In-Silico Structure Database (LMISSD)
Systematic Name
GlcNAcα1-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ-Cer(d18:1/24:1(15Z))
LM ID
LMSP0505CE07
Status
Active (generated by computational methods)
Exact Mass
Calculate m/z
1539.938867
Formula
Main
Classification
Category
Main Class
Sub Class
Sphingolipids [SP]
Neutral glycosphingolipids [SP05]
Galbeta1-4GlcNAcbeta1-3Galbeta1-4Glc- (Neolacto series) [SP0505]
String Representations
InChiKey (Click to copy)
RZGRCWMWLQGYBN-CYWXTRRFSA-N
InChi (Click to copy)
InChI=1S/C76H137N3O28/c1-5-7-9-11-13-15-17-19-20-21-22-23-24-25-26-28-30-32-34-36-38-40-56(88)79-49(50(87)39-37-35-33-31-29-27-18-16-14-12-10-8-6-2)46-98-74-65(95)64(94)69(55(45-84)103-74)105-76-67(97)71(61(91)53(43-82)101-76)107-73-58(78-48(4)86)63(93)68(54(44-83)102-73)104-75-66(96)70(60(90)52(42-81)100-75)106-72-57(77-47(3)85)62(92)59(89)51(41-80)99-72/h19-20,37,39,49-55,57-76,80-84,87,89-97H,5-18,21-36,38,40-46H2,1-4H3,(H,77,85)(H,78,86)(H,79,88)/b20-19-,39-37+/t49-,50+,51?,52?,53?,54?,55?,57?,58?,59+,60-,61-,62+,63+,64+,65?,66?,67?,68+,69+,70-,71-,72?,73-,74+,75-,76-/m0/s1
SMILES (Click to copy)
CC(=O)NC1[C@@H](OC(CO)[C@@H](O[C@@H]2OC(CO)[C@H](O)[C@H](O[C@H]3OC(CO)[C@@H](O)[C@H](O)C3NC(C)=O)C2O)[C@@H]1O)O[C@H]1[C@@H](O)C(CO)O[C@@H](O[C@@H]2C(CO)O[C@@H](OC[C@H](NC(=O)CCCCCCCCCCCCC/C=C\CCCCCCCC)[C@H](O)/C=C/CCCCCCCCCCCCC)C(O)[C@H]2O)C1O
References
Calculated Physicochemical Properties
Heavy Atoms
107
Rings
5
Aromatic Rings
0
Rotatable Bonds
54
Van der Waals Molecular Volume
1527.48
Topological Polar Surface Area
493.40
Hydrogen Bond Donors
18
Hydrogen Bond Acceptors
28
logP
11.31
Molar Refractivity
405.52