N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt)

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N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt) Basic information
Product Name:N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt)
Synonyms:N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt);C18 Ganglioside GM3-d3 (d18:1/18:0-d3) (ammonium salt, synthetic)
CAS:2692623-85-9
MF:
MW:0
EINECS:
Product Categories:
Mol File:Mol File
N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt) Structure
N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt) Chemical Properties
solubility Chloroform:
Methanol: (2:1): Soluble
Safety Information
MSDS Information
N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt) Usage And Synthesis
UsesGanglioside GM3-d3 ammonium is a deuterated labeled Ganglioside GM3 ammonium[1].
References[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110
[2] PURNA MUKHERJEE. Thematic review series: sphingolipids. Ganglioside GM3 suppresses the proangiogenic effects of vascular endothelial growth factor and ganglioside GD1a.[J]. Journal of Lipid Research, 2008: 929-938. DOI: 10.1194/jlr.r800006-jlr200
[3] THOMAS N SEYFRIED  Purna M. Ganglioside GM3 Is Antiangiogenic in Malignant Brain Cancer.[J]. Journal of Oncology, 2010: 961243. DOI: 10.1155/2010/961243
[4] KAZUYA KABAYAMA. Dissociation of the insulin receptor and caveolin-1 complex by ganglioside GM3 in the state of insulin resistance.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2007, 104 34: 13678-13683. DOI: 10.1073/pnas.0703650104
N-oMega-CD3-Octadecanoyl-Monosialoganglioside GM3 (NH4-salt) Preparation Products And Raw materials
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