Structure Database (LMSD)

Common Name
type II H antigen(d18:1/16:0)
Systematic Name
Fucα1-2Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ-Cer(d18:1/16:0)
Synonyms
LM ID
LMSP0505AM01
Formula
Exact Mass
Calculate m/z
1737.940052
Sum Composition
Status
Active (generated by computational methods)

Classification

String Representations

InChiKey (Click to copy)
LJALWCRNCSAMGP-QSYXHWFLSA-N
InChi (Click to copy)
InChI=1S/C80H143N3O37/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-45(92)44(83-52(93)33-31-29-27-25-23-21-19-17-15-13-11-9-7-2)40-107-76-65(104)63(102)70(51(39-89)114-76)116-79-67(106)72(58(97)48(36-86)110-79)119-74-53(81-42(4)90)59(98)68(49(37-87)112-74)115-78-66(105)71(57(96)47(35-85)109-78)118-75-54(82-43(5)91)60(99)69(50(38-88)113-75)117-80-73(62(101)56(95)46(34-84)111-80)120-77-64(103)61(100)55(94)41(3)108-77/h30,32,41,44-51,53-80,84-89,92,94-106H,6-29,31,33-40H2,1-5H3,(H,81,90)(H,82,91)(H,83,93)/b32-30+/t41-,44+,45-,46-,47-,48-,49-,50-,51-,53-,54-,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+/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(CCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 120
Rings 7
Aromatic Rings 0
Rotatable Bonds 52
Van der Waals Molecular Volume 1653.71
Topological Polar Surface Area 635.61
Hydrogen Bond Donors 23
Hydrogen Bond Acceptors 37
logP 8.24
Molar Refractivity 438.15

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Created at
-
Updated at
26th Jul 2021