Structure Database (LMSD)

Common Name
MGDG(14:0/16:1(9Z))
Systematic Name
1-tetradecanoyl-2-(9Z-hexadecenoyl)-3-O-β-D-galactosyl-sn-glycerol
Synonyms
  • Monogalactosyldiacylglycerol(14:0/16:1)
LM ID
LMGL05010050
Status
Active
Exact Mass
Calculate m/z
700.51255
Formula
Abbrev


Download as...
MDLMOL SDF CSV TSV
MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".

Main

Classification

String Representations

InChiKey (Click to copy)
ARSRHYUCIPAFEB-JYKGBUINSA-N
InChi (Click to copy)
InChI=1S/C39H72O10/c1-3-5-7-9-11-13-15-16-18-20-22-24-26-28-35(42)48-32(31-47-39-38(45)37(44)36(43)33(29-40)49-39)30-46-34(41)27-25-23-21-19-17-14-12-10-8-6-4-2/h13,15,32-33,36-40,43-45H,3-12,14,16-31H2,1-2H3/b15-13-/t32-,33-,36+,37+,38-,39-/m1/s1
SMILES (Click to copy)
O([C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1)C[C@@](OC(CCCCCCC/C=C\CCCCCC)=O)([H])COC(CCCCCCCCCCCCC)=O

References

Reference
Isolation of the molecular species of monogalactosyldiacylglycerols from brown edible seaweed Sargassum horneri and their inhibitory effects on triglyceride accumulation in 3T3-L1 adipocytes
J Agric Food Chem. 2014
DOI: 10.1021/jf503068n
PMID: 25363514

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Sargassum horneri (#74089)
Phaeophyceae (#2870)
Isolation of the molecular species of monogalactosyldiacylglycerols from brown edible seaweed Sargassum horneri and their inhibitory effects on triglyceride accumulation in 3T3-L1 adipocytes.,
J Agric Food Chem, 2014
Pubmed ID: 25363514

Calculated Physicochemical Properties

Heavy Atoms 49
Rings 1
Aromatic Rings 0
Rotatable Bonds 34
Van der Waals Molecular Volume 750.88
Topological Polar Surface Area 154.05
Hydrogen Bond Donors 4
Hydrogen Bond Acceptors 10
logP 9.79
Molar Refractivity 196.40

Admin

Created at
14th Aug 2020
Updated at
14th Aug 2020
LIPID MAPS® abbreviations for glycerolipids (GL)

The LIPID MAPS® glycerolipid abbreviations (MG,DG,TG) are used here to refer to species with one, two or three radyl side-chains, respectively, where the structures of the side chains are indicated within parentheses in the 'Prefix(sn1/sn2/sn3)' format (e.g. TG(16:0/18:1(9Z)/18:0). Acyl chains are assumed by default. The alkyl ether linkage is represented by the 'O-' prefix, e.g. DG(O-16:0/18:1(9Z)/0:0), whereas the 1Z-alkenyl ether (Plasmalogen) linkage is represented by the 'P-' prefix, e.g. and DG(P-14:0/18:1(9Z)/0:0).

For Diradylglycerols and Triradylglycerols, it is not always possible to experimentally determine the exact position of radyl groups on the glycerol group. For Diradylglycerols with two different radyl groups, two different structural isomers exist. For Triradylglycerols with three different radyl groups, six different isomers exist.

Instead of drawing all possible structural isomers explicitly for Diradylglycerols and Triradylglycerols, the LIPID MAPS® abbreviation scheme supports the isomeric specification. A suffix containing 'iso' along with the number of possible isomers is appended to the abbreviation (e.g. [iso2],[iso6]) and a single unique LM_ID is assigned. The structure assigned to the LM_ID corresponds to the radyl substitution shown in the abbreviation. An option is provided to display the other isomers in the group.

The [rac] designation refers to racemic mixtures due to substitution at the sn1 and sn3 positions of glycerol.