Structure Database (LMSD)

Common Name
SSEA-3 antigen(d18:1/18:0)
Systematic Name
Galβ1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ-Cer(d18:1/18:0)
Synonyms
LM ID
LMSP0502AE02
Formula
Exact Mass
Calculate m/z
1416.834068
Sum Composition
Status
Active (generated by computational methods)

Classification

Reactions

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Reactions are shown if the E.C. number of the enzyme catalysing it is annotated in the UniProt database for a species belonging to the selected taxonomic class.
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Reactions graph legend

String Representations

InChiKey (Click to copy)
VQNDKBDQWZJESH-WEFDOZSRSA-N
InChi (Click to copy)
InChI=1S/C68H124N2O28/c1-4-6-8-10-12-14-16-18-19-21-23-25-27-29-31-33-48(78)70-41(42(77)32-30-28-26-24-22-20-17-15-13-11-9-7-5-2)39-89-65-57(86)54(83)60(46(37-74)93-65)95-67-58(87)55(84)61(47(38-75)94-67)96-68-59(88)63(52(81)45(36-73)92-68)98-64-49(69-40(3)76)62(51(80)44(35-72)90-64)97-66-56(85)53(82)50(79)43(34-71)91-66/h30,32,41-47,49-68,71-75,77,79-88H,4-29,31,33-39H2,1-3H3,(H,69,76)(H,70,78)/b32-30+/t41-,42+,43+,44+,45+,46+,47+,49+,50-,51-,52-,53-,54+,55+,56+,57+,58+,59+,60+,61-,62+,63-,64-,65+,66-,67-,68+/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](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]4NC(=O)C)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 98
Rings 5
Aromatic Rings 0
Rotatable Bonds 48
Van der Waals Molecular Volume 1383.36
Topological Polar Surface Area 484.53
Hydrogen Bond Donors 18
Hydrogen Bond Acceptors 28
logP 9.05
Molar Refractivity 366.32

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Created at
-
Updated at
26th Jul 2021