Structure Database (LMSD)

Common Name
1-oleoyl-2-Dihydrosterculoyl-3-O-beta-d-glucopyranosyl-(1->6)-alpha-d-galactopyranosyl-(1->2)-alpha-d-glucosyl-sn-glycerol
Systematic Name
1-(9Z-octadecenoyl)-2-(9,10-methylene-octadecanoic acid)-3-O-β-d-glucopyranosyl-(1->6)-α-d-galactopyranosyl-(1->2)-α-d-glucosyl-sn-glycerol
Synonyms
  • GL3
LM ID
LMGL05010069
Status
Active
Exact Mass
Calculate m/z
1120.7121
Formula


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)
GNMOEEWDWWMLIZ-XHTAHCMQSA-N
InChi (Click to copy)
InChI=1S/C58H104O20/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-23-27-31-45(61)71-36-41(74-46(62)32-28-24-20-22-26-30-40-33-39(40)29-25-21-10-8-6-4-2)37-72-58-55(52(68)48(64)43(35-60)76-58)78-57-54(70)51(67)49(65)44(77-57)38-73-56-53(69)50(66)47(63)42(34-59)75-56/h14-15,39-44,47-60,63-70H,3-13,16-38H2,1-2H3/b15-14-/t39?,40?,41-,42-,43-,44-,47-,48-,49+,50+,51+,52+,53-,54-,55-,56-,57-,58+/m1/s1
SMILES (Click to copy)
O([C@@H]1[C@H](O[C@@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)O2)[C@@H](O)[C@H](O)[C@@H](CO)O1)C[C@]([H])(OC(CCCCCCCC1CC1CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Lactiplantibacillus plantarum (#1590)
Bacilli (#91061)
Isolation and structural characterisation of the major glycolipids from Lactobacillus plantarum.,
Carbohydr Res, 2012
Pubmed ID: 22683117

Calculated Physicochemical Properties

Heavy Atoms 78
Rings 4
Aromatic Rings
Rotatable Bonds 45
Van der Waals Molecular Volume 1130.40
Topological Polar Surface Area 316.49
Hydrogen Bond Donors 10
Hydrogen Bond Acceptors 20
logP 11.07
Molar Refractivity 297.83

Admin

Created at
25th Jan 2022
Updated at
25th Jan 2022
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.