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Principaux documents

G9287

Sigma-Aldrich

Globotriose

Synonyme(s) :

α-D-Gal-(1→4)-β-D-Gal-(1→4)-D-Glc, 4-O-(4-O-α-D-Galactopyranosyl-β-D-galactopyranosyl)-D-glucopyranose

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About This Item

Formule empirique (notation de Hill):
C18H32O16
Numéro CAS:
Poids moléculaire :
504.44
Numéro MDL:
Code UNSPSC :
12352201
ID de substance PubChem :

Essai

≥95% (HPLC)

Niveau de qualité

Forme

powder

Température de stockage

2-8°C

Chaîne SMILES 

OC[C@H]1O[C@H](O[C@@H]2[C@H](O)[C@@H](O)[C@@H](O[C@@H]2CO)O[C@H]3[C@H](O)[C@@H](O)C(O)O[C@@H]3CO)[C@H](O)[C@@H](O)[C@H]1O

InChI

1S/C18H32O16/c19-1-4-7(22)8(23)12(27)17(31-4)34-15-6(3-21)32-18(13(28)10(15)25)33-14-5(2-20)30-16(29)11(26)9(14)24/h4-29H,1-3H2/t4-,5-,6-,7+,8+,9-,10-,11-,12-,13-,14-,15+,16?,17-,18+/m1/s1

Clé InChI

FYGDTMLNYKFZSV-ANKSBSNASA-N

Autres remarques

To gain a comprehensive understanding of our extensive range of Oligosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Consulter la Bibliothèque de documents

S Haataja et al.
Glycoconjugate journal, 16(1), 67-71 (1999-12-02)
Streptococcus suis causes meningitis and other serious infections in pigs and humans, and binds to host cell globotriosylceramide. In order to determine the essential hydroxyls involved in binding, the complete set of monodeoxy derivatives of the receptor trisaccharide Gal alpha1-Gal
Jianbo Zhang et al.
Organic & biomolecular chemistry, 1(17), 3048-3053 (2003-10-02)
The carbohydrate chains decorating cell membranes and secreted proteins participate in a range of important biological processes. However, their ultimate significance and possible therapeutic potential have not been fully explored due to the lack of economical methods for their production.
Eva Blomberg et al.
Langmuir : the ACS journal of surfaces and colloids, 22(24), 10038-10046 (2006-11-17)
A set of oligo(ethylene glycol)-terminated and globotriose-terminated self-assembled monolayers (SAMs) has been prepared on gold substrates. Such model surfaces are well defined and have good stability due to the strong binding of thiols and disulfides to the gold substrate. They
Yuh-Yih Chien et al.
Chembiochem : a European journal of chemical biology, 9(7), 1100-1109 (2008-04-10)
Compared to monovalent carbohydrates, multivalent carbohydrate ligands exhibit significantly enhanced binding affinities to their interacting proteins. Here, we report globotriose (P(k) ligand)-functionalized gold nanoparticle (AuNP) probes for the investigation of multivalent interactions with the B(5) subunit of Shiga-like toxin I
P I Kitov et al.
Carbohydrate research, 307(3-4), 361-369 (1998-07-24)
The Pk trisaccharide and the central disaccharide element of asialo GM1 activated as their trichloroacetimidates were each used to glycosylate 16-(p-toluensulfonyloxy) hexadecanol 1. Displacement of the tosyl group by thiocyanate followed by sodium borohydride reduction and saponification afforded oligosaccharide 16-mercaptohexadecanyl

Articles

O-Linked glycoproteins are usually large proteins with a molecular mass of >200 kDa. Glycosylation generally occurs in high-density clusters and may represent as much as 50-80% of the overall mass.

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