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Research 31–60 of 1000+
- Recent advances in oxasteroids chemistry
- Social isolation alters GABAA receptors plasticity and function: effect of voluntary consumption of ethanol
- Evaluation of New Pregnane Derivatives as 5.ALPHA.-Reductase Inhibitor.
- Steroid Hormones
- Synthesis and Pharmacological Evaluation of New 16-Methyl Pregnane Derivatives.
- Targets to treat androgen excess in polycystic ovary syndrome
- Androgenic and anti-androgenic effects of progesterone derivatives with different halogens as substituents at the C-6 position
- Germacrene Analogs are Anti-androgenic on Androgen-dependent Cells
- Effects of neonatal and adolescent neuroactive steroid manipulation on locomotor activity induced by ethanol in male wistar rats
- Glia-derived steroids modulate epileptogenesis in a model of temporal lobe epilepsy
- TSPO activation modulates the effects of high pressure in a rat ex vivo glaucoma model
- TSPO ligand etifoxine attenuates LPS-induced cognitive dysfunction in mice
- Sex hormones modulate pathogenic processes in experimental traumatic brain injury
- Hormone Blocking Anticancer Drugs
- Ethanol‐induced elevation of 3α‐hydroxy‐5α‐pregnan‐20‐one does not modulate motor incoordination in rats
- Androgen receptor activation integrates complex transcriptional effects in osteoblasts, involving the growth factors TGF-β and IGF-I, and transcription factor C/EBPδ
- Phenytoin‐mediated androgen metabolism in gingival fibroblasts
- Synthesis and Pharmacological Evaluation of New Progesterone Esters as 5.ALPHA.-Reductase Inhibitors
- Synthesis and in Vitro Evaluation of 4-Substituted N-(1,1-Dimethylethyl)-3-oxo-4-androstene-17.beta.-carboxamides as 5.alpha.-Reductase Inhibitors and Antiandrogens
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Synthesis and activity of 8-substituted benzo[c]quinolizin-3-ones as dual inhibitors of human 5α-reductases 1 and 2
- Anti-androgenic curcumin analogues as steroid 5-alpha reductase inhibitors
- A new label-free screen for steroid 5α-reductase inhibitors using LC-MS
- N-Acyl arylsulfonamides as novel, reversible inhibitors of human steroid sulfatase
- Synthesis and 5α-reductase inhibitory activity of 8-substituted benzo[ƒ]quinolinones derived from palladium mediated coupling reactions
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase
- 11α-Hydroxyprogesterone, a potent 11β-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5α-reductase and cytochrome P450 17α-hydroxylase/17,20-lyase to produce C11α-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro