Structure Database (LMSD)
Common Name
Fucoxanthinol 3-stearidonate
Systematic Name
Fucoxanthinol 3-(6Z,9Z,12Z,15Z-octadecatetraenoate)
Synonyms
- FOH-3-C18:4
- FOH18:4
No other lipid differing only in stereochemistry/bond geometry found
3D model of Fucoxanthinol 3-stearidonate
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Dreissena rostriformis bugensis
(#427924)
Bivalvia
(#6544)
Separation and identification of fatty acid esters of algal carotenoid metabolites in the freshwater mussel Dreissena bugensis, by liquid chromatography with ultraviolet/visible wavelength and mass spectrometric detectors in series.,
J Chromatogr A, 2017
J Chromatogr A, 2017
Pubmed ID:
28750733
String Representations
InChiKey (Click to copy)
JWWYLBUYULTDHA-WUYYNZCESA-N
InChi (Click to copy)
InChI=1S/C58H82O6/c1-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-37-53(61)63-50-42-55(8,9)58(57(11,43-50)64-58)44-51(60)48(5)36-30-35-46(3)32-28-27-31-45(2)33-29-34-47(4)38-39-52-54(6,7)40-49(59)41-56(52,10)62/h13-14,16-17,19-20,22-23,27-36,38,49-50,59,62H,12,15,18,21,24-26,37,40-44H2,1-11H3/b14-13-,17-16-,20-19-,23-22-,28-27+,33-29+,35-30+,45-31+,46-32+,47-34+,48-36+/t39-,49-,50-,56+,57+,58-/m0/s1
SMILES (Click to copy)
[C@@]12(CC(=O)/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=[C@@]=C3[C@@](O)(C)C[C@@H](O)CC3(C)C)O[C@]1(C)C[C@@H](OC(CCCC/C=C\C/C=C\C/C=C\C/C=C\CC)=O)CC2(C)C
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
64
Rings
3
Aromatic Rings
0
Rotatable Bonds
24
Van der Waals Molecular Volume
988.02
Topological Polar Surface Area
96.36
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
6
logP
15.47
Molar Refractivity
270.16
Admin
Created at
10th Jul 2019
Updated at
17th Jul 2019