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alpha-cyclodextrin

Known as: Alpha-Cycloamylose, cyclomaltohexaose, alpha-Dextrin 
National Institutes of Health

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Related topics

3 relations
0.5 ML Alprostadil 0.02 MG/ML Prefilled Syringe [Caverject]1 ML Alprostadil 0.02 MG/ML Cartridge [Edex]

Broader (1)

alpha-Cyclodextrins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Inclusion complexes of bisphenol A with cyclomaltoheptaose (beta-cyclodextrin): solubilization and structure.
2004
2004
Use of 13C chemical shift surfaces in the study of carbohydrate conformation. Application to cyclomaltooligosaccharides (cyclodextrins) in the solid state and in solution.
2004
2004
Cyclodextrin-Glucanotransferase von Klebsiella pneumoniae
Abstract1.The strain M 5 al of Klebsiella pneumoniae grows excellently with starches. We were able to show that besides the… 
2002
2002
Addition of maltodextrins to the nonreducing-end of acarbose by reaction of acarbose with cyclomaltohexaose and cyclomaltodextrin glucanyltransferase.
Highly Cited
1992
Highly Cited
1992
13C-CP/MAS NMR studies of the cyclomalto-oligosaccharide (cyclodextrin) hydrates.
1992
1992
Multiple tritylation: a convenient route to polysubstituted derivatives of cyclomaltohexaose.
Highly Cited
1982
Highly Cited
1982
Potentiometric study of molecular complexes of weak acids and bases applied to complexes of alpha-cyclodextrin with para-substituted benzoic acids.
The theory of the potentiometric methods of studying complexes of ionizable substrates was developed, nd graphical techniques are… 
1980
1980
The complexation chemistry of cycloamyloses: equilibrium constants by novel spectrophotometric methods.
Highly Cited
1976
Highly Cited
1976
Effect of cycloamyloses on apparent dissociation constants of carboxylic acids and phenols: equilibrium analytical selectivity induced by complex formation.
Apparent dissociation constants of organic acids were determined by potentiometric titration in the presence of cyclohexaamylose… 
Highly Cited
1974
Highly Cited
1974
Immobilization of ligands for biospecific affinity chromatography VIA their hydroxyl groups. the cyclohexaamylose‐β‐amylase system
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