کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2196107 | 1550891 | 2014 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Preclinical pharmacology of FL442, a novel nonsteroidal androgen receptor modulator Preclinical pharmacology of FL442, a novel nonsteroidal androgen receptor modulator](/preview/png/2196107.png)
• FL442 is selective to AR over other closely related steroid hormone receptors.
• FL442 exhibits equal efficacy to prevent PCa cell proliferation as enzalutamide.
• FL442 maintains antiandrogenic activity with enzalutamide-activated ARF876L.
• FL442 accumulates strongly in the mouse prostate.
• FL442 significantly inhibits LNCaP xenograft tumor growth.
The preclinical profiles of two most potent compounds of our recently published cycloalkane[d]isoxazole pharmacophore-based androgen receptor (AR) modulators, FL442 (4-(3a,4,5,6,7,7a-hexahydro-benzo[d]isoxazol-3-yl)-2-(trifluoromethyl)benzonitrile) and its nitro analog FL425 (3-(4-nitro-3-(trifluoromethyl)phenyl)-3a,4,5,6,7,7a-hexahydrobenzo[d]isoxazole), were explored to evaluate their druggability for the treatment of AR dependent prostate cancer. The studies revealed that both compounds are selective to AR over other closely related steroid hormone receptors and that FL442 exhibits equal inhibition efficiency towards the androgen-responsive LNCaP prostate cancer cell line as the most widely used antiandrogen bicalutamide and the more recently discovered enzalutamide. Notably, FL442 maintains antiandrogenic activity with enzalutamide-activated AR mutant F876L. In contrast to bicalutamide, FL442 does not stimulate the VCaP prostate cancer cells which express elevated levels of the AR. Distribution analyses showed that [14CN]FL442 accumulates strongly in the mouse prostate. In spite of its low plasma concentration obtained by intraperitoneal administration, FL442 significantly inhibited LNCaP xenograft tumor growth. These findings provide a preclinical proof for FL442 as a promising AR targeted candidate for a further optimization.
Journal: Molecular and Cellular Endocrinology - Volume 387, Issues 1–2, 25 April 2014, Pages 8–18