66580-68-5

Basic information

• Product Name: GLOBOTRIOSE
• Synonyms: ALPHA-D-GAL-[1->4]-BETA-D-GAL-[1->4]-D-GLC;4-O-(4-O-ALPHA-D-GALACTOPYRANOSYL-BETA-D-GALACTOPYRANOSYL)-D-GLUCOPYRANOSE;GLOBOTRIOSE;GAL-ALPHA1-4GAL-BETA1-4GLC;4-O-(4-O-A-D-GALACTOPYRANOSYL-B-D-*GALAC TOPYRANOSYL;α-d-gal-(1→4)-β-d-gal-(1→4)-d-glc;Globotriose ,98%;Globotriaose
• CAS NO: 66580-68-5
• Molecular Formula: C₁₈H₃₂O₁₆
• Molecular Weight: 504.44
• Mol File: 66580-68-5.mol

Chemical Properties

• Boiling Point: 968.5 °C at 760 mmHg
• Flash Point: 332.9 °C
• Appearance: /
• Density: 1.75 g/cm³
• Vapor Pressure: 6.5E-35mmHg at 25°C
• Refractive Index: 1.673
• Storage Temp.: 2-8°C
• PKA: 12.39±0.20(Predicted)
• CAS DataBase Reference: GLOBOTRIOSE(CAS DataBase Reference)
• NIST Chemistry Reference: GLOBOTRIOSE(66580-68-5)
• EPA Substance Registry System: GLOBOTRIOSE(66580-68-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 66580-68-5(Hazardous Substances Data)

Usage

Uses

Used in Cancer Research and Treatment:
Globotriose is used as a biomarker for predicting and/or detecting immune responses to cancer vaccines in patients with cancer or specifically prostate cancer. Its presence on the surface of cancer cells makes it a potential target for immune-based therapies and diagnostic tools.

InChI:InChI=1/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

Upstream product

• 57-50-1 Sucrose 
• 69-79-4 D-maltose 
• 7585-39-9 β‐cyclodextrin 

Downstream Products

• 50-99-7 D-glucose 
• 1141738-22-8 C₄₅H₆₃NO₁₉S 
• 1196681-94-3 C₄₄H₆₅N₅O₂₀ 

Relevant articles and documents

Regioselective glucosylation of inositols catalyzed by Thermoanaerobacter sp. CGTase

Monoglucosylated products of l-chiro-, d-chiro-, muco-, and allo-inositol were synthesized by regioselective α-d-glucosylation with cyclodextrin glucosyl transferase from Thermoanaerobacter sp. after hydrolysis of by products with Aspergillus niger glucoamylase. While the reactions carried out with d-chiro-, muco-, and allo-inositol resulted in the regioselective formation of monoglucosylated products, two products were obtained in the reaction with l-chiro-inositol. Through the structural characterization of the glucosylated inositols here we demonstrated that the selectivity observed in the glucosylation of several inositols by Thermoanaerobacter sp. CGTase, is analogous to the specificity observed for the glucosylation of β-d-glucopyranose and equivalent glucosides.

Branched alpha-glucan, alpha-glucosyltransferase which forms the glucan, their preparation and uses

The present invention has objects to provide a glucan useful as water-soluble dietary fiber, its preparation and uses. The present invention solves the above objects by providing a branched α-glucan, which is constructed by glucose molecules and characterized by methylation analysis as follows: (1) Ratio of 2,3,6-trimethyl-1,4,5-triacetyl-glucitol to 2,3,4-trimethyl-1,5,6-triacetyl-glucitol is in the range of 1:0.6 to 1:4;(2) Total content of 2,3,6-trimethyl-1,4,5-triacetyl-glucitol and 2,3,4-trimethyl-1,5,6-triacetyl-glucitol is 60% or higher in the partially methylated glucitol acetates;(3) Content of 2,4,6-trimethyl-1,3,5-triacetyl-glucitol is 0.5% or higher but less than 10% in the partially methylated glucitol acetates; and(4) Content of 2,4-dimethyl-1,3,5,6-tetraacetyl-glucitol is 0.5% or higher in the partially methylated glucitol acetates; a novel α-glucosyltransferase which forms the branched α-glucan, processes for producing them, and their uses.

Molecular cloning and functional expression of a new amylosucrase from Alteromonas macleodii

The presence of amylosucrase in 12 Alteromonas and Pseudoalteromonas strains was examined. Two Alteromonas species (Alteromonas addita KCTC 12195 and Alteromonas macleodii KCTC 2957) possessed genes that had high sequence homology to known amylosucrases. Genomic clones containing the ASase analogs were obtained from A. addita and A. macleodii, and the deduced amino acid sequences of the corresponding genes (aaas and amas, respectively) revealed that they were highly similar to the ASases of Neisseria polysaccharea, Deinococcus radiodurans, and Deinococcus geothermalis. Functional expression of amas in Escherichia coli was successful, and typical ASase activity was detected in purified recombinant AMAS, whereas the purified recombinant AAAS was nonfunctional. Although maximum total activity of AMAS was observed at 45 °C, the ratio of transglycosylation to total activity increased as the temperature decreased from 55 to 25 °C. These results imply that transglycosylation occurs preferentially at lower temperatures while hydrolysis is predominant at higher temperatures.

Pullulanase-Amylase Complex Enzyme from Bacillus subtilis

A novel pullulanase-amylase complex enzyme, which hydrolyzes pullulan into maltotriose as well as starch into maltose and maltotriose as the main products, was found in the culture filtrate of a strain of Bacillus subtilis newly isolated from soil.The enzyme was purified to almost complete homogeneity by means of calcium phosphate gel adsorption, DEAE-Sepharose column chromatography and Bio-gel A-1.5 m filtration.The optimum pH of the pullulanase activity was observed at around 7.0 to 7.5, with a discernible shoulder around pH 5.0.While the optimum pH of the amylase activity was 6 - 7.The optimum temperatures of the pullulanase and amylase activities were about 60 deg C and about 50 deg C, respectively.The molecular weight was estimated to be about 450,000 by the gel filtration method.The enzyme could be used for the production of glucose from starch with glucoamylase and the production of a new type of syrup containing a relatively high amount of maltotriose, 50 - 55 percent, from starch.