Structure Database (LMSD)
Systematic Name
Galα1-3(Fucα1-2)Galβ1-3GalNAcβ1-4(NeuAcα2-3)Galβ1-4Glcβ-Cer(d18:1/22:0)
Synonyms
LM ID
LMSP0601CY04
Formula
Exact Mass
Calculate m/z
1910.049997
Sum Composition
Status
Computationally Generated
3D model of
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
Biological Context
String Representations
InChiKey (Click to copy)
JIQYIANVRWTJBD-LHCJOQKLSA-N
InChi (Click to copy)
InChI=1S/C89H159N3O40/c1-6-8-10-12-14-16-18-20-21-22-23-24-25-27-29-31-33-35-37-39-60(104)92-51(52(101)38-36-34-32-30-28-26-19-17-15-13-11-9-7-2)47-119-83-73(115)70(112)75(58(45-97)124-83)126-86-74(116)80(132-89(88(117)118)40-53(102)61(90-49(4)99)78(131-89)64(106)54(103)41-93)76(59(46-98)125-86)127-82-62(91-50(5)100)77(66(108)56(43-95)121-82)128-87-81(130-84-71(113)68(110)63(105)48(3)120-84)79(67(109)57(44-96)123-87)129-85-72(114)69(111)65(107)55(42-94)122-85/h36,38,48,51-59,61-87,93-98,101-103,105-116H,6-35,37,39-47H2,1-5H3,(H,90,99)(H,91,100)(H,92,104)(H,117,118)/b38-36+/t48-,51+,52-,53+,54-,55-,56-,57-,58-,59-,61-,62-,63-,64-,65+,66+,67+,68-,69+,70-,71+,72-,73-,74-,75-,76+,77-,78-,79+,80-,81-,82+,83-,84-,85-,86+,87+,89+/m1/s1
SMILES (Click to copy)
[C@](CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[C@@H]3O[C@H](CO)[C@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[C@H]5O[C@H](CO)[C@H](O)[C@H](O)[C@H]5O)[C@H]4O[C@H]4O[C@H](C)[C@@H](O)[C@@H](O)[C@@H]4O)[C@H]3NC(=O)C)[C@H](O[C@]3(O[C@@]([H])([C@H](O)[C@H](O)CO)[C@H](NC(=O)C)[C@@H](O)C3)C(O)=O)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
132
Rings
7
Aromatic Rings
0
Rotatable Bonds
61
Van der Waals Molecular Volume
1833.14
Topological Polar Surface Area
693.14
Hydrogen Bond Donors
25
Hydrogen Bond Acceptors
40
logP
10.07
Molar Refractivity
483.56
Admin
Created at
-
Updated at
21st Jul 2021