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oralanabolic

Norethandrolone

NilevarNorethandrolone
125
Anabolic Ratio
37
Androgenic Ratio
0.42d
Half-Life

One of the first synthetic anabolic steroids developed (1956), predating Dianabol. A 19-nor compound (related to nandrolone) with an ethyl group at C17. Historically used for anemia and muscle wasting. Notable for being the first synthetic progestogen to show potent anabolic properties. Now largely replaced by safer alternatives.

Mechanism of Action

19-nortestosterone derivative — reduced androgenicity due to 5α-reduction to a less active metabolite in androgenic tissue. Moderate progestogenic activity (as a 19-nor). 17α-ethyl group provides oral bioavailability. Aromatizes to 17α-ethyl estradiol. Similar suppression profile to nandrolone.

Norethandrolone molecule
Molecular structure

Typical Dosing

140 mg
low / week
280 mg
moderate / week
490 mg
high / week

⚠ Warning Flags

  • Largely obsolete — replaced by safer 19-nor compounds
  • Oral 17α-alkylated hepatotoxicity
  • Prolactin elevation risk (19-nor class)

Effect Profile

Muscle Protein Synthesis
5Moderate
Nitrogen Retention
6Moderate
Strength Gains
5Moderate
Red Blood Cell Production
5Moderate
Fat Loss
3Low
Glycogen Storage
5Moderate
Recovery Speed
5Moderate
Collagen Synthesis
5Moderate

Side Effect Profile

Hormonal Suppression
7High
Estrogenic Effects
4Low
Androgenic Effects
3Low
Cardiovascular Strain
4Low
Liver Stress
5Moderate
Insulin Resistance
2Minimal
Mood Changes
4Low
Prostate Risk
2Minimal

Research Studies

The myotrophic and androgenic effects of 17-ethyl-19-nortestosterone and related compounds

Saunders FJ, Drill VA. · 1956

PubMed

Original pharmacological characterization of norethandrolone, establishing its anabolic-to-androgenic differentiation (Hershberger assay) and superior anabolic selectivity versus testosterone — one of the foundational papers in AAS pharmacology.