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Sku CI21763_5_G
Chem Impex
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Product Information

Product Name
o-Nitrophenyl-1-thio-b-D-galactopyranoside
Brand Name
Chem Impex
Product Number
21763
CAS
1158-17-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
101992
IUPAC Name
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-(2-nitrophenyl)sulfanyloxane-3,4,5-triol
InChI Key
SZAOZNVCHHBUDZ-RUXWNWLUSA-N
SMILES
C1=CC=C(C(=C1)N+(=O)O-)SC@H2C@@H(C@H(C@H(C@H(O2)CO)O)O)O

Description

o-Nitrophenyl-1-thio-b-D-galactopyranoside is widely utilized in research focused on:

Enzyme Activity Assays: This compound serves as a substrate for various glycosidases, allowing researchers to measure enzyme activity in biochemical assays. Its ability to produce a color change upon hydrolysis makes it an effective tool for quantifying enzyme kinetics.

Biochemical Research: It is commonly used in studies involving carbohydrate metabolism and enzyme mechanisms, providing insights into how enzymes interact with substrates in biological systems.

Diagnostic Applications: The compound can be employed in diagnostic tests to identify specific enzyme deficiencies or activities in clinical samples, aiding in the diagnosis of metabolic disorders.

Drug Development: In pharmaceutical research, it helps in screening potential drug candidates that target glycosidases, which are important in various diseases, including cancer and infections.

Educational Purposes: It is often used in laboratory settings for teaching purposes, helping students understand enzyme-substrate interactions and the principles of enzymology through hands-on experiments.

References Data Source From Pubchem

Influence of Eight Unclassified Missense Variants of the MLH1 Gene on Lynch Syndrome Susceptibility

Publication Name: Biochemical Genetics
Publication Date: 2011-09-28
DOI: 10.1007/s10528-011-9467-z

Relaxed natural selection alone does not permit transposable element expansion within 4,000 generations in Escherichia coli

Publication Name: Genetica
Publication Date: 2011-07-13
DOI: 10.1007/s10709-011-9593-x

CCDC 156161: Experimental Crystal Structure Determination

Publication Date: 2001
DOI: 10.5517/cc57hgb

Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates: 2-nitrophenyl-β-<small>D</small>-thiogalactopyranoside

Publication Name: Acta crystallographica. Section C, Crystal structure communications
Publication Date: 2000-12-15
DOI: 10.1107/s0108270100012427