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M9672

6-O-α-Maltosyl-β-cyclodextrin hydrate

Name: 6-O-α-Maltosyl-β-cyclodextrin hydrate
Brand: SIGMA

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About This Item

Formule empirique (notation de Hill):

C₅₄H₉₀O₄₅

Numéro CAS:

104723-60-6

Poids moléculaire :

1459.27

Numéro MDL:

MFCD00678869

Code UNSPSC :

12352201

Forme

powder

Activité optique

[α]25/D 160 to 175 °, c = 0.6% (w/v) in water

Température de stockage

2-8°C

Description générale

6-O-α-Maltosyl-β-cyclodextrin hydrate forms a soluble inclusion complex with cholesterol.

Application

6-O-α-Maltosyl-β-cyclodextrin has been used in a study to assess the effects of the cholesterol inclusion complex on cellular cholesterol levels. It has also been used in a study to investigate the enantioseparation of catechin and epicatechin.

Code de la classe de stockage

13 - Non 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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Enantioseparation of catechin and epicatechin in plant food by chiral capillary electrophoresis

Kofink, M., et al.

European Food Research and Technology, 225, 569-577 (2007)

Oligomeric and functional properties of a debranching enzyme (TreX) from the archaeon Sulfolobus solfataricus P2

Park, J., et al.

Biocatalysis and Biotransformation, 26, 76-85 (2008)

N.m.r. study on the formation and geometry of inclusion complexes of 6-O-(alpha-maltosyl)cyclomalto-hexaose and -heptaose with p-nitrophenol in aqueous solution.

Y Inoue et al.

Carbohydrate research, 226(2), 197-208 (1992-03-30)

The formation and molecular geometry of inclusion complexes of some branched cyclomaltaoses with p-nitrophenol in aqueous solution have been investigated by using high-resolution 1H-n.m.r. spectroscopy. 6-O-(alpha-Maltosyl)cyclomalto-hexaose and -heptaose were found to form 1:1 inclusion complexes with p-nitrophenol, and the dissociation

Improvement of stability and dissolution of prostaglandin E1 by maltosyl-beta-cyclodextrin in lyophilized formulation.

M Yamamoto et al.

Chemical & pharmaceutical bulletin, 40(3), 747-751 (1992-03-01)

Protection afforded by maltosyl-beta-cyclodextrin against alpha-chymotrypsin-catalyzed hydrolysis of a luteinizing hormone-releasing hormone agonist, buserelin acetate.

K Matsubara et al.

Pharmaceutical research, 14(10), 1401-1405 (1997-11-14)

The present study addresses how maltosyl-beta-cyclodextrin (G2-beta-CyD) impacts upon the alpha-chymotrypsin-catalyzed hydrolysis of buserelin acetate, an agonist of luteinizing hormone-releasing hormone with emphasis upon the direct effect of G2-beta-CyD on the activity of the protease. Kinetic and solubility studies were

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