Nandrolone Phenpropionate
Nandrolone Phenpropionate Uses, Dosage, Side Effects, Food Interaction and all others data.
C18 steroid with androgenic and anabolic properties. It is generally prepared from alkyl ethers of estradiol to resemble testosterone but less one carbon at the 19 position. It is a schedule III drug in the U.S.
Nandrolone is an anabolic steroid occurring naturally in the human body, albeit in small quantities. Nandrolone increases production and urinary excretion of erythropoietin. It may also have a direct action on bone marrow. Nandrolone binds to the androgen receptor to a greater degree than testosterone, but due to its inability to act on the muscle in ways unmediated by the receptor, has less overall effect on muscle growth.
Trade Name | Nandrolone Phenpropionate |
Generic | Nandrolone phenpropionate |
Nandrolone phenpropionate Other Names | 19NTPP, Nadrolone phenylpropionate, Nandrolon phenylpropionate, Nandrolone phenpropionate, Nandrolone phenylpionate, Nandrolone phenylpropionate, Norandrolone phenyl propionate, Norandrostenolone phenylpropionate, Nortestosterone phenylpropionate, NTPP |
Type | |
Formula | C27H34O3 |
Weight | Average: 406.5571 Monoisotopic: 406.250794954 |
Protein binding | 58% |
Groups | Approved, Illicit, Investigational |
Therapeutic Class | |
Manufacturer | |
Available Country | |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
For the treatment of refractory deficient red cell production anemias, breast carcinoma, hereditary angioedema, antithrombin III deficiency, fibrinogen excess, growth failure and Turner's syndrome. It is also indicated in the prophylaxis of hereditary angioedema.
How Nandrolone Phenpropionate works
Nandrolone is an androgen receptor agonist. The drug bound to the receptor complexes which allows it to enter the nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects.
Elimination Route
The absorption after oral dosing is rapid for testosterone and probably for other anabolic steroids, but there is extensive first-pass hepatic metabolism for all anabolic steroids except those that are substituted at the 17-alpha position. The rate of absorption from subcutaneous or intramuscular depots depends on the product and its formulation. Absorption is slow for the lipid-soluble esters such as the cypionate or enanthate, and for oily suspensions.
Half Life
The elimination half-life from plasma is very short.
Innovators Monograph
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