Nome Químico: 5-Nitro-3-(trifluoromethyl)pyridin-2(1H)-one
Sorrisos: FC(F)(C1=CC([N](=O)=O)=CNC1=O)F
Inchi: InChI=1S/C7H2F3N3O2/c8-7(9,10)5-1-4(13(14)15)3-12-6(5)2-11/h1,3H
Structure-Activity Relationship for Thiohydantoin Androgen Receptor Antagonists for Castration-Resistant Prostate Cancer (CRPC)
Michael E. Jung,*,† Samedy Ouk,† Dongwon Yoo,† Charles L. Sawyers,‡,§ Charlie Chen,‡ Chris Tran,‡ and John Wongvipat
J. Med. Chem. 2010, 53, 2779–2796
Review of Synthetic Routes and Crystalline Forms of the Antiandrogen Oncology Drugs Enzalutamide, Apalutamide, and Darolutamide
David L. Hughes*
Org. Process Res. Dev. 2020, 24, 3, 347–362
Discovery of deshydroxy bicalutamide derivatives as androgen receptor antagonists
S. Kandil, K.Y. Lee, L. Davies, S.A. Rizzo, D.A. Dart, A.D. Westwell, Discovery of deshydroxy bicalutamide derivatives as androgen receptor antagonists, European Journal of Medicinal Chemistry (2019)
European Journal of Medicinal Chemistry Volume 167, 1 April 2019, Pages 49-60