Azasteroids: structure-activity relationships for inhibition of 5 alpha-reductase and of androgen receptor binding.
about
Clinical application of 5alpha-reductase inhibitors.N-tert-Butyl-3-hydr-oxy-5-androstene-17-carboxamide monohydrate.Intratumoral steroidogenesis in castration-resistant prostate cancer: a target for therapy.Calcium- and voltage-gated potassium (BK) channel activators in the 5β-cholanic acid-3α-ol analogue series with modifications in the lateral chainFeed-forward control of prostate growth: dihydrotestosterone induces expression of its own biosynthetic enzyme, steroid 5 alpha-reductasePreventing diseases of the prostate in the elderly using hormones and nutriceuticals.Mechanism based inhibition of hydroxysteroid dehydrogenases.Identification and selective inhibition of an isozyme of steroid 5 alpha-reductase in human scalp.Therapeutic options in the treatment of benign prostatic hyperplasia.Advances in the design and discovery of drugs for the treatment of prostatic hyperplasia.Potential targets in the discovery of new hair growth promoters for androgenic alopecia.Adverse effects of 5α-reductase inhibitors: What do we know, don't know, and need to know?The new insight of prostate-specific antigen reduction during finasteride therapy in aging men.Finasteride inhibits 5 alpha-reductase activity in human dermal fibroblasts: prediction of its therapeutic application in androgen-related skin diseases.The role of transforming growth factor-beta1, -beta2, and -beta3 in androgen-responsive growth of NRP-152 rat prostatic epithelial cells.Intramolecular Pd-catalyzed carboetherification and carboamination. Influence of catalyst structure on reaction mechanism and product stereochemistry.Effect of finasteride on serum prostate-specific antigen (PSA) and on prostate of hamster Mesocricetus auratus (hMa).Linear relationships between the ligand binding energy and the activation energy of time-dependent inhibition of steroid 5alpha-reductase by delta 1-4-azasteroids.Relative binding affinity of novel steroids to androgen receptors in hamster prostate.Novel inhibitors of 5α-reductase
P2860
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P2860
Azasteroids: structure-activity relationships for inhibition of 5 alpha-reductase and of androgen receptor binding.
description
1986 nî lūn-bûn
@nan
1986 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Azasteroids: structure-activit ...... of androgen receptor binding.
@ast
Azasteroids: structure-activit ...... of androgen receptor binding.
@en
Azasteroids: structure-activit ...... of androgen receptor binding.
@nl
type
label
Azasteroids: structure-activit ...... of androgen receptor binding.
@ast
Azasteroids: structure-activit ...... of androgen receptor binding.
@en
Azasteroids: structure-activit ...... of androgen receptor binding.
@nl
prefLabel
Azasteroids: structure-activit ...... of androgen receptor binding.
@ast
Azasteroids: structure-activit ...... of androgen receptor binding.
@en
Azasteroids: structure-activit ...... of androgen receptor binding.
@nl
P2093
P356
P1476
Azasteroids: structure-activit ...... of androgen receptor binding.
@en
P2093
Cascieri MA
Rasmusson GH
Reynolds GF
Steinberg NG
P304
P356
10.1021/JM00161A028
P407
P577
1986-11-01T00:00:00Z