Comparison

Melatonin

Item no. CS-1769-500mg
Manufacturer ChemScene
Amount 500mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias 73-31-4
Similar products 73-31-4
Available
Alternative Names
N-Acetyl-5-methoxytryptamine
CAS
73-31-4
Purity
>98%
MWt
232.28
Formula
C13H16N2O2
Solubility
DMSO : 100 mg/mL (430.51 mM; Need ultrasonic); Ethanol : >= 50 mg/mL (215.26 mM)
Clinical Information
Launched
Pathway
GPCR/G Protein; Neuronal Signaling; Autophagy; Autophagy; Metabolic Enzyme/Protease
Target
Melatonin Receptor; Melatonin Receptor; Autophagy; Mitophagy; Endogenous Metabolite
Biological Activity
Melatonin is a hormone made by the pineal gland that can activates melatonin receptor. Melatonin plays a role in sleep and possesses important antioxidative and anti-inflammatory properties[1][2][3]. Melatonin is a novel selective ATF-6 inhibitor and induces human hepatoma cell apoptosis through COX-2 downregulation[4]. Melatonin attenuates palmitic acid-induced (HY-N0830) mouse granulosa cells apoptosis via endoplasmic reticulum stress[5]. In Vivo: Melatonin increases the levels of activated PTEN, RSK-1, mTOR and AMPKalpha kinases, mildly inhibits ERK-1/2 phosphorylation and Bad phosphorylation, significantly inhibits phosphorylations of S6 Ribosomal Protein, 4E-BP1, GSK-3alpha and GSK-3beta, and slightly increases PRAS40 phosphorylation in animals[1]. Melatonin ameliorates the neurotoxiciy and astrocyte activation induced by Abeta1-42 in the cerebral cortex. Melatonin also blocks the reduction in Reelin and Dab1 expression induced by Abeta1-42[2]. Melatonin treatment and lack of NLRP3-/- share similar inhibition of NF-kappaB and NLRP3 signaling pathway in mice. Melatonin treatment and lack of NLRP3-/- share some patterns of clock genes expression, and improve cardiomyocytes morphology in mice[3].
Research Area
Cancer; Inflammation/Immunology; Neurological Disease

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Amount: 500mg
Available: In stock
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