210110-89-7 Usage
Uses
Used in Histochemical Applications:
5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside is used as a histochemical substrate for the detection and analysis of a-N-acetyl-galactosaminidase enzyme activity. This application is crucial in research and diagnostic processes, as it helps identify and quantify the presence of this specific enzyme in various samples.
Used in Research and Diagnostics:
In the field of research and diagnostics, 5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside is used as a tool to study the function and role of a-N-acetyl-galactosaminidase. This enzyme is involved in the metabolism of certain glycoconjugates, and its activity can be indicative of various physiological or pathological conditions. By using 5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside as a substrate, researchers can gain insights into the enzyme's behavior and its potential role in disease processes.
Used in Pharmaceutical Development:
5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside may also be utilized in the development of pharmaceuticals targeting a-N-acetyl-galactosaminidase or related enzymes. By understanding the interactions between 5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside and the enzyme, researchers can design drugs that modulate enzyme activity, potentially leading to novel therapeutic strategies for conditions related to the dysregulation of this enzyme.
Used in Biochemical Education:
In the context of biochemical education, 5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside can be employed as a teaching aid to demonstrate enzyme-substrate interactions and the principles of enzyme kinetics. Students can use 5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside to perform experiments and gain a deeper understanding of the role of enzymes in biological processes.
Overall, 5-Bromo-4-chloro-3-indolyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside is a versatile compound with applications in various fields, including histochemistry, research and diagnostics, pharmaceutical development, and biochemical education. Its unique properties and role as a substrate for a-N-acetyl-galactosaminidase make it an important tool for advancing our understanding of enzyme function and its implications in health and disease.
Check Digit Verification of cas no
The CAS Registry Mumber 210110-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,1,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 210110-89:
(8*2)+(7*1)+(6*0)+(5*1)+(4*1)+(3*0)+(2*8)+(1*9)=57
57 % 10 = 7
So 210110-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H18BrClN2O6/c1-6(22)19-13-15(24)14(23)10(5-21)25-16(13)26-11-4-7-9(20-11)3-2-8(17)12(7)18/h2-4,10,13-16,20-21,23-24H,5H2,1H3,(H,19,22)/t10?,13-,14-,15+,16+/m0/s1
