
| HDAC6 as a target for neurodegenerative diseases: what makes it different from the other HDACs? | Molecular neurodegeneration | 2013 | 678 | 398 | |||
| Unsymmetrical binding modes of HOPNO inhibitor of tyrosinase: From model complexes to the enzyme | Chemistry | 2013 | 876 | 1 | |||
| Role of N-Glycosylation sites and CXC motifs in trafficking of Medicago truncatula Nod factor perception protein to plasma membrane | The Journal of biological chemistry | 2012 | 539 | 0 |
