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acetaminophen glutathione conjugate 3-(glutathion-S-yl)acetaminophen | C18H24N4O8S | CID 83998 acetaminophen toxicity mechanism

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Chemisches Profil Molekularformel: C43H66N12O12S2 Molekulargewicht: 1007.19 g/mol Peptidtyp: Nonapeptid-Hormon Alternative Namen: Rekombinantes Oxytocin, Endopituitrin Wirkmechanismus (forschungsbasiert) Forscher gehen davon aus, dass Oxytocin primär an G-Protein-gekoppelte Rezeptoren (GPCRs) bindet und dadurch intrazelluläre Calcium-Signalwege aktiviert

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There is no New Drug Application (NDA), Biologics License Application (BLA), or 510(k) clearance associated with this compound for human therapeutic use.[1] What GHK-Cu actually is, pharmacologically, is a tripeptide (Gly-His-Lys) bound to copper(II) ions, with a molecular weight of approximately 340.38 g/mol for the free tripeptide and around 403.9 g/mol for the copper complex

acetaminophen glutathione conjugate 3-(glutathion-S-yl)acetaminophen | C18H24N4O8S | CID 83998 acetaminophen toxicity mechanism

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