PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 7528148-12 1994 Both 15-OH TZP-4238 and cyproterone acetate also reduced the androgen receptor and DHT contents to 50%. Cyproterone Acetate 24-43 androgen receptor Rattus norvegicus 61-78 8331696-7 1993 In the competitive binding assay, procymidone showed a significant but lower binding affinity comparing to that of cyproterone acetate, the steroidal androgen receptor antagonist, for the androgen receptor in both rats and mice under the condition that unlabeled dihydrotestosterone (DHT) effectively inhibited the binding of [3H]-DHT to the androgen receptor in both species. Cyproterone Acetate 115-134 androgen receptor Rattus norvegicus 188-205 10935541-7 2000 Similarly, antiandrogenic ligands, cyproterone acetate and casodex, were also capable of translocating the cytoplasmic AR into the nucleus albeit at a slower rate than the androgen 5alpha-dihydrotestosterone (DHT). Cyproterone Acetate 35-54 androgen receptor Rattus norvegicus 119-121 10935541-8 2000 All AR ligands with transactivation potential, including the mixed agonist/antagonist cyproterone acetate, caused translocation of the GFP-AR into a subnuclear compartment indicated by its punctate intranuclear distribution. Cyproterone Acetate 86-105 androgen receptor Rattus norvegicus 4-6 3758193-3 1986 We determined the short-term and long-term competition of cyproterone acetate and chlormadinone acetate with [3H]DHT for receptor binding at 0 degrees C and showed, that the complexes formed by these antiandrogens with the androgen receptor have equally reduced stabilities compared to the DHT-receptor complex. Cyproterone Acetate 58-77 androgen receptor Rattus norvegicus 223-240 2930988-0 1985 Interactions of an anti-androgen (cyproterone acetate) with the androgen receptor system and its biological action in the rat ventral prostate. Cyproterone Acetate 34-53 androgen receptor Rattus norvegicus 64-81 6227511-0 1983 Cyproterone acetate prevents translocation of the androgen receptor in the rat prostate. Cyproterone Acetate 0-19 androgen receptor Rattus norvegicus 50-67 6227511-1 1983 The translocation of the androgen receptor in prostatic tissue has been studied under the influence of different ligands (testosterone, methyltrienolone and cyproterone acetate) in vivo and in vitro. Cyproterone Acetate 157-176 androgen receptor Rattus norvegicus 25-42 7263637-4 1981 This affinity to the androgen receptor is 1,000-, 500-, 120-, and 40-fold lower than that of 5 alpha-dihydrotestosterone, testosterone, spironolactone, and cyproterone acetate, respectively, and 7-fold higher than that of cimetidine. Cyproterone Acetate 156-175 androgen receptor Rattus norvegicus 21-38 6453438-10 1981 These data suggest that estradiol-17 beta may have a more potent antiandrogenic effect on the epididymis than cyproterone acetate due to inhibition of 5 alpha reduction of testosterone as well as binding to the androgen receptor. Cyproterone Acetate 110-129 androgen receptor Rattus norvegicus 211-228 465307-2 1979 When the androgen-receptor blocking-agent cyproterone acetate was administered together with the testosterone, the subsequent vasopressin treatment did not cause renal cortical necrosis. Cyproterone Acetate 42-61 androgen receptor Rattus norvegicus 9-26 18346198-9 2008 The DHT-mediated increase in NEP expression and decrease in Abeta levels were (i) not observed in rat pheochromocytoma cell 12 lacking AR and (ii) blocked in AR-expressing cells by the antagonists, cyproterone acetate and flutamide. Cyproterone Acetate 198-217 androgen receptor Rattus norvegicus 158-160 12215663-9 2002 CPA caused effects consistent with its mixed AR antagonist/progesterone receptor agonist activity: it decreased ASG weights, caused hormonal alterations (increased T and E2; decreased FSH), and caused spermatid retention. Cyproterone Acetate 0-3 androgen receptor Rattus norvegicus 45-47