Structure Database (LMSD)

Common Name
SFE 1:0/16:0
Systematic Name
Methyl hexadecanoate
Synonyms
  • WE(1:0/16:0)
LM ID
LMFA07010470
Formula
Exact Mass
Calculate m/z
270.255881
Sum Composition
Status
Curated

Classification

Biological Context

Saturated fatty acids are synthesized by both plants and animals from acetyl coenzyme A as a form of long-term energy storage. Palmitic acid is a common 16-carbon saturated fat that represents 10-20% of the normal human dietary fat intake, and approximately 25% of the total plasma fatty acids in plasma lipoproteins.1 Saturated free fatty acids induce the expression of cyclooxygenase-2.2 Palmitic acid methyl ester (MP) is a fatty acid ester whose concentration in cells is modulated by methanol. In studies with isolated Kupffer cells, MP inhibits phagocytosis and decreases cell viability. In cells treated with lipopolysaccharide, it also decreases secretion of interleukin-10, TNF-α, nitric oxide, and prostaglandin E2. This effect is thought to occur by the inhibition of NF-κB.3

This information has been provided by Cayman Chemical

References

References

Comments
Pherobase Semiochemicals

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Insecta (#50557)
10.1246/cl.1974.1333 NEW HALOGENATED MONOTERPENES FROM DESMIA (CHONDROCOCCUS) HORNEMANNI

String Representations

InChiKey (Click to copy)
FLIACVVOZYBSBS-UHFFFAOYSA-N
InChi (Click to copy)
InChI=1S/C17H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h3-16H2,1-2H3
SMILES (Click to copy)
O=C(CCCCCCCCCCCCCCC)OC

Other Databases

KEGG ID
HMDB ID
CHEBI ID
PubChem CID
Cayman ID

Calculated Physicochemical Properties

Heavy Atoms 19
Rings 0
Aromatic Rings 0
Rotatable Bonds 15
Van der Waals Molecular Volume 317.60
Topological Polar Surface Area 26.30
Hydrogen Bond Donors 0
Hydrogen Bond Acceptors 2
logP 5.64
Molar Refractivity 82.33

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Created at
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Updated at
6th Jun 2025