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While it has gained popularity due to its ability to stimulate fat metabolism without increasing IGF-1 levels, its essential to understand how it differs from other peptides like hGH, CJC-1295, Ipamorelin, and Semaglutide (Ozempic)

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Through DNA damage, lipid peroxidation, protein oxidation, and the release of pro-inflammatory factors, CSD would disrupt hepatic cellular membrane integrity and alter the structural proteins of iron channels, leading to Fe 2+ overload and exacerbating the oxidative stress-mediated ferroptotic changes (8, 25, 26)