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Nick Mustar, 19
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Dbol Cycle: Guide To Stacking, Dosages, And Side Effects
**An Expert Review of 17α‑Methyltestosterone (17α‑MT) – A Comprehensive Overview for Clinicians and Researchers**
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### 1. Introduction
17α‑Methyltestosterone, commonly known as **17α‑MT** or **17α‑methyltestosterone**, is a synthetic derivative of the endogenous androgen testosterone. By adding a methyl group at the 17α position, the compound gains resistance to hepatic hydroxylation and is thereby orally active—a property that has historically made it attractive for therapeutic use in conditions associated with androgen deficiency.
The drug’s pharmacology is complex: while it retains anabolic properties similar to testosterone, its metabolism generates several intermediates (e.g., 17α‑methyl-5α-dihydrotestosterone) that can exert potent androgenic effects. Consequently, the clinical application of 17α‑MT has been constrained by significant safety concerns, particularly hepatotoxicity and cardiovascular risks.
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## Pharmacokinetics
| Parameter | Description | |-----------|-------------| | **Absorption** | Oral bioavailability is high (~70 %). First‑pass hepatic metabolism accounts for a substantial portion of dose conversion to active metabolites. | | **Distribution** | Protein binding ~70–80 %. Lipophilic metabolites cross cell membranes readily, facilitating action in target tissues (skin, prostate). | | **Metabolism** | Predominantly hepatic via cytochrome P450 enzymes (CYP3A4/5) converting to 17‑α‑hydroxylated derivatives. Metabolites retain androgenic activity. | | **Elimination** | Excreted mainly in feces; minor urinary excretion (~10 %). Terminal half‑life ~6–8 h, but sustained tissue retention of metabolites extends effect. |
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## 4. Clinical Applications
### 4.1 Dermatology – Acne Vulgaris (Topical)
| **Evidence** | **Key Findings** | |--------------|------------------| | *Randomized controlled trials* (RCTs) comparing topical clascoterone vs placebo or other topical retinoids (e.g., adapalene). | - Significant reduction in inflammatory lesions after 12 weeks. - Similar efficacy to adapalene but without irritation. | | Systematic reviews of clascoterone 1% gel/cream. | - Demonstrated a favorable benefit‑risk profile, especially for patients with sensitive skin or rosacea‑prone skin. |
**Clinical Implication:** Clascoterone is an effective alternative for mild‑to‑moderate acne where retinoids are contraindicated.
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#### 2.4 Adverse Events and Tolerability
| Adverse Event | Frequency (reported in clinical trials) | |---------------|----------------------------------------| | Burning/irritation |
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