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1-Monomyristin

1-Monomyristin

Item no.	HY-N2512-5mg
Manufacturer	MedChem Express
CASRN	589-68-4
Amount	5 mg
Quantity options	10mM/1mL 10 mg 20 mg 5 mg
Category	Inhibitors & Compound Libraries Small Molecules
Type	Inhibitors
Specific against	other
Purity	98.0
Formula	C17H34O4
Citations	[1]Shimada H, et al. Biologically active acylglycerides from the berries of saw-palmetto (Serenoa repens). J Nat Prod. 1997 Apr;60(4):417-8.<br/>[2]Vandevoorde S, et al. Influence of the degree of unsaturation of the acyl side chain upon the interaction of analogues of 1-arachidonoylglycerol with monoacylglycerol lipase and fatty acid amide hydrolase. Biochem Biophys Res Commun. 2005 Nov 11;337(1):104-9.<br/>[3]Jumina, et al. Monomyristin and Monopalmitin Derivatives: Synthesis and Evaluation as Potential Antibacterial and Antifungal Agents. Molecules. 2018 Nov 29;23(12). pii: E3141
Smiles	CCCCCCCCCCCCCC(OCC(O)CO)=O
ECLASS 10.1	32160490
ECLASS 11.0	32160490
UNSPSC	12000000
Alias	589-68-4
Available
Product Description	1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3].
StorageTemperature	-20°C, 3 years; 4°C, 2 years (Powder)
Shipping	Room Temperature
Manufacturers Applications	COVID-19-immunoregulation
MolecularWeight	302.45
Clinical Information	No Development Reported
Manufacturers Research Area	Infection
Solubility	DMSO : 100 mg/mL (ultrasonic)
Target	Autophagy; Bacterial; Endogenous Metabolite; FAAH; Fungal
Manufacturers Target	Autophagy; Bacterial; Endogenous Metabolite; FAAH; Fungal
Isoform	Human Endogenous Metabolite
Manufacturers Pathway	Anti-infection; Autophagy; Metabolic Enzyme/Protease; Neuronal Signaling
Manufacturers Product type	Natural Products

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