Its a progestin, like any Nandrolone derivative, and is made by removing the carbon atom at the 19th position of the Steran Nucleus of testosterone. However, although its a progestin, Nandrolone (regardless of ester) doesnt produce much of what we could properly call estrogenic side effects. Any side effects from NandrolonePhenylpropionate would therefore more properly be termed progestenic in nature- as it only converts to estrogen at roughly 20% the rate of testosterone.
Regardless of ester, and water retention not withstanding, we find that all of the characteristics of found in one type of Nandrolone are found in any other. Nandrolone, probably owing to its progestenic nature has the ability to improve collagen synthesis as well as bone mineral content. Clearly this would be a huge benefit to athletes with connective tissue problems or other joint issues, although drug-tested athletes need to avoid Nandrolones because of their detectability in urine for a year to eighteen months after administration. Also, since it is progestin (with slight estrogenic ability), it probably has some very beneficial effects on the immune mediated anti-inflammatory process, thereby soothing joints as well as helping to heal them.
Nandrolone is one of the few steroids which has been used successfully in AIDS patients to stimulate weight gain, and although athletes using NPP in lieu of Deca find it to produce slightly less weight gain, this is probably a result of gaining less water weight. NandrolonePhenylpropionate, is a more popular drug than Deca for use in cutting cycles recently, due to this fact.
This brings up the fact that although Deca has a very long active life, NPP has a much shorter one, and this means that people are forced to inject at least two times per week, with the more common protocol being every third day. Results are seen much more quickly with NPP as compared with Deca, and its quickly becoming a much more popular alternative.
Possible Side effects: Because nandrolone is not broken down into DHT, the deleterious effects to most anabolic steroids on the scalp, skin, and prostate are lessened to a degree; but is rather broken down to the much weaker androgen dihydronandrolone. The lack of alkylation on the 17a-carbon drastically reduces the drug’s liver toxicity. Estrogenic effects resulting from reaction with aromatase are also mitigated as a result of the drug being a progestin, but effects such as gynecomastia and reduced libido still occur in larger doses. Other side-effects can include erectile dysfunction and cardiovascular damage, as well as several ailments resulting from the drug’s effect of lowering levels of luteinizing hormone through negative feedback.
Effective dose: 50 – 150 mg in every other day