919488-27-0Relevant articles and documents
Discovery of 7α-substituted dihydrotestosterones as androgen receptor pure antagonists and their structure-activity relationships
Tachibana, Kazutaka,Imaoka, Ikuhiro,Yoshino, Hitoshi,Emura, Takashi,Kodama, Hirohumi,Furuta, Yoshiyuki,Kato, Nobuaki,Nakamura, Mitsuaki,Ohta, Masateru,Taniguchi, Kenji,Ishikura, Nobuyuki,Nagamuta, Masahiro,Onuma, Etsuro,Sato, Haruhiko
, p. 174 - 185 (2007)
A series of 7α-substituted dihydrotestosterone derivatives were synthesized and evaluated for androgen receptor (AR) pure antagonistic activity. From reporter gene assay (RGA), the compound with a side chain containing N-n-butyl-N-methyl amide (19a) showed pure antagonistic activity (IC50 = 340 nM, FI5 > 10,000 nM), whereas known AR antagonists showed partial agonistic activities. The optimization of 19a led to compound 23 (CH4892280), which showed more potent pure antagonistic activity (IC50 = 190 nM, FI5 > 10,000 nM). The SARs of tested compounds suggested that the length of the side chain and the substituents on the amide nitrogen are important for pure antagonistic activities.
