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Biological activities of a new steroidal inhibitor of delta 4-5 alpha-reductase.

作者信息

Brooks J R, Berman C, Hichens M, Primka R L, Reynolds G F, Rasmusson G H

出版信息

Proc Soc Exp Biol Med. 1982 Jan;169(1):67-73.

PMID:7063497
Abstract
摘要

相似文献

1
Biological activities of a new steroidal inhibitor of delta 4-5 alpha-reductase.一种新型δ4-5α-还原酶甾体抑制剂的生物活性
Proc Soc Exp Biol Med. 1982 Jan;169(1):67-73.
2
Response of rat ventral prostate to a new and novel 5 alpha-reductase inhibitor.大鼠腹侧前列腺对一种新型5α-还原酶抑制剂的反应。
Endocrinology. 1981 Sep;109(3):830-6. doi: 10.1210/endo-109-3-830.
3
Comparison of the effects of the 5 alpha-reductase inhibitor finasteride and the antiandrogen flutamide on prostate and genital differentiation: dose-response studies.5α-还原酶抑制剂非那雄胺和抗雄激素氟他胺对前列腺和生殖器分化影响的比较:剂量反应研究
Endocrinology. 1992 Sep;131(3):1149-56. doi: 10.1210/endo.131.3.1324152.
4
Inhibition of 5 alpha-reductase, receptor binding, and nuclear uptake of androgens in the prostate by a 4-methyl-4-aza-steroid.一种4-甲基-4-氮杂甾体对前列腺中5α-还原酶、雄激素受体结合以及雄激素核摄取的抑制作用
J Biol Chem. 1981 Aug 10;256(15):7998-8005.
5
The effect of a 5 alpha-reductase inhibitor on androgen-mediated growth of the dog prostate.5α-还原酶抑制剂对雄激素介导的犬前列腺生长的影响。
Endocrinology. 1983 Aug;113(2):569-73. doi: 10.1210/endo-113-2-569.
6
Binding of a 4-methyl-4-aza-steroid to 5 alpha-reductase of rat liver and prostate microsomes.
Endocrinology. 1983 Apr;112(4):1460-8. doi: 10.1210/endo-112-4-1460.
7
12. Androgens: Pharmacodynamics and antagonists. Biochemical and biological studies with 4-aza-steroidal 5 alpha-reductase inhibitors.12. 雄激素:药效学与拮抗剂。4-氮杂甾体5α-还原酶抑制剂的生化与生物学研究。
J Steroid Biochem. 1983 Jul;19(1A):385-90. doi: 10.1016/s0022-4731(83)80051-x.
8
Effect of a new 5 alpha-reductase inhibitor on size, histologic characteristics, and androgen concentrations of the canine prostate.一种新型5α-还原酶抑制剂对犬前列腺大小、组织学特征及雄激素浓度的影响
Prostate. 1982;3(1):35-44. doi: 10.1002/pros.2990030107.
9
Effects of an anti-androgen and 5 alpha-reductase inhibitors on estrus duration in the cycling female rat.抗雄激素和5α-还原酶抑制剂对性周期雌性大鼠发情期持续时间的影响。
Physiol Behav. 1983 Apr;30(4):519-24. doi: 10.1016/0031-9384(83)90214-7.
10
Retardation of prostate tumor progression in the Noble rat by 4-methyl-4-aza-steroidal inhibitors of 5 alpha-reductase.5α-还原酶的4-甲基-4-氮杂甾体抑制剂延缓诺布尔大鼠前列腺肿瘤进展
J Natl Cancer Inst. 1985 Feb;74(2):475-86.

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The molecular diversity scope of 1,3-indandione in organic synthesis.1,3-茚二酮在有机合成中的分子多样性范围
Mol Divers. 2016 Feb;20(1):111-52. doi: 10.1007/s11030-015-9589-z. Epub 2015 May 10.
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Novel synthesis of a series of spiro 1,3-indanedione-fused dihydropyridines through the condensation of a tetrone with N-aryl/alkylenamines in presence of solid support silica sulfuric acid.通过在固体载体硅胶硫酸存在下,四酮与N-芳基/亚烷基胺缩合,新型合成一系列螺[1,3-茚二酮并]二氢吡啶。
Mol Divers. 2015 Aug;19(3):459-71. doi: 10.1007/s11030-015-9582-6. Epub 2015 Mar 24.
3
Consideration of the use of 17 beta-N,N-diethylcarbamoyl-4-methyl-4-aza-5- alpha-androstan-3-one (4MA), a 5 alpha-reductase inhibitor, in prostate cancer therapy.
考虑使用5α-还原酶抑制剂17β-N,N-二乙基氨基甲酰基-4-甲基-4-氮杂-5α-雄甾烷-3-酮(4MA)进行前列腺癌治疗。
J Cancer Res Clin Oncol. 1992;118(1):50-5. doi: 10.1007/BF01192311.
4
Inhibition of steroid 5 alpha-reductase by specific aliphatic unsaturated fatty acids.特定脂肪族不饱和脂肪酸对类固醇5α-还原酶的抑制作用。
Biochem J. 1992 Jul 15;285 ( Pt 2)(Pt 2):557-62. doi: 10.1042/bj2850557.