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Effect of steroids with antiandrogenic properties on androgenic and myotrophic activity of testosterone and some of its derivatives.

作者信息

Ivanenko T I

出版信息

Neurosci Behav Physiol. 1980 May-Jun;10(3):227-31. doi: 10.1007/BF01182216.

DOI:10.1007/BF01182216
PMID:7413078
Abstract
摘要

相似文献

1
Effect of steroids with antiandrogenic properties on androgenic and myotrophic activity of testosterone and some of its derivatives.具有抗雄激素特性的类固醇对睾酮及其某些衍生物的雄激素活性和促肌营养活性的影响。
Neurosci Behav Physiol. 1980 May-Jun;10(3):227-31. doi: 10.1007/BF01182216.
2
[Effect of steroids with anti-androgenic properties on the androgenic and myotrophic activity of testosterone and its various derivatives].[具有抗雄激素特性的类固醇对睾酮及其各种衍生物的雄激素活性和促肌营养活性的影响]
Probl Endokrinol (Mosk). 1978 Jul-Aug;24(4):86-91.
3
Dissociation of anabolic and androgenic properties of steroids by anti-anabolic and anti-androgenic agents in rats.
Endocrinology. 1971 Sep;89(3):894-6. doi: 10.1210/endo-89-3-894.
4
Prodrugs utilizing organosilyl derivation: an investigation of the long-term androgenic and myotrophic activities of silyl derivatives of testosterone.利用有机硅烷基衍生化的前药：睾酮硅烷基衍生物的长期雄激素和促肌营养活性研究。
J Pharm Sci. 1988 Feb;77(2):116-9. doi: 10.1002/jps.2600770205.
5
[Anabolic activity of 9, 10-dehydro-19-nortestosterone derivatives].[9,10-脱氢-19-去甲睾酮衍生物的合成代谢活性]
Probl Endokrinol (Mosk). 1974 Jul-Aug;20(4):83-8.
6
Anti-androgen TSAA-291. VII. On the mechanism of anti-androgenic action of 16 beta-ethyl-17 beta-hydroxy-4-oestren-3-one (TSAA-291).抗雄激素TSAA-291。VII。关于16β-乙基-17β-羟基-4-雌甾烯-3-酮（TSAA-291）抗雄激素作用机制的研究
Acta Endocrinol Suppl (Copenh). 1979;229:100-7.
7
Anti-androgen TSAA-291. I. Anti-androgenic effects of a new steroid TSAA-291 (16 beta-ethyl-17 beta-hydroxy-4-oestren-3-one) and its derivatives.抗雄激素TSAA - 291。I. 新型甾体TSAA - 291（16β - 乙基 - 17β - 羟基 - 4 - 雌甾烯 - 3 - 酮）及其衍生物的抗雄激素作用。
Acta Endocrinol Suppl (Copenh). 1979;229:2-23.
8
5alpha-reduction of norethisterone enhances its binding affinity for androgen receptors but diminishes its androgenic potency.炔诺酮的5α-还原增强了其对雄激素受体的结合亲和力，但降低了其雄激素活性。
J Steroid Biochem Mol Biol. 1997 Jan;60(1-2):121-9. doi: 10.1016/s0960-0760(96)00172-0.
9
7 alpha-Methyl-19-nortestosterone: an ideal androgen for replacement therapy.7α-甲基-19-去甲睾酮：一种用于替代疗法的理想雄激素。
Recent Prog Horm Res. 1994;49:373-6. doi: 10.1016/b978-0-12-571149-4.50027-1.
10
The role of growth hormone in the anabolic action of methandrostenolone.
Endocrinology. 1972 May;90(5):1396-8. doi: 10.1210/endo-90-5-1396.

本文引用的文献

1
A-norprogesterone, an androgen antagonist.去甲孕酮，一种雄激素拮抗剂。
Proc Soc Exp Biol Med. 1960 Jan;103:172-5. doi: 10.3181/00379727-103-25448.
2
Antagonistic action of anti-androgens on the formation of a specific dihydrotestosterone-receptor protein complex in rat ventral prostate.
Mol Pharmacol. 1969 Jul;5(4):428-31.
3
A prostatic cytosol receptor.
Biochem Biophys Res Commun. 1970 Feb 20;38(4):599-606. doi: 10.1016/0006-291x(70)90623-6.
4
An explanation of the antiandrogenic properties of 6 -bromo-17 -hydroxy-17 -methyl-4-oxa-5 -androstane-3-one.
6-溴-17-羟基-17-甲基-4-氧杂-5-雄甾烷-3-酮的抗雄激素特性解释
Steroids. 1972 Sep;20(3):331-43. doi: 10.1016/0039-128x(72)90092-x.
5
[Myotrophic and androgenic activity of certain steroids depending on the duration of action].[某些类固醇的肌营养和雄激素活性取决于作用持续时间]
Probl Endokrinol (Mosk). 1974 Nov-Dec;20(6):60-4.
6
Action of a nonsteroidal antiandrogen, flutamide, on the receptor binding and nuclear retention of 5 alpha-dihydrotestosterone in rat ventral prostate.非甾体类抗雄激素氟他胺对大鼠腹侧前列腺中5α-二氢睾酮受体结合及核内滞留的作用
Endocrinology. 1974 Apr;94(4):1205-9. doi: 10.1210/endo-94-4-1205.