Hupharma sarms Aicar Powder
Nutrobal (Mk-677), S-23, Ostarine (MK-2866), GW-501516 (Cardarine) , RAD140 (Testolone, Radarine, LGD-4033 (Ligandrol, Anabolicum) , DPT130, YK-11, SR9009 (Stenabolic, MELT), Andarine (S-4), Aicar
Name: Aicar
CAS: 2627-69-2
Brand:Hupharma
Synonyms: Acadesine; Aminoimidazole carboxamide ribonucleotide; AICA ribonucleotide
Molecular Formula: C9H15N4O8P
Molecular Weight: 338.211162
Appearance: White Powder
Purity: 99.21%
Melting point: 213-214 °C
Storage: Before reconstitution (lyophilized / freeze dried powder):
Can be stored in the refrigerator (2°C to 8°C = 35°F to 47°F) for 36 months.
Can be stored at room Temperature (up to 37°C = 99°F) for 90 days.
After reconstitution (liquid):
Can be stored in the refrigerator (2°C to 8°C = 35°F to 47°F) for 5 days.
Transportion time at room temperature has not effect on product quality degradation.
Solubility: Soluble in DMSO (15 mg/ml); or water (15 mg/ml).
What Are The Benefits of Aicar?
AICAR will trigger AMP activated protein kinase (AMPK), leading to glucose uptake by cells of skeletal muscle. In fact, The Howard Hughes Medical Center and Salk Institute ran a series of
experiments with AICAR in the 2000’s. In these studies they found out that mice that were given AICAR could run 44% further, even without training for it. Consequently, once endurance athletes got
word of this amazing compound, AICAR was being used without any regulation or fear of testing until 2011.
AICAR works by stimulating the glucose uptake and increasing the activity of p38 mitogen-activated protein kinases a and b in skeletal muscle tissue. Additionally, its reduction of reactive oxygen
compounds within cells suppresses apoptosis; that is, the process of programmed cellular death that may occur in animal test subjects. In other words, it increases the type of fuel responsible for
the maintenance and regulation of skeletal muscle tissue while prolonging the life of cells.
Usages of Aicar
The functionality of AICAR was pinpointed during extensive research conducted by the Salk Institute in 2008, when it conducted a battery of studies on laboratory rats. According to this particular
research, it was determined that the mice that were given AICAR exhibited a significant improvement concerning endurance-type exercise. While the mechanics of this particular improvement were not
isolated and specified, it was theorized that it was due to AICAR's facility for converting fast-twitch muscle fibers to slow-twitch muscle fibers. This conversion in turn allowed for a much
higher rate of energy efficiency amongst the lab rats. Additionally, the scientific tests noted that the conversion also allowed for a more efficient fat burning process amongst the animal test
subjects.