65615-60-3 Usage
Description
.beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is a chemical compound derived from D-galactose, a type of sugar. It is widely utilized in biochemical research as a substrate for the enzyme β-galactosidase. .beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate's tetrabenzoate group significantly improves its solubility and stability, facilitating its use in laboratory settings. .beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is essential for studying enzymes and their physiological functions, particularly in carbohydrate metabolism and degradation.
Uses
Used in Biochemical Research:
.beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is used as a substrate for the enzyme β-galactosidase in biochemical research. It aids in understanding the activity and function of this enzyme, which is crucial for carbohydrate metabolism and degradation.
Used in Enzyme Assays:
.beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is employed as a key component in enzyme assays, which are laboratory experiments designed to measure the activity of β-galactosidase. These assays are vital for studying the enzyme's role in various biological processes and its potential applications in medicine and biotechnology.
Used in Laboratory Experiments:
.beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is used in various laboratory experiments to investigate the activity of β-galactosidase and its interactions with other molecules. .beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate's enhanced solubility and stability make it an ideal choice for such experiments, allowing researchers to obtain accurate and reliable results.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, .beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is used as a research tool to develop new drugs and therapies targeting carbohydrate metabolism and related diseases. Its role in studying the enzyme β-galactosidase can lead to the discovery of novel treatments for conditions such as lysosomal storage disorders and other metabolic disorders.
Used in Diagnostic Applications:
.beta.-D-Galactopyranoside, phenyl 1-thio-, tetrabenzoate is also utilized in the development of diagnostic tools and tests for detecting and monitoring the activity of β-galactosidase. These diagnostic applications can help in the early detection and management of diseases associated with the malfunctioning of this enzyme, such as Gaucher's disease and Fabry disease.
Check Digit Verification of cas no
The CAS Registry Mumber 65615-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,1 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65615-60:
(7*6)+(6*5)+(5*6)+(4*1)+(3*5)+(2*6)+(1*0)=133
133 % 10 = 3
So 65615-60-3 is a valid CAS Registry Number.
65615-60-3Relevant articles and documents
Total Synthesis of a Partial Structure from Arabinogalactan and Its Application for Allergy Prevention
Krumb, Matthias,J?ger, Maximilian,Voss, Alice,Immig, Loreen,Peters, Karin,Kowalczyk, Danuta,Bufe, Albrecht,Opatz, Till,Holst, Otto,Vogel, Christian,Peters, Marcus
supporting information, p. 928 - 933 (2020/10/29)
Arabinogalactan, a microheterogeneous polysaccharide occurring in plants, is known for its allergy-protective activity, which could potentially be used for preventive allergy treatment. New treatment options are highly desirable, especially in a preventive manner, due to the constant rise of atopic diseases worldwide. The structural origin of the allergy-protective activity of arabinogalactan is, however, still unclear and isolation of the polysaccharide is not feasible for pharmaceutical applications due to a variation of the activity of the natural product and contaminations with endotoxins. Therefore, a pentasaccharide partial structure was selected for total synthesis and subsequently coupled to a carrier protein to form a neoglycoconjugate. The allergy-protective activity of arabinogalactan could be reproduced with the partial structure in subsequent in vivo experiments. This is the first example of a successful simplification of arabinogalactan with a single partial structure while retaining its allergy-preventive potential.
Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies
Fekete, Aniko,Borbas, Aniko,Antus, Sandor,Liptak, Andras
experimental part, p. 1434 - 1441 (2009/12/09)
Synthesis of tetra- and hexasaccharides built up from a β-(1→6)-linked galactopyranosyl backbone with arabinofuranosyl side chains at position 3 and with a 3-aminopropyl spacer related to arabinogalactans is described. These oligosaccharides were prepared
Scope and applications of "active and latent" thioglycosyl donors. Part 4
Cao, Suoding,Hernandez-Mateo, Fernando,Roy, Rene
, p. 609 - 631 (2007/10/03)
The relative reactivity of various thioglycosyl donors having ethyl, phenyl, or parasubstituted phenyl groups with electron donating (N-Ac) or electron withdrawing (NO2) substituents were compared using 1,2:3,4-di-O-isopropylidene-α-D-galactopy
