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Details

Stereochemistry ABSOLUTE
Molecular Formula C73H130N3O31.Na
Molecular Weight 1568.8046
Optical Activity UNSPECIFIED
Defined Stereocenters 28 / 28
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of GANGLIOSIDE GM1 SODIUM (D18:1/18:0)

SMILES

[Na+].[H][C@@]5(O[C@H]1[C@@H](O)[C@@H](CO)O[C@@]([H])(O[C@H]2[C@@H](CO)O[C@@]([H])(O[C@@H]3[C@@H](CO)O[C@@H](OC[C@H](NC(=O)CCCCCCCCCCCCCCCCC)[C@H](O)\C=C\CCCCCCCCCCCCC)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[C@@]4(C[C@H](O)[C@@H](NC(C)=O)[C@@]([H])(O4)[C@H](O)[C@H](O)CO)C([O-])=O)[C@@H]1NC(C)=O)O[C@H](CO)[C@H](O)[C@H](O)[C@H]5O

InChI

InChIKey=LFNNYGUBFYVSKX-POYTVKKJSA-M
InChI=1S/C73H131N3O31.Na/c1-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-52(87)76-44(45(84)33-31-29-27-25-23-21-18-16-14-12-10-8-6-2)41-98-69-61(94)59(92)63(50(39-80)101-69)103-71-62(95)67(107-73(72(96)97)35-46(85)53(74-42(3)82)66(106-73)55(88)47(86)36-77)64(51(40-81)102-71)104-68-54(75-43(4)83)65(57(90)49(38-79)99-68)105-70-60(93)58(91)56(89)48(37-78)100-70;/h31,33,44-51,53-71,77-81,84-86,88-95H,5-30,32,34-41H2,1-4H3,(H,74,82)(H,75,83)(H,76,87)(H,96,97);/q;+1/p-1/b33-31+;/t44-,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-,73-;/m0./s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C73H130N3O31
Molecular Weight 1545.8148
Charge -1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 28 / 28
E/Z Centers 1
Optical Activity UNSPECIFIED

Ganglioside GM1 is a monosialo-glycosphingolipid belonging to the gangliotetrahexosyl series that abundant in neurons of all animal species and plays important roles in many cell physiological processes, including differentiation, memory control, cell signaling, neuronal protection, neuronal recovery, and apoptosis. Ganglioside GM1 in neurons helps to transfer information from the exterior to the interior of the cell, through specific recognition and binding of biologically active molecules (membrane receptors and ion channels), and has specific functions in nerve conduction and/or synaptic transmission. The mechanisms underlying the effects of Ganglioside GM1 remain unclear in many cases, but it appears that these effects are often due to specific interactions between Ganglioside GM1 and proteins involved in signaling processes, within Ganglioside GM1-enriched lipid rafts in the plasma membrane. Ganglioside GM1 is a major component of total ganglioside mixtures from mammalian brains, from which it can be extracted and purified in large amounts. Ganglioside GM1 was widely used in the past as a therapeutic drug for a wide variety of neurological disorders. Further studies have shown that Ganglioside GM1 has immunogenic properties and led to the production of antibodies that promoted peripheral neuropathies such as Guillain–Barré syndrome.

CNS Activity

Curator's Comment: Gangliosides are abundant in neurons of all animal species

Approval Year

PubMed

PubMed

TitleDatePubMed
Neurochemical changes on oxidative stress in rat hippocampus during acute phase of pilocarpine-induced seizures.
2010 Jan
Neurophysiological and immunohistochemical studies of IgG anti-GM1 monoclonal antibody on neuromuscular transmission: effects in rat neuromuscular junctions.
2014 Feb
Methylmercury causes neuronal cell death through the suppression of the TrkA pathway: in vitro and in vivo effects of TrkA pathway activators.
2015 Feb 1
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:09:47 GMT 2023
Edited
by admin
on Sat Dec 16 16:09:47 GMT 2023
Record UNII
JU7UPN50YT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GANGLIOSIDE GM1 SODIUM (D18:1/18:0)
Common Name English
OCTADECANAMIDE, N-((1S,2R,3E)-1-(((O-.BETA.-D-GALACTOPYRANOSYL-(1->3)-O-2-(ACETYLAMINO)-2-DEOXY-.BETA.-D-GALACTOPYRANOSYL-(1->4)-O-(N-ACETYL-.ALPHA.-NEURAMINOSYL-(2->3))-O-.BETA.-D-GALACTOPYRANOSYL-(1->4)-.BETA.-D-GLUCOPYRANOSYL)OXY)METHYL)-2-HYDROXY-3-H
Systematic Name English
Code System Code Type Description
FDA UNII
JU7UPN50YT
Created by admin on Sat Dec 16 16:09:48 GMT 2023 , Edited by admin on Sat Dec 16 16:09:48 GMT 2023
PRIMARY
CAS
1694670-82-0
Created by admin on Sat Dec 16 16:09:48 GMT 2023 , Edited by admin on Sat Dec 16 16:09:48 GMT 2023
PRIMARY
PUBCHEM
146675098
Created by admin on Sat Dec 16 16:09:48 GMT 2023 , Edited by admin on Sat Dec 16 16:09:48 GMT 2023
PRIMARY
SMS_ID
100000166814
Created by admin on Sat Dec 16 16:09:48 GMT 2023 , Edited by admin on Sat Dec 16 16:09:48 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE