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Catalog Number:
29427
CAS Number:
947175-17-9
6-Cloro-4-metilumbeliferil β-D-glucurónido
Purity:
≥ 97 % (HPLC)
Documents
$153.63 /25 mg
Tamaño
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Product Information

6-Chloro-4-methylumbelliferyl β-D-glucuronide is a valuable compound widely utilized in biochemical research, particularly in the study of glucuronidation processes. This substrate is particularly significant for researchers investigating enzyme activity related to UDP-glucuronosyltransferases (UGTs), which play a crucial role in drug metabolism and detoxification pathways. Its unique structure allows for the sensitive detection of β-glucuronidase activity, making it an essential tool in various assays, including those aimed at understanding metabolic disorders and pharmacokinetics.

This compound's ability to fluoresce upon enzymatic hydrolysis provides a straightforward and effective method for quantifying enzyme activity, facilitating research in drug development and toxicology. Additionally, its application extends to the study of cellular processes and the development of therapeutic strategies targeting glucuronidation pathways. With its specific characteristics, 6-Chloro-4-methylumbelliferyl β-D-glucuronide stands out as a reliable choice for researchers seeking to enhance their understanding of metabolic processes and enzyme functions.

CAS Number
947175-17-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C16H15ClO9
Molecular Weight
386.74
MDL Number
MFCD15146339
PubChem ID
138109894
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
947175-17-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C16H15ClO9
Molecular Weight
386.74
MDL Number
MFCD15146339
PubChem ID
138109894
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Chloro-4-methylumbelliferyl b-D-glucuronide is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for glucuronidase enzymes, allowing researchers to measure enzyme activity in various biological samples, which is crucial for drug metabolism studies.
  • Biochemical Research: It is used in studies investigating glucuronidation, a key metabolic pathway for detoxifying drugs and environmental chemicals, providing insights into pharmacokinetics.
  • Fluorescent Probes: The compound exhibits fluorescence upon enzymatic cleavage, making it a valuable tool for visualizing enzyme activity in live cells or tissues, enhancing research in cellular biology.
  • Pharmaceutical Development: It aids in the evaluation of drug candidates by assessing their potential for glucuronidation, helping pharmaceutical companies optimize drug formulations for better efficacy and safety.
  • Toxicology Studies: The compound is employed in toxicological assessments to evaluate the metabolic pathways of potentially harmful substances, assisting in risk assessment and regulatory compliance.

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