In-Silico Structure Database (LMISSD)
Systematic Name
Galβ1-4GlcNAcβ1-6GalNAcβ1-3Galα1-4Galβ1-4Glcβ-Cer(d18:1/24:0)
LM ID
LMSP0502BG05
Status
Active (generated by computational methods)
Exact Mass
Calculate m/z
1704.007342
Formula
Main
Classification
Category
Main Class
Sub Class
Sphingolipids [SP]
Neutral glycosphingolipids [SP05]
Galalpha1-4Galbeta1-4Glc- (Globo series) [SP0502]
String Representations
InChiKey (Click to copy)
XBBFOSVUGDUTAQ-WLORUCETSA-N
InChi (Click to copy)
InChI=1S/C82H149N3O33/c1-5-7-9-11-13-15-17-19-20-21-22-23-24-25-26-28-30-32-34-36-38-40-58(94)85-50(51(93)39-37-35-33-31-29-27-18-16-14-12-10-8-6-2)46-107-79-70(104)67(101)74(55(44-89)112-79)116-81-71(105)68(102)75(56(45-90)113-81)117-82-72(106)76(63(97)53(42-87)110-82)118-78-59(83-48(3)91)64(98)62(96)57(114-78)47-108-77-60(84-49(4)92)65(99)73(54(43-88)111-77)115-80-69(103)66(100)61(95)52(41-86)109-80/h37,39,50-57,59-82,86-90,93,95-106H,5-36,38,40-47H2,1-4H3,(H,83,91)(H,84,92)(H,85,94)/b39-37+/t50-,51+,52?,53?,54?,55?,56?,57?,59?,60?,61-,62-,63-,64+,65+,66-,67+,68+,69?,70?,71?,72?,73+,74+,75-,76-,77+,78-,79+,80-,81-,82?/m0/s1
SMILES (Click to copy)
CC(=O)NC1[C@@H](OC(CO[C@@H]2OC(CO)[C@@H](O[C@@H]3OC(CO)[C@H](O)[C@H](O)C3O)[C@H](O)C2NC(C)=O)[C@H](O)[C@@H]1O)O[C@@H]1C(O)[C@H](O[C@H]2C(CO)O[C@@H](O[C@@H]3C(CO)O[C@@H](OC[C@H](NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)[C@H](O)/C=C/CCCCCCCCCCCCC)C(O)[C@H]3O)C(O)[C@H]2O)OC(CO)[C@@H]1O
References
Calculated Physicochemical Properties
Heavy Atoms
118
Rings
6
Aromatic Rings
0
Rotatable Bonds
58
Van der Waals Molecular Volume
1665.51
Topological Polar Surface Area
574.62
Hydrogen Bond Donors
21
Hydrogen Bond Acceptors
33
logP
11.07
Molar Refractivity
441.30