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113079-84-8

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113079-84-8 Usage

Description

8-Hydroxyquinoline-β-D-galactopyranoside is a synthetic compound that serves as a chromogenic substrate for the enzyme β-D-galactosidase. It is characterized by its ability to produce a brown precipitate upon enzymatic cleavage, which makes it useful in various applications.

Uses

Used in Enzyme Assays:
8-Hydroxyquinoline-β-D-galactopyranoside is used as a chromogenic substrate for β-D-galactosidase assays. Its cleavage by the enzyme results in the formation of a brown precipitate, which allows for the detection and quantification of β-D-galactosidase activity in various samples.
Used in Research and Diagnostics:
In the field of research and diagnostics, 8-Hydroxyquinoline-β-D-galactopyranoside is employed as a tool for studying the activity and function of β-D-galactosidase. Its use in enzyme assays helps researchers and diagnosticians to evaluate the presence and activity of this enzyme in biological samples, which can be relevant for understanding certain metabolic processes and conditions.
Used in Pharmaceutical Development:
8-Hydroxyquinoline-β-D-galactopyranoside may also be utilized in the development of pharmaceuticals targeting β-D-galactosidase or related enzymes. Its role as a substrate can aid in the screening and optimization of potential drug candidates that modulate the activity of these enzymes, contributing to the advancement of therapeutic agents for various diseases and conditions.
Used in Educational Purposes:
In educational settings, 8-Hydroxyquinoline-β-D-galactopyranoside can be employed as a teaching aid to demonstrate enzyme-substrate interactions and the principles of enzyme kinetics. By using this chromogenic substrate in classroom experiments, students can gain hands-on experience in understanding the behavior of enzymes and their substrates, fostering a deeper comprehension of biochemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 113079-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113079-84:
(8*1)+(7*1)+(6*3)+(5*0)+(4*7)+(3*9)+(2*8)+(1*4)=108
108 % 10 = 8
So 113079-84-8 is a valid CAS Registry Number.

113079-84-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-quinolin-8-yloxyoxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names 8-Hydroxyquinoline-b-D-galactopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:113079-84-8 SDS

113079-84-8Relevant articles and documents

Synthesis of 8-hydroxyquinoline glycoconjugates and preliminary assay of their β1,4-GalT inhibitory and anti-cancer properties

Krawczyk, Monika,Pastuch-Gawolek, Gabriela,Mrozek-Wilczkiewicz, Anna,Kuczak, Michal,Skonieczna, Magdalena,Musiol, Robert

, p. 326 - 338 (2019)

8-Hydroxyquinoline scaffold is a privileged structure used in designing a new active agents with therapeutic potential. Its connections with the sugar unit is formed to improve the pharmacokinetic properties. The broad spectrum of activity of quinoline derivatives, especially glycoconjugates, is often associated with the ability to chelate metal ions or with the ability to intercalate into DNA. Simple and effective methods of synthesis glycoconjugates of 8-hydroxyquinoline and 8-hydroxyquinaldine derivatives, containing an O-glycosidic bond or a 1,2,3-triazole linker in their structure, have been developed. The obtained glycoconjugates were tested for their ability to inhibit β-1,4-Galactosyltransferase, as well as inhibit cancer cell proliferation. It was found that used glycoconjugation strategy influenced both improvement of activity and improvement of the bioavailability of 8-HQ derivatives. Their activity depends on type of attached sugar, presence of protecting groups in sugar moiety and presence of a linker between sugar and quinolone aglycone.

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