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1-Monomyristin

CAT: 0804-HY-N2512-01Size: 25 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-N2512-01Size:25 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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].
CAS Number
589-68-4
UNSPSC
12352211
Hazard Statement
H302, H315, H319, H335
Target
Autophagy; Bacterial; Endogenous Metabolite; FAAH; Fungal
Type
Natural Products
Related Pathways
Anti-infection; Autophagy; Metabolic Enzyme/Protease; Neuronal Signaling
Applications
COVID-19-immunoregulation
Field of Research
Infection
Assay Protocol
https://www.medchemexpress.com/1-monomyristin.html
Purity
98.0
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
CCCCCCCCCCCCCC(OCC(O)CO)=O
Molecular Formula
C17H34O4
Molecular Weight
302.45
Precautions
H302, H315, H319, H335
References & 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.|[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.|[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
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Natural Products
Clinical Information
No Development Reported

Chemical Information

Glyceryl Myristate

1-monomyristoylglycerol is a 1-monoglyceride with tetradecanoyl (myristoyl) as the acyl group. It has a role as a Caenorhabditis elegans metabolite. It is a 1-monoglyceride and a tetradecanoate ester.

CAS Number589-68-4
PubChem CID79050
IUPAC Name2,3-dihydroxypropyl tetradecanoate
Molecular FormulaC17H34O4
Molecular Weight302.4
XLogP5.2
Topological Polar Surface Area66.8
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count16
Heavy Atom Count21
Formal Charge0
Complexity231
SMILES
CCCCCCCCCCCCCC(=O)OCC(CO)O
InChI
InChI=1S/C17H34O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-17(20)21-15-16(19)14-18/h16,18-19H,2-15H2,1H3
InChIKey
DCBSHORRWZKAKO-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of Glyceryl Myristate
CAS: 589-68-4
CID: 79050
Formula: C17H34O4
MW: 302.4
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight302.4
XLogP35.2
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count16
Exact Mass302.24570956
Monoisotopic Mass302.24570956
Topological Polar Surface Area66.8 Ų
Heavy Atom Count21
Formal Charge0
Complexity231
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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