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- Repurposing human Aurora kinase inhibitors as leads for anti-protozoan drug discovery. Gautam Patel, Norma E. Roncal, Patricia J. Lee, Susan E. Leed, Jessey Erath, Ana Rodriguez, Richard J. Sciotti, Michael P. Pollastri
, Med. Chem. Commun.
, 2014
, 5
, 655
- Kinome chemoproteomics characterization of pyrrolo[3,4-c]pyrazoles as potent and selective inhibitors of glycogen synthase kinase 3. Martin Golkowski, Gayani K. Perera, Venkata Narayana Vidadala, Kayode K. Ojo, Wesley C. Van Voorhis, Dustin J. Maly, Shao-En Ong
, Mol. Omics
, 2018
, 14
, 26
- Native roles of Baeyer–Villiger monooxygenases in the microbial metabolism of natural compounds. Carmien Tolmie, Martha S. Smit, Diederik J. Opperman
, Nat. Prod. Rep.
, 2019
, 36
, 326
- NIS/CHP-mediated reaction of isocyanides with hydrazones: access to aminopyrazoles. Tong-Hao Zhu, Tian-Qi Wei, Shun-Yi Wang, Shun-Jun Ji
, Org. Chem. Front.
, 2015
, 2
, 259
- Drug repositioning by structure-based virtual screening. Dik-Lung Ma, Daniel Shiu-Hin Chan, Chung-Hang Leung
, Chem. Soc. Rev.
, 2013
, 42
, 2130