Structure Database (LMSD)
Systematic Name
Galα1-3(GlcNAcβ1-6)Galβ1-4Glcβ-Cer(d18:1/22:0)
Synonyms
LM ID
LMSP0506AP04
Formula
Exact Mass
Calculate m/z
1310.843843
Sum Composition
Status
Active (generated by computational methods)
No other lipid differing only in stereochemistry/bond geometry found
3D model of
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Main
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
KSZIQQRDMVNYEF-PJLKLQCISA-N
InChi (Click to copy)
InChI=1S/C66H122N2O23/c1-4-6-8-10-12-14-16-18-19-20-21-22-23-25-27-29-31-33-35-37-50(74)68-44(45(73)36-34-32-30-28-26-24-17-15-13-11-9-7-5-2)41-84-64-59(82)57(80)61(48(40-71)88-64)90-66-60(83)62(91-65-58(81)56(79)53(76)47(39-70)87-65)54(77)49(89-66)42-85-63-51(67-43(3)72)55(78)52(75)46(38-69)86-63/h34,36,44-49,51-66,69-71,73,75-83H,4-33,35,37-42H2,1-3H3,(H,67,72)(H,68,74)/b36-34+/t44-,45+,46+,47+,48+,49+,51+,52+,53-,54-,55+,56-,57+,58+,59+,60+,61+,62-,63+,64+,65+,66-/m0/s1
SMILES (Click to copy)
[C@](CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3NC(=O)C)[C@H](O)[C@H](O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC
References
Calculated Physicochemical Properties
Heavy Atoms
91
Rings
4
Aromatic Rings
0
Rotatable Bonds
49
Van der Waals Molecular Volume
1317.17
Topological Polar Surface Area
403.31
Hydrogen Bond Donors
15
Hydrogen Bond Acceptors
23
logP
11.07
Molar Refractivity
349.10
Admin
Created at
-
Updated at
26th Jul 2021