For laboratory research use only. Not for human consumption.

EU
0
Product | GW-501516

GW-501516

GW-501516 (Cardarine) capsules are made with high-quality ingredients to ensure purity and consistency, meeting rigorous standards for quality.

SOLD FOR RESEARCH PURPOSES ONLY

Log in to view prices

What is GW-501516 (Cardarine)?

GW-501516 (known chemically as Cardarine, Endurobol, or GSK-516) is a synthetic, high-affinity small-molecule agonist that selectively targets the peroxisome proliferator-activated receptor delta (PPARδ). Originally codeveloped in the 1990s by GlaxoSmithKline and Ligand Pharmaceuticals to investigate metabolic and cardiovascular pathology, GW-501516 binds the PPARδ ligand-binding domain with sub-nanomolar affinity (EC50 = 1 nM), displaying over 1,000-fold selectivity over PPARα and PPARγ receptor subtypes.

When searching for cardarine for sale or looking to buy gw 501516 online, researchers frequently encounter misclassifications labeling Cardarine as a Selective Androgen Receptor Modulator (SARM) or under queries like cardarine peptide for sale. However, GW-501516 possesses zero androgen receptor binding affinity and contains no amino acid peptide bonds, functioning exclusively as a non-hormonal nuclear receptor transcription factor ligand.

Analytical batch-tested for high chemical purity at Modern Aminos—recognized across independent laboratories as the best place to buy cardarine—GW-501516 is supplied in one laboratory format:

  • 10MG dry-fill solid oral capsules (60 units per bottle)

Laboratories evaluating cellular substrate switching, mitochondrial oxidation, and lipid clearance utilize GW-501516 alongside related metabolic modulators on the site, such as GW-0742, SR-9009, and SLU-PP-332.

Chemical and Molecular Data

Compound Name GW-501516 (Cardarine / Endurobol)
Quantity / Formats Offered 10MG Dry-Fill Capsules (60 Count)
Synonyms / Alt Names Cardarine, Endurobol, GSK-516, GW-1516, GW 501516, GW 50156
CAS Number 317318-70-0
Chemical Formula C21H18F3NO3S2
Molecular Weight 453.50 g/mol
IUPAC Name {2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)sulfanyl]phenoxy}acetic acid
InChIKey YDBLKRPLXZNVNB-UHFFFAOYSA-N
SMILES Code CC1=C(C=CC(=C1)SCC2=C(N=C(S2)C3=CC=C(C=C3)C(F)(F)F)C)OCC(=O)O

What are the Mechanisms of Action?

The biochemical pathways and cellular targets of GW-501516 in laboratory research include:

  • Peroxisome Proliferator-Activated Receptor Delta (PPARδ) Agonism: GW-501516 selectively binds the ligand-binding domain of the nuclear receptor PPARδ. Upon binding, it induces a conformational shift that recruits the Retinoid X Receptor (RXR) heterodimer, activating peroxisome proliferator response elements (PPRE) on target promoter genes.
  • PGC-1α Coactivation & Skeletal Muscle Beta-Oxidation: The PPARδ/RXR complex recruits peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α). This transcriptional cascade upregulates essential fatty acid handling enzymes—including Carnitine Palmitoyltransferase-1 (CPT-1), Fatty Acid Translocase (FAT/CD36), and Pyruvate Dehydrogenase Kinase 4 (PDK4)—shifting myocyte metabolism toward accelerated lipid beta-oxidation.
  • Glycogen Sparing & AMPK Crosstalk: In skeletal muscle cell cultures, Cardarine-mediated fatty acid oxidation spares intracellular glycogen reserves without causing systemic glucose starvation. It activates downstream AMP-activated protein kinase (AMPK) pathways, enhancing basal glucose uptake capacity and mitochondrial respiratory chain output.

What do Preclinical & Academic Studies Show for Cardarine?

When evaluating research efficacy and published scientific literature for gw501516 for sale across reference databases:

  • Structural & Solid-Form Characterization (PMC): Comprehensive analytical investigations cataloged in PMC (PMC11859518) document the X-ray powder diffraction, thermal stability, and solid-state encapsulation kinetics of GW-501516, confirming high chemical stability across lipophilic carriers and organic solvent matrices.
  • Lipid Catabolism and Oxidative Capacity (ScienceDirect): Landmark metabolic assays published in ScienceDirect demonstrate that GW-501516 activates PPARδ gene programs in skeletal muscle cultures, driving type I slow-twitch oxidative muscle fiber conversion and increasing HDL-mediated reverse cholesterol transport in cell models.
  • Chemical Profiling & Identification (PubChem): Official structural characterization maintained on PubChem verifies the molecular mass (453.50 g/mol), trifluoromethyl-thiazole core, and HPLC retention profiles of CAS 317318-70-0.

Comparative Analysis & Product Format

To evaluate formulation parameters, binding affinities, and metabolic pathways, researchers compare GW-501516 against related nuclear receptor agonists:

Dry-Fill Cardarine (Oral Capsules)

The Cardarine format available at Modern Aminos:

  • Dry-Fill Cardarine (Oral Capsules): Formulated as pre-measured 10MG solid dry-fill capsules (60 units per bottle). Provides exact solid-state unit-mass control for analytical weighing, dissolving into custom organic solvent matrices, or dry benchtop storage.

GW-0742 vs GW-501516

Both GW-0742 and GW-501516 (Cardarine) are highly selective PPARδ agonists. GW-0742 is a fluorinated structural analog that exhibits sub-nanomolar binding affinity (EC50 = 0.3 nM), making it slightly more potent in acute in vitro binding assays. However, GW-501516 (EC50 = 1 nM) possesses a significantly larger body of published literature documenting long-term PGC-1α coactivation, making it the preferred gold-standard reference compound for baseline metabolic profiling.

SR-9009 vs Cardarine (GW-501516)

While both compounds are researched as exercise mimetics, their molecular targets are distinct:

  • Cardarine (GW-501516): Directly activates the PPARδ nuclear receptor to recruit PGC-1α, driving skeletal muscle fatty acid beta-oxidation, PDK4 expression, and glucose-sparing pathways.
  • SR-9009 (Stenabolic): Functions as a Rev-Erbα and Rev-Erbβ nuclear receptor agonist. It regulates circadian rhythm gene networks, enhances basal mitochondrial density, and suppresses hepatic lipogenesis through Rev-Erb-dependent transcriptional repression.

SLU-PP-332 vs GW-501516 (Cardarine)

SLU-PP-332 represents a novel class of pan-agonists targeting Estrogen-Related Receptors (ERRα, ERRβ, ERRγ). While GW-501516 targets the PPARδ pathway to stimulate fatty acid transport, SLU-PP-332 directly activates ERR nuclear receptors to drive complex oxidative phosphorylation (OXPHOS) machinery and type IIa oxidative muscle fiber conversion. Researchers frequently compare both compounds to evaluate crosstalk between PPARδ and ERR signaling cascades.

Compound / Reference Primary Target Class Core Mechanism of Action Research Focus & Profile
GW-501516 (Cardarine) PPARδ Selective Agonist Recruits PGC-1α to upregulate skeletal muscle fatty acid beta-oxidation and PDK4 expression Gold-standard research reference for PPARδ-driven lipid catabolism, endurance gene expression, and glucose sparing
GW-0742 PPARδ High-Affinity Agonist Binds PPARδ with sub-nanomolar potency (EC50 = 0.3 nM), featuring a fluorinated structural modification Evaluates rapid PPARδ binding kinetics, acute lipid oxidation, and comparative tissue responses
SR-9009 (Stenabolic) Rev-Erbα / Rev-Erbβ Agonist Binds Rev-Erb nuclear receptors to modulate circadian metabolic gene expression and mitochondrial density Focuses on circadian rhythm regulation, basal metabolic rate elevation, and macrophage inflammatory suppression
SLU-PP-332 Pan-ERR Agonist (ERRα, ERRβ, ERRγ) Directly activates Estrogen-Related Receptors to stimulate PGC-1α and OXPHOS respiratory complexes Focuses on exercise transcription mimetics, type IIa oxidative muscle fiber conversion, and mitochondrial biogenesis

Frequently Asked Questions (FAQs)

1. Is Modern Aminos a reliable place to buy GW-501516?

Yes, Modern Aminos is widely recognized as the premier destination when laboratories seek to buy cardarine or search for cardarine buy online options. Every batch of GW-501516 undergoes strict third-party analytical testing (including HPLC and Mass Spectrometry) to verify minimum 98%+ purity, correct molecular mass (453.50 g/mol), and complete absence of unreacted synthesis precursors or heavy metals.

2. What is the mechanism of Cardarine as a selective PPARδ agonist?

GW-501516 is a selective agonist of the peroxisome proliferator-activated receptor delta (PPARδ). It binds with high affinity (EC50 = 1 nM) to recruit PGC-1α, driving transcription of genes governing fatty acid transport (FAT/CD36) and mitochondrial beta-oxidation (CPT-1, PDK4) in skeletal muscle cell models.

3. Why is Cardarine often mislabeled when researchers search for “cardarine sarm for sale” or “cardarine peptide for sale”?

Despite search terms like “cardarine sarm for sale” or “cardarine peptide for sale”, Cardarine is neither a SARM nor a peptide. It possesses zero binding affinity for androgen receptors and contains no peptide bonds. It is classified chemically as a small-molecule thiazole nuclear receptor ligand that operates strictly through PPARδ metabolic pathways.

4. How does GW-501516 modulate fatty acid beta-oxidation and PGC-1α coactivation?

Upon receptor binding, GW-501516 recruits PGC-1α to increase transcription of Carnitine Palmitoyltransferase-1 (CPT-1) and Pyruvate Dehydrogenase Kinase 4 (PDK4). This causes myocytes to preferentially burn fatty acids for ATP generation rather than glucose, sparing glycogen reserves.

5. What is the cardarine gw 50156 price structure and where to buy cardarine online safely?

At Modern Aminos, researchers can buy gw 501516 online with transparent pricing for 10MG dry-fill capsules (60 count). When evaluating where to buy cardarine or searching gw 50156 for sale, Modern Aminos provides verified COAs.

6. How does GW-501516 compare to GW-0742 and pan-ERR agonists like SLU-PP-332?

GW-0742 is a fluorinated analog with sub-nanomolar PPARδ affinity (EC50 = 0.3 nM), whereas GW-501516 (EC50 = 1 nM) is the most widely cited reference standard. SLU-PP-332 operates through an entirely separate pathway, binding Estrogen-Related Receptors (ERRα/β/γ) to stimulate mitochondrial OXPHOS complexes.

7. What are the proper storage and stability parameters for GW-501516 research reagents?

Capsule containers should be stored tightly sealed in a cool, dry environment (15°C to 25°C) away from direct sunlight, excess heat, and humidity. Stored under controlled laboratory conditions, GW-501516 maintains full chemical stability throughout its designated shelf life.

DISCLAIMER: All compounds and research materials provided by Modern Aminos are strictly for laboratory and research use only. They are not approved for human consumption by the Food and Drug Administration (FDA). No products are approved for oral, sublingual, nor in vivo use. These products should not be used for any form of in vivo experimentation or for any other non-laboratory purpose. Any violation or indication of human or animal use will result in immediate removal from being able to purchase products in the future. By purchasing these products, you acknowledge that they will be used exclusively within a controlled and qualified research environment.

Capsule products are not intended for time-release and are for transport only.

DISCLAIMER: All compounds and research materials supplied by Modern Aminos are intended exclusively for in vitro laboratory research by qualified professionals. They are not medicinal products and have not been authorised by the European Medicines Agency or any national competent authority for human or veterinary use. They are not foods, food supplements, cosmetics or medical devices. Products must not be administered to humans or animals by any route and must not be used for in vivo experimentation or any other non-laboratory purpose. We will refuse or cancel orders, and may close accounts, where there is any indication of human or animal use. By purchasing, you confirm that products will be used only in a controlled laboratory environment by appropriately qualified personnel, in line with all applicable laws.

Related Products

Disclaimer!

All products are sold in powder (lyophilized) form and require reconstitution with a suitable diluent for research purposes only. Research supplies (e.g., syringes, bacteriostatic water) are not included. No dosing instructions are provided. We adhere to all local and state laws around Research Only Chemical sales. We are not a pharmacy, nor do we promote or provide any advice for human or animal consumption. Please review our terms and conditions carefully before making a purchase on our website.

You must be 21+ and a licensed research professional

By clicking ”I Agree” you confirm that you have read and accepted the Terms and Conditions stated above