Results
1 -
10 of
11Bradner et al..
Chemical Phylogenetics of Histone Deacetylases, Nature Chemical Biology, 2010 Zhang Xin, Lv Peng-Cheng, Li Dong-Dong, Zhang Wei-Ming, Zhu Hai-Liang.
Navigating into the chemical space between MGCD0103 and SAHA: novel histone deacetylase inhibitors as a promising lead, Med. Chem. Commun., 2015 J. Liu, T. Wang, X. Wang, L. Luo, J. Guo, Y. Peng, et al..
6 Becher et al.
Thermal profiling reveals phenylalanine hydroxylase as an off-target of panobinostat.
Nature Chemical Biology, doi: 10.1038/nchembio.2185, published online 26 September 2016, Nature Chemical Biology Y. Depetter, S. Geurs, F. Vanden Bussche, R. De Vreese, J. Franceus, T. Desmet, et al..
6 Guan Longfei, Yang Hongbin, Cai Yingchun, Sun Lixia, Di Peiwen, Li Weihua, Liu Guixia, Tang Yun.
ADMET-score – a comprehensive scoring function for evaluation of chemical drug-likeness, MedChemComm, 2019 Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D..
Panobinostat, Pharmaceutical Substances [Online], Thieme: Stuttgart, (2016). Pierre, Romain; Gaigne, Fr?d?ric; El-Bazbouz, Ghizlane; Mouis, Gr?goire; Ouvry, Gilles; Tomas, Loic; Harris, Craig S..
Identification of 1,5,7-Triazabicyclododecene and Polystyrene-Supported Superbases as Efficient Hydroxylaminolysis Agents of Sterically Hindered and Epimerizable Esters, Pierre, Romain; Gaigne, Fr?d?ric; El-Bazbouz, Ghizlane; Mouis, Gr?goire; Ouvry, Gilles; Tomas, Loic; Harris, Craig S., Synlett 2018, 29, 1102-1106