2D Structure

3D Structure

Ethyl Palmitate


Properties
PID PID00111
Mol. Weight 284.484 g/mol
LogP 6.76
Water solubility 0.000000195 mol/L at 20 °C
Hydrogen Bond Donor 0
Hydrogen Bond Acceptor 2
Rotatable Bonds 16
XLogP3 7.8

Ethyl Palmitate

Identifiers
Formula C18H36O2
PubChem CID 12366
FEMA 2451
Flavor Profile Faint wax, Fruit and butter aromas
Smiles CCCCCCCCCCCCCCCC(=O)OCC
InChl Key XIRNKXNNONJFQO-UHFFFAOYSA-N
InChl InChI=1S/C18H36O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20-4-2/h3-17H2,1-2H3
CAS Registry Number 628-97-7
IUPAC Systematic Name ethyl hexadecanoate

Organ Location Map/System Distribution of Pungent Flavor Compounds’ Targets


Note: Known Targets (Gene) from 6952 literatures, DrugBank (http://www.drugbank.ca/), STITCH (http://stitch.embl.de/), ChEMBL (https://www.ebi.ac.uk/chembl/), Therapeutic Target Database (http://bidd.nus.edu.sg/group/ttd/), and Comparative Toxicogenomics Database (CTD, http://ctdbase.org/)


Related Pungent TCM

English Name Pinyin Name (Chinese Name) Latin Name Properties in TCM merdians View Graph
Chuanxiong (Wallich Ligusticum) Equivalent plantChuan Xiong (川芎)Ligusticum chuanxiong HortWarm, PungentLiver, Gallbladder, Pericardium or Xin BaoView Graph
Odoriferous RosewoodJiang Xiang(降香)Dalbergiae Odoriferae LignumWarm,PungentSpleen, LiverView Graph

Pharmacological action

Ethyl palmitate has the effect of acaricidal activity, autoantibody. It is also Used as softener and lubricant.



Note: Click anywhere in the blank, you can drag the whole dynamic diagram. Click on a node, you can drag his location to see it more clearly. The blue circle represents pharmacology, toxicology, or daily use. Orange hexagon represents the pungent compounds.

References

1. Bu C, Duan D, Wang Y, et al. Acaricidal activity of ethyl palmitate against Tetranychus cinnabarinus[M]//Information Technology and Agricultural Engineering. Springer, Berlin, Heidelberg, 2012: 703-712.

2. ?ebestk V, Je?kov Z. Autoantibody formation against spleen in rats chemically splenectomizedby ethyl palmitate[J]. Cellular and Molecular Life Sciences, 1976, 32(4): 519-520.