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Avodart 0,5 mg GSK

GSK

45,00

In Stock (100 available)

Avodart 0,5 mg GSK (0,5 mg) — This GSK formulation delivers this pharmaceutical-grade injectable compound is formulated for optimal bioavailability through intr…

100 in stock

This product is for laboratory research use only. Not for human consumption.

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Description

Avodart 0,5 mg GSK — dutasteride from GSK at 0.5 mg. Dual 5α-reductase inhibitor (types I + II). ~90% DHT reduction vs finasteride‘s ~70%. 5-week half-life — effects build and wash out slowly.

Key Benefits

  • 5α-reductase type-I AND type-II inhibitor — more complete than finasteride
  • Suppresses scalp DHT ~95% (vs finasteride ~70%)
  • Clinical standard for more aggressive androgenic-alopecia cases
  • Oral once-daily; long half-life
  • Not effective against DHT-derivative AAS (tren, masteron, oxandrolone)
  • Each unit dosed at 5 mg — see Recommended Dosage below for protocol-specific intake

Recommended Dosage

Clinical dosing: 0.5 mg/day for hair-loss prevention / BPH. Loading not required — steady-state develops over 3–6 months due to long half-life. Some hair-loss protocols dose every other day to reduce cost.

How It Works

Dual 5α-reductase inhibitor (both type I and type II isoforms). More comprehensive DHT suppression than finasteride (type II only). Oral bioavailability ~60%, extensive protein binding.

Pharmacokinetics

Plasma half-life approximately 5 weeks — extremely long. Once-daily dosing but steady-state takes 3–6 months. Tissue DHT suppression persists weeks after discontinuation.

Potential Side Effects

Sexual side-effects (libido drop, ED) similar rate to finasteride. Post-finasteride syndrome documented but rare. Gynecomastia rare but possible. Does NOT protect against DHT-derivative AAS — separate mechanism.

Cycle & Stacking Guide

Long-term use for hair protection during testosterone-based cycles. Pointless alongside tren, masteron, oxandrolone, or winstrol — those bypass 5α-reductase entirely.

Manufacturer Notes

GSK is an independent producer in the research-compound market. Before first use, request the batch-specific Certificate of Analysis and confirm the vial’s tamper-evident seal is intact.

Storage & Handling

Store at recommended temperature (15–25°C; peptides and HGH at 2–8°C after reconstitution). Protect from light and moisture. Keep out of reach of children. For research and educational purposes only.

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Dutasteride

Physical & Chemical Properties for Research Purposes
Chemical structure of Dutasteride (C27H30F6N2O2) for laboratory analysis
2D structural representation · PubChem CID 152945 ↗
Chemical Identity
# CAS Registry Number 164656-23-9
Σ IUPAC Name (5alpha,17beta)-N-[2,5-bis(trifluoromethyl)phenyl]-3-oxo-4-azaandrost-1-ene-17-carboxamide
F Molecular Formula C27H30F6N2O2
M Molecular Weight 528.53 g/mol
SMILES FC(F)(F)C1=CC=C(C(F)(F)F)C(NC(=O)[C@H]2CC[C@@H]3[C@@]2(C)CC[C@H]4[C@H]3CC[C@@H]5NC(=O)C=C[C@]45C)=C1
InChIKey JWJOTENAMICLJG-QWBYCMEYSA-N
Melting Point 242-250 °C
Solubility Freely soluble in ethanol, methanol; practically insoluble in water
Biological Half-life 5 weeks (oral)
PubChem CID 152945 ↗
Pharmacological Profile
Aromatization None
Hepatotoxicity Low
Known trade names: Avodart, Dutasteride, Duagen

Data sourced from published pharmacological literature and authoritative chemical databases (PubChem, DrugBank, ChEBI). Provided for identification and research reference only.