In-Silico Structure Database (LMISSD)
Systematic Name
Fucα1-3GlcNAcβ1-3Galα1-3Galβ1-4Glcβ-Cer(d18:1/24:0)
LM ID
LMSP0505DE05
Status
Active (generated by computational methods)
Exact Mass
Calculate m/z
1484.933053
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)
RPFAQDIFHOSRJH-DHFMYVLBSA-N
InChi (Click to copy)
InChI=1S/C74H136N2O27/c1-5-7-9-11-13-15-17-19-20-21-22-23-24-25-26-28-30-32-34-36-38-40-54(83)76-48(49(82)39-37-35-33-31-29-27-18-16-14-12-10-8-6-2)45-94-71-63(91)61(89)66(53(44-80)99-71)100-73-65(93)69(59(87)52(43-79)97-73)103-74-64(92)68(58(86)51(42-78)98-74)102-70-55(75-47(4)81)67(57(85)50(41-77)96-70)101-72-62(90)60(88)56(84)46(3)95-72/h37,39,46,48-53,55-74,77-80,82,84-93H,5-36,38,40-45H2,1-4H3,(H,75,81)(H,76,83)/b39-37+/t46?,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?/m0/s1
SMILES (Click to copy)
CC(=O)NC1[C@@H](O[C@H]2OC(C)[C@@H](O)C(O)[C@@H]2O)[C@H](O)C(CO)O[C@H]1O[C@@H]1C(O)[C@@H](O[C@H]2[C@@H](O)C(CO)O[C@@H](O[C@H]3[C@H](O)C(O)[C@H](OC[C@H](NC(=O)CCCCCCCCCCCCCCCCCCCCCCC)[C@H](O)/C=C/CCCCCCCCCCCCC)OC3CO)C2O)OC(CO)[C@@H]1O
References
Calculated Physicochemical Properties
Heavy Atoms
103
Rings
5
Aromatic Rings
0
Rotatable Bonds
53
Van der Waals Molecular Volume
1478.37
Topological Polar Surface Area
464.30
Hydrogen Bond Donors
17
Hydrogen Bond Acceptors
27
logP
12.13
Molar Refractivity
392.12