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Catalog Number:
33636
CAS Number:
151074-96-3
α-méthyl-L-propargylglycine
Synonym(s):
α-Me-L-Pra-OH, ( Acide S -2-amino-2-méthyl-4-pentynoïque, Η-α-Me-Pra-OH
Documents
$100.05 /25 mg
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Product Information

a-Methyl-L-propargylglycine is a potent and selective inhibitor of the enzyme S-adenosylhomocysteine hydrolase, making it a valuable tool in biochemical research and drug development. This compound is recognized for its role in modulating methylation processes, which are critical in various biological systems. Its unique structure allows it to effectively interact with target enzymes, providing researchers with a means to explore metabolic pathways and potential therapeutic applications.

In the pharmaceutical industry, a-Methyl-L-propargylglycine has shown promise in studies related to neuroprotection and cancer therapy, where it may help in regulating cellular processes that are often dysregulated in disease states. Additionally, its ability to influence homocysteine levels makes it relevant in cardiovascular research. Researchers and industry professionals can leverage this compound to gain insights into metabolic disorders and develop innovative solutions for health challenges.

Synonyms
α-Me-L-Pra-OH, ( Acide S -2-amino-2-méthyl-4-pentynoïque, Η-α-Me-Pra-OH
CAS Number
151074-96-3
Molecular Formula
C 6 H 9 NO 2
Molecular Weight
127.14
MDL Number
MFCD12198154
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
α-Me-L-Pra-OH, ( Acide S -2-amino-2-méthyl-4-pentynoïque, Η-α-Me-Pra-OH
CAS Number
151074-96-3
Molecular Formula
C 6 H 9 NO 2
Molecular Weight
127.14
MDL Number
MFCD12198154
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

a-Methyl-L-propargylglycine is widely utilized in research focused on:

  • Neuroscience Research: This compound serves as a potent inhibitor of the enzyme S-adenosylhomocysteine hydrolase, which is crucial in studies related to neurotransmitter regulation and neuroprotection.
  • Cardiovascular Studies: Its ability to modulate homocysteine levels makes it valuable in researching cardiovascular diseases, helping to understand and potentially mitigate risks associated with high homocysteine levels.
  • Metabolic Disorders: Researchers explore its role in metabolic pathways, particularly in conditions like diabetes, where it may influence insulin sensitivity and glucose metabolism.
  • Pharmaceutical Development: The compound is investigated for its potential therapeutic applications, particularly in developing drugs targeting neurological and metabolic disorders, offering a unique mechanism of action compared to traditional treatments.
  • Biochemical Assays: It is frequently used in laboratory assays to study enzyme activity and metabolic processes, providing insights that can lead to innovative solutions in biochemistry and pharmacology.

Citations