RAD 140 Description:
RAD140 is a highly effective, oral SARM (Selective Androgen Receptor Modulators) currently being studied for both anabolic and neuroprotective effects. It is in the class of androgen receptor (AR) ligands, which are tissue selective, developed to treat cancer-related muscle wasting, acute and chronic disease, and age-related muscle loss. Recent RAD140 research shows higher lean tissue selectivity and reduced androgenic side effects compared to competing Šarm compounds. T
his compound is being tested for neuroprotection as well; An important neuronal action of endogenous androgens, which are essential to nervous health and immunity to neurodegenerative diseases, and to be as effective as testosterone in reducing cell death induced by apoptotic insults. An easy-to-dose oral Sarm that increases the mass of lean tissue while remaining selective in this research-added value for studies with pronounced Myotrophic neuroprotective properties and a research compound of neuroregeneration.
RAD 140 Application:
According to a Cambridge-based pharmaceutical company, RAD 140 SARM is potent, orally biologically and non-steroidal, designed to make the hormone receptors in the body’s tissues work in the same way as if you are getting a good dose of testosterone, prescribing the same effects as if you were cycling from prohormones and anabolic steroids minus unwanted side effects.
In addition, clinical studies have also shown that RAD 140 SARM also has several other advantages that we will discuss in more detail in a moment.
Increased speed, endurance, and endurance during high-intensity workoutsFaster build-up of muscle tissue, which helps you achieve more gains in a shorter time-based period on medical research, RAD 140 SARM displayed a greater anabolic effect than testosterone used. The researchers emphasize that in addition to having a more “enhanced” effect than testosterone, RAD 140 SARM has also been observed to help reduce androgenic side effects that can potentially be caused by the same on the prostate.