Skip to Content
Merck
All Photos(2)

Key Documents

G9287

Sigma-Aldrich

Globotriose

Synonym(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

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C18H32O16
CAS Number:
66580-68-5
Molecular Weight:
504.44
MDL number:
MFCD01076415
UNSPSC Code:
12352201
PubChem Substance ID:
329799986
Pricing and availability is not currently available.

Assay

≥95% (HPLC)

Quality Level

200

form

powder

storage temp.

2-8°C

SMILES string

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

InChI key

FYGDTMLNYKFZSV-ANKSBSNASA-N

Other Notes

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SLBT5524
SLBL3967V
SLBK6410V
SLBF1813V
SLBC9581V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H C Hansen et al.
Carbohydrate research, 307(3-4), 243-251 (1998-07-24)
Derivatives of galabiose (alpha-D-Galp-(1-->4)-D-Galp) and globotriose (a-D-Galp-(1-->4)-beta-D-Galp-(1-->4)-D-Glcp) were coupled to various 1,2- and 1,3-dihydroxymethyl- and dimercapto-methylbenzenes to give the corresponding divalent glycosides, potentially useful as inhibitors of bacterial adhesion.
H C Hansen et al.
Carbohydrate research, 322(3-4), 166-180 (2000-01-19)
Six aminodeoxy 2-(trimethylsilyl)ethyl (Me3SiEt) glycoside analogues of galabiose (4'- and 6'-aminodeoxy) and globotriose (6"-, 4"-, 2"-, and 6'-aminodeoxy) were synthesized by glycosylation of protected Me3SiEt galactoside and lactoside acceptors with azido-substituted monosaccharide donors, followed by reduction of the azido groups
Xuebing Li et al.
Journal of medicinal chemistry, 55(6), 2702-2710 (2012-03-01)
Shiga toxin (Stx)-producing Escherichia coli (STEC) causes diarrhea and colitis in humans that can develop into a life-threatening hemolytic uremic syndrome (HUS). Developing efficient means of controlling STEC diseases, for which no drugs or vaccines are currently available, remains a
Hirofumi Dohi et al.
Carbohydrate research, 337(11), 983-989 (2002-06-01)
New thioglycosyl donors (o-methoxycarbonylphenyl 2,3,4,6-tetra-O-benzyl-1-thio-beta-D-galactopyranoside and its 6-O-acetyl analogue) were designed and used for the synthesis of glycoconjugate polymers carrying Gb(3) [Gal(alpha1-->4)Gal(beta1-->4)Glc] and isoGb(3) [Gal(alpha1-->3)Gal(beta1-->4)Glc] clusters as side chains. These donors scarcely evolved the unpleasant odor of thiophenols and showed
James L Leach et al.
Antimicrobial agents and chemotherapy, 49(9), 3842-3846 (2005-08-30)
Epithelial cells lining the urinary tract are rich in globo series glycolipids, structurally defined by a Galalpha1,4Gal motif in the oligosaccharide moiety of this glycolipid family. This Galalpha1,4Gal motif is the attachment target for the P-fimbrial adhesin of uropathogenic Escherichia
View All Related Papers

Articles

Review of O-Linked Glycoproteins

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service