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6-hydroxy Melatonin is an active metabolite of melatonin (Cay-14427). It is formed from melatonin by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. 6-hydroxy Melatonin is a melatonin 1A (MT1A), MT1B, and MT2 receptor agonist. It inhibits dopamine release from isolated rabbit retina (IC50 = 0.0016 µM). 6-hydroxy Melatonin (10 and 100 µM) reduces increases in the levels of NF-kappaB, IL-6, and IL-8 and decreases in glutathione (GSH) levels in LPS- and peptidoglycan G-stimulated human umbilical vein endothelial cells (HUVECs) in an in vitro model of sepsis. It reduces iron-induced lipid oxidation in rat hippocampal homogenate when administered at a dose of 10 mg/kg.Formal Name: N-[2-(6-hydroxy-5-methoxy-1H-indol-3-yl)ethyl]-acetamide. CAS Number: 2208-41-5. Synonyms: 6-OHM. Molecular Formula: C13H16N2O3. Formula Weight: 248.3. Purity: >95%. Formulation: (Request formulation change), A crystalline solid. Solubility: DMF: 30 mg/ml, DMSO: 30 mg/ml, DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml, Ethanol: 20 mg/ml. lambdamax: 219, 303 nm. SMILES: COC1=C(O)C=C(NC=C2CCNC(C)=O)C2=C1. InChi Code: InChI=1S/C13H16N2O3/c1-8(16)14-4-3-9-7-15-11-6-12(17)13(18-2)5-10(9)11/h5-7,15,17H,3-4H2,1-2H3,(H,14,16). InChi Key: OMYMRCXOJJZYKE-UHFFFAOYSA-N.
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