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1 ed through structure-guided modifications of androgen receptor antagonists.
2 ovides strong rationale for developing novel androgen receptor antagonists.
3 ues were prepared and evaluated as potential androgen receptor antagonists against two human prostate
4 NP1 was absent with co-administration of the androgen receptor antagonist bicalutamide and in androge
5                    Conversely, flutamide, an androgen receptor antagonist, did not affect androgen st
6 ed males and those receiving the competitive androgen receptor antagonist flutamide had significantly
7 fically, we bilaterally implanted the potent androgen receptor antagonist flutamide in two key brain
8                                 Finally, the androgen receptor antagonist flutamide inhibited the inc
9  were reversed by in vivo treatment with the androgen receptor antagonist flutamide, suggesting that
10     Moreover, prenatal administration of the androgen receptor antagonist, flutamide, equalizes devel
11 T4 in vivo and in vitro were reversed by the androgen receptor antagonist, flutamide, indicating that
12 caused by hCG treatment was prevented by the androgen receptor antagonist, flutamide.
13 F-0998425, (-)- 6a] is a novel, nonsteroidal androgen receptor antagonist for sebum control and treat
14 nowledge, DIM is the first example of a pure androgen receptor antagonist from plants.
15                  Treatment with estrogen and androgen receptor antagonists had opposite effects on Le
16 ains androgen-receptor dependent, and potent androgen-receptor antagonists induce tumour regression i
17 ific antigen and objective responses with an androgen receptor antagonist (MDV3100).
18 at mediate a switch in function of selective androgen receptor antagonists/modulators (SARMs) from re
19 osterone was repressed by co-exposure to the androgen receptor antagonist nilutamide supporting a pot
20                         A novel nonsteroidal androgen receptor antagonist, (R)-4-(1-benzyl-4,4-dimeth
21                                              Androgen receptor antagonists showed agonistic activity
22                                MDV3100 is an androgen-receptor antagonist that blocks androgens from
23                                  Several new androgen receptor antagonists were synthesized and found

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