Structure Database (LMSD)

O OH O HO O OH OH O O HO NH OH O OH HO OH OH O HO HO O O O OH O O HO NH H OH O NH H HO O OH OH O O HO OH O
Common Name
type II H antigen(d18:1/18:0)
Systematic Name
Fucα1-2Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ-Cer(d18:1/18:0)
Synonyms
LM ID
LMSP0505AM02
Formula
Exact Mass
Calculate m/z
1765.971352
Sum Composition
Status
Active (generated by computational methods)

Main

Classification

String Representations

InChiKey (Click to copy)
DCWYXKSPMNJIRZ-ZRYHESNKSA-N
InChi (Click to copy)
InChI=1S/C82H147N3O37/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-54(95)85-46(47(94)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2)42-109-78-67(106)65(104)72(53(41-91)116-78)118-81-69(108)74(60(99)50(38-88)112-81)121-76-55(83-44(4)92)61(100)70(51(39-89)114-76)117-80-68(107)73(59(98)49(37-87)111-80)120-77-56(84-45(5)93)62(101)71(52(40-90)115-77)119-82-75(64(103)58(97)48(36-86)113-82)122-79-66(105)63(102)57(96)43(3)110-79/h32,34,43,46-53,55-82,86-91,94,96-108H,6-31,33,35-42H2,1-5H3,(H,83,92)(H,84,93)(H,85,95)/b34-32+/t43-,46+,47-,48-,49-,50-,51-,52-,53-,55-,56-,57-,58+,59+,60+,61-,62-,63-,64+,65-,66+,67-,68-,69-,70-,71-,72-,73+,74+,75-,76+,77+,78-,79-,80+,81+,82+/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](O[C@@H]3O[C@H](CO)[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]6O[C@H](CO)[C@H](O)[C@H](O)[C@H]6O[C@H]6O[C@H](C)[C@@H](O)[C@@H](O)[C@@H]6O)[C@H](O)[C@H]5NC(=O)C)[C@H]4O)[C@H](O)[C@H]3NC(=O)C)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC

References

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 122
Rings 7
Aromatic Rings 0
Rotatable Bonds 54
Van der Waals Molecular Volume 1688.31
Topological Polar Surface Area 635.61
Hydrogen Bond Donors 23
Hydrogen Bond Acceptors 37
logP 9.02
Molar Refractivity 447.38

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Created at
-
Updated at
26th Jul 2021