The compound has not progressed through a drug-approval pathway in any major jurisdiction
Do not attempt to manage them at home
Product Attributes CAS # : 221231-10-3 Molecular Formula : C78H123N23O23S2 Sequence (AA) : YLRIVQCRSVEGSCGF (with disulfide bond between Cys-7 and Cys-14) Molecular Weight : 1815.1 g/mol PubChem CID : 71300630 Half-Life : ~4-6 hours Synonyms : Anti-Obesity Drug 9604, hGH Fragment 176-191, Lipolytic hGH Fragment, Tyr-hGH (177-191), Tyr-somatostatin Type : Synthetic research peptide (growth hormone fragment) Research Focus : Weight Loss & Metabolic Regulation Scientific References Metabolic studies of a synthetic lipolytic domain (AOD9604) of human growth hormone Animal The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta(3)-AR knock-out mice Animal Safety and tolerability of the hexadecapeptide AOD9604 in humans Human RCT Safety and metabolism of AOD9604, a novel nutraceutical ingredient for improved metabolic health Human RCT | Observational | Animal | In vitro Obesity pharmacotherapy: current perspectives and future directions Human RCT Effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism Animal | In vitro Obesity drugs in clinical development Human RCT Recent advances in the pathophysiology and pharmacological treatment of obesity Human RCT | Observational Potential role of new therapies in modifying cardiovascular risk in overweight patients with metabolic risk factors Observational Peptides: AOD-9604 & BPC-157 Human RCT | Animal | In vitro Included In The Box Every product arrives in a premium, custom-designed PEPTIDE.Power box , engineered for convenience, hygiene, and safe storage in your refrigerator
Those with diseases that affect the gut, such as Crohns disease or celiac disease, are also at risk ( Summary Those at greatest risk of vitamin B12 deficiency are vegans and vegetarians, who get little to no B12 from the diet
The compound enters the bloodstream, distributes to tissues based on perfusion rates and partition coefficients, and reaches target cells without the absorption and metabolism bottlenecks that plague oral routes
