Description
(18-35 year old demographic)
LIQUID OSTARINE (MK-2866) – THE ULTIMATE GUIDE
Ostarine, also known as MK-2866, GTX-024, or Enobosarm, is one of the most well-researched and widely recognized selective androgen receptor modulators (SARMs). Originally developed in the late 1990s, Ostarine was designed as a potential treatment for conditions like osteoporosis, muscle wasting, and insulin resistance. Today, it remains a focal point of clinical research due to its unique ability to selectively target androgen receptors without the harsh side effects commonly associated with anabolic steroids, testosterone, or human growth hormone.
WHY OSTARINE STANDS OUT IN CLINICAL RESEARCH
Ostarine’s selective action makes it a promising candidate for research, particularly in female and elderly populations where traditional anabolic treatments may not be suitable. Studies have shown that Ostarine is generally well-tolerated, with doses of up to 18mg per day administered safely over 12 months in female cancer patients. Unlike many anabolic agents, Ostarine is orally bioavailable, eliminating the need for injections.
While Ostarine shows significant potential, it’s important to note that research is ongoing. Potential side effects, such as testosterone suppression in males and menstrual irregularities in females, are still being studied. Long-term effects and interactions with other substances remain under investigation.
POTENTIAL BENEFITS OF OSTARINE IN RESEARCH STUDIES
Research on Ostarine has highlighted several potential benefits, including:
- Enhanced muscle growth and strength
- Increased protein synthesis
- Improved bone density and health
- Accelerated recovery of connective tissues
- Reduction in body fat and support for weight loss
- Boosted energy levels
- Positive effects on heart health
It’s crucial to emphasize that Ostarine is not approved by the FDA for human consumption and is strictly intended for laboratory research purposes. It should not be confused with dietary supplements or sports performance enhancers.
KEY RESEARCH FINDINGS ON OSTARINE (MK-2866)
- Muscle and Strength Benefits: A 2011 study demonstrated that Ostarine significantly increased lean body mass, muscle strength, and physical function in elderly men and postmenopausal women.
- Bone Health: A 2019 study on ovariectomized rats found that Ostarine improved bone healing and stimulated muscle growth.
- Fat Metabolism: Research on Wistar rats revealed that Ostarine reduced fat-mediating hormones like leptin, suggesting potential benefits for fat loss.
- Osteoporosis Support: Another 2019 study showed that Ostarine increased bone mineral density and reduced osteoporosis symptoms in postmenopausal rat models.
POTENTIAL SIDE EFFECTS AND SAFETY CONSIDERATIONS
As one of the oldest and most studied SARMs, Ostarine has a well-documented profile. However, research is still uncovering its full range of effects. Potential side effects may include:
- Testosterone suppression in males
- Menstrual irregularities in females
- Possible liver strain or increased hematocrit levels
- Insomnia or lethargy in some cases
The FDA has issued warnings about the misuse of Ostarine, emphasizing that it is not approved for human use and may pose serious health risks if abused.
LIQUID OSTARINE (MK-2866) PRODUCT DETAILS
- CAS Number: 841205-47-8
- Molecular Formula: C19H14F3N3O3
- Molar Mass: 389.330 g/mol
- Half-Life: 24 hours
- Classification: Selective Androgen Receptor Modulator (SARM)
Product Specifications:
- 30ml liquid Ostarine per bottle
- Concentration: 25mg per milliliter
- Includes a graduated 1mL glass pipette for precise measurement
- UV-resistant glass bottle to minimize degradation
- Tamper-proof seal for safety during transit
- Less than 5% variance in concentration for consistent results
- Formulated to prevent evaporation during storage
Storage Instructions: Store in a cool, dry place away from direct sunlight to maintain optimal shelf life.
Disclaimer: This product is intended for laboratory research purposes only. It is not approved for human consumption, nor is it a dietary or sports supplement.
REFERENCES
- Dalton JT, et al. (2011). The selective androgen receptor modulator GTx-024 (enobosarm) improves lean body mass and physical function in healthy elderly men and postmenopausal women. PubMed.
- Hoffmann DB, et al. (2019). Evaluation of ostarine as a selective androgen receptor modulator in a rat model of postmenopausal osteoporosis. PubMed.
- Smith MR, et al. (2019). A Phase II Clinical Trial of Pembrolizumab and Enobosarm in Patients with Androgen Receptor-Positive Metastatic Triple-Negative Breast Cancer. PubMed.
- Effect of ostarine (enobosarm/GTX024) on adipocyte metabolism in Wistar rats. PubMed.
(18-35 year old demographic)
Liquid Cardarine (GW501516) Overview – Elitebiogenix.com
Cardarine, scientifically known as GW501516 or Endurobol, is a potent PPAR (peroxisome proliferator-activated receptor) agonist. This compound functions as a ligand-activated transcription factor, binding to receptors in skeletal muscle and adipose tissue, promoting lipid utilization and fat burning. PPARs are also integral to processes like inflammation regulation, glucose homeostasis, and cellular functions such as proliferation, differentiation, and apoptosis, hinting at potential anti-aging benefits [1].
PPARs are predominantly found in tissues with high metabolic activity, including skeletal muscle, liver, heart, kidneys, and intestines [13]. Although often mistakenly grouped with selective androgen receptor modulators (SARMs), GW501516 operates differently. It does not interact with androgen receptors or influence testosterone levels but plays a significant role in energy metabolism.
How Cardarine Works
Developed in the 1990s, Cardarine is also referred to as GW1516 and GSK-516. It exhibits strong affinity (Ki = 1 nM) and specificity for PPARδ, with over 1,000-fold selectivity compared to PPARα and PPARγ [5]. When GW501516 binds to PPARδ, it recruits the coactivator PGC-1α, forming a complex that enhances the expression of proteins involved in energy expenditure [6]. By activating AMP-activated protein kinase, Cardarine is believed to offer a range of experimental benefits, including:
- Boosting fatty acid oxidation and fat loss
- Reducing LDL (“bad”) cholesterol
- Increasing HDL (“good”) cholesterol
- Enhancing endurance and stamina
- Lowering inflammation
- Improving insulin sensitivity and glucose tolerance
The Role of PPAR Agonists
Research shows that PPAR activity helps preserve glucose for critical tissues like the brain while mobilizing fatty acids for muscle endurance [10]. PPARs also regulate temperature, inflammation, mitochondrial respiration, and tissue repair. Molecular studies indicate that PPARs control genes linked to lipid oxidation, mitochondrial biogenesis, and contractile proteins [10].
PPAR Effects During Fasting
PPARs are particularly active during fasting, when free fatty acids are released into the bloodstream. Studies on PPAR-null mice revealed that the absence of PPAR leads to elevated free fatty acids, lipid accumulation in the liver and heart, low blood sugar, reduced body temperature, ketone production, and premature death [14]. Mice adapt to fasting by upregulating PPAR genes, which enhance fatty acid uptake and oxidation [15].
Cardarine Research Findings
Numerous animal studies highlight Cardarine’s potential to improve energy metabolism and blood lipid profiles:
- A study on mice demonstrated that GW501516 enhances fatty acid oxidation and alleviates metabolic syndrome [1].
- Research on Kunming mice showed that PPAR activation significantly boosts running endurance [2].
- Another study found that PPARs prevent glucose depletion during exercise, delaying fatigue [3].
- In obese rhesus monkeys, GW501516 increased HDL and reduced VLDL, suggesting cardioprotective effects [6].
- Phase II clinical trials indicated Cardarine’s potential benefits for obesity, diabetes, dyslipidemia, and cardiovascular health, along with reduced inflammation [7, 8].
- A study on high-fructose-fed rats found that GW501516 lowered inflammation markers and upregulated genes involved in beta-oxidation [11].
Cardarine Side Effects
While Cardarine does not cause androgenic side effects like steroids, high doses (3mg/kg/day) in rats led to rapid cancer development in multiple organs [9]. Anecdotal reports suggest minimal side effects, but further research is needed to establish its safety profile. The FDA has not approved Cardarine for human use, and it is banned by the World Anti-Doping Agency (WADA) due to its endurance-enhancing properties [4].
Liquid Cardarine Specifications
- CAS Number: 317318-70-0
- Formula: C21H18F3NO3S2
- Molar Mass: 453.498 g/mol
- Half-Life: 16–24 hours
- Class: PPAR Agonist
- Storage: Store in a cool, dry place away from sunlight to maintain potency.
Product Details:
- 30ml liquid Cardarine per bottle (20mg/ml concentration)
- UV-resistant glass bottle to minimize degradation
- Tamper-proof seal for secure delivery
- Less than 5% concentration variance for consistency
- Formulated to prevent evaporation during storage
Important Note:
This product is strictly for laboratory research purposes and is not approved by the FDA for human consumption. Cardarine (GW501516) is not a dietary or sports supplement.
Scientific References:
- Tanaka et al., Proc. Natl. Acad. Sci. U.S.A., 2003
- Chen et al., Sci. Rep., 2015
- Fan et al., Cell Metab., 2017
- Sports Technology Labs, 2023
- Oliver et al., Proc. Natl. Acad. Sci. U.S.A., 2001
- Sprecher, Am J Cardiol., 2007
- Barish et al., J Clin Invest., 2006
- Dressel et al., Mol Endocrinol., 2003
- Sahebkar et al., Expert Opin Pharmacother., 2014
- Coll et al., Endocrinology, 2010
- Magliano et al., Endocrine, 2015
- Van Wagoner et al., JAMA, 2017
- Burri et al., PPAR Res., 2010
- Leone et al., Proc. Natl. Acad. Sci. U.S.A., 1999
- Kersten et al., J Clin Invest., 1999
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