Structure Database (LMSD)

OH O H NH O O OH H OH HO OH OH
Common Name
GlcCer(d14:1(4E)/20:0(2OH))
Systematic Name
N-(2-hydroxy-eicosanoyl)-1-β-glucosyl-tetradecasphing-4-enine
Synonyms
LM ID
LMSP0501AA65
Formula
Exact Mass
Calculate m/z
715.559834
Sum Composition
Abbrev Chains
GlcCer 14:1;O2/20:0;O
Status
Active

Main

Classification

String Representations

InChiKey (Click to copy)
YYILQTLJZBSOCA-QBZFBHFLSA-N
InChi (Click to copy)
InChI=1S/C40H77NO9/c1-3-5-7-9-11-13-14-15-16-17-18-19-21-23-25-27-29-34(44)39(48)41-32(33(43)28-26-24-22-20-12-10-8-6-4-2)31-49-40-38(47)37(46)36(45)35(30-42)50-40/h26,28,32-38,40,42-47H,3-25,27,29-31H2,1-2H3,(H,41,48)/b28-26+/t32-,33+,34?,35+,36+,37-,38+,40+/m0/s1
SMILES (Click to copy)
[C@](CO[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)([H])(NC(C(O)CCCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCC

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Drosophila melanogaster (#7227)
Insecta (#50557)
Biochemical membrane lipidomics during Drosophila development.,
Dev Cell, 2013
Pubmed ID: 23260625

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 50
Rings 1
Aromatic Rings 0
Rotatable Bonds 33
Van der Waals Molecular Volume 773.03
Topological Polar Surface Area 171.01
Hydrogen Bond Donors 7
Hydrogen Bond Acceptors 9
logP 9.22
Molar Refractivity 204.65

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Created at
-
Updated at
26th Jul 2021