Structure Database (LMSD)

OH OH HO HO O O OH NH HO O OH O O NH HO HO HO HO OH O O O O O OH O HO O HO HO NH H OH O NH H OH HO O O OH OH O O O
Common Name
GD1b(d18:1/22:0)
Systematic Name
Galβ1-3GalNAcβ1-4(NeuAcα2-8NeuAcα2-3)Galβ1-4Glcβ-Cer(d18:1/22:0)
Synonyms
LM ID
LMSP0601AQ04
Formula
Exact Mass
Calculate m/z
1893.034681
Sum Composition
Status
Active (generated by computational methods)

Main

Classification

String Representations

InChiKey (Click to copy)
AUWZNXKYUYRHNS-RCJDSYPVSA-N
InChi (Click to copy)
InChI=1S/C88H156N4O39/c1-6-8-10-12-14-16-18-20-21-22-23-24-25-27-29-31-33-35-37-39-62(106)92-52(53(102)38-36-34-32-30-28-26-19-17-15-13-11-9-7-2)48-120-82-73(114)71(112)75(60(46-97)123-82)125-84-74(115)80(76(61(47-98)124-84)126-81-65(91-51(5)101)77(68(109)58(44-95)121-81)127-83-72(113)70(111)67(108)57(43-94)122-83)131-88(86(118)119)41-55(104)64(90-50(4)100)79(130-88)69(110)59(45-96)128-87(85(116)117)40-54(103)63(89-49(3)99)78(129-87)66(107)56(105)42-93/h36,38,52-61,63-84,93-98,102-105,107-115H,6-35,37,39-48H2,1-5H3,(H,89,99)(H,90,100)(H,91,101)(H,92,106)(H,116,117)(H,118,119)/b38-36+/t52-,53+,54-,55-,56+,57+,58+,59+,60+,61+,63+,64+,65+,66+,67-,68-,69+,70-,71+,72+,73+,74+,75+,76-,77+,78+,79+,80+,81-,82+,83-,84-,87+,88-/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](O[C@@H]3O[C@@H]([C@@H]([C@@H]([C@H]3NC(C)=O)O[C@H]3[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O3)O)CO)[C@H](O[C@]3(O[C@@]([H])([C@H](O)[C@H](O[C@]4(O[C@@]([H])([C@H](O)[C@H](O)CO)[C@H](NC(=O)C)[C@@H](O)C4)C(O)=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

References

Other Databases

PubChem CID
SwissLipids ID

Calculated Physicochemical Properties

Heavy Atoms 131
Rings 6
Aromatic Rings 0
Rotatable Bonds 63
Van der Waals Molecular Volume 1825.13
Topological Polar Surface Area 698.55
Hydrogen Bond Donors 25
Hydrogen Bond Acceptors 43
logP 9.42
Molar Refractivity 479.09

Reactions

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Reactions graph legend

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Created at
-
Updated at
26th Aug 2021