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Catalog Number:
03339
CAS Number:
72669-53-5
L-Glutamic acid γ-7-amido-4-methylcoumarin
Purity:
≥ 99% (HPLC)
Synonym(s):
L-Glu(AMC)-OH, L-Glutamic acid 5-(7-amido-4-methylcoumarin)
Documents
$141.41 /100MG
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Product Information

L-Glutamic acid g-7-amido-4-methylcoumarin is a versatile compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound, a derivative of L-Glutamic acid, features a unique coumarin moiety that enhances its fluorescent properties, making it an excellent choice for use in various assays and imaging techniques. Researchers often utilize this compound in enzyme activity studies, particularly in the investigation of proteases and other enzymes that interact with glutamic acid derivatives. Its ability to act as a substrate or inhibitor in biochemical pathways provides valuable insights into metabolic processes.

Moreover, L-Glutamic acid g-7-amido-4-methylcoumarin is instrumental in drug discovery, particularly in the development of therapeutic agents targeting neurological disorders. Its fluorescent characteristics allow for real-time monitoring of cellular processes, facilitating advancements in understanding disease mechanisms. The compound's stability and compatibility with various biological systems make it an essential tool for researchers aiming to explore the intricate roles of amino acids in cellular functions.

Synonyms
L-Glu(AMC)-OH, L-Glutamic acid 5-(7-amido-4-methylcoumarin)
CAS Number
72669-53-5
Purity
≥ 99% (HPLC)
Molecular Formula
C15H16N2O5
Molecular Weight
304.3
MDL Number
MFCD00038085
PubChem ID
4406900
Melting Point
190-196 °C (dec.)
Appearance
White crystalline powder
Optical Rotation
[α]D20 = +33 ± 2º (C=1, 50% in AcOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
L-Glu(AMC)-OH, L-Glutamic acid 5-(7-amido-4-methylcoumarin)
CAS Number
72669-53-5
Purity
≥ 99% (HPLC)
Molecular Formula
C15H16N2O5
Molecular Weight
304.3
MDL Number
MFCD00038085
PubChem ID
4406900
Melting Point
190-196 °C (dec.)
Appearance
White crystalline powder
Optical Rotation
[α]D20 = +33 ± 2º (C=1, 50% in AcOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

L-Glutamic acid g-7-amido-4-methylcoumarin is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as a fluorescent probe in biochemical assays, allowing researchers to visualize and track cellular processes in real-time.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in targeting specific receptors in neurological studies, enhancing therapeutic efficacy.
  • Biochemical Research: Used in studies related to neurotransmitter activity, it helps in understanding the mechanisms of synaptic transmission and potential treatments for neurological disorders.
  • Analytical Chemistry: This compound is applied in analytical methods to detect and quantify amino acids, providing accurate results in food and environmental testing.
  • Fluorescence Microscopy: It is utilized in fluorescence microscopy techniques, enabling detailed imaging of cellular structures and functions, which is essential for cellular biology research.

Citations