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Catalog Number:
35143
CAS Number:
98891-36-2
Chlorhydrate de L-Homopropargylglycine
Purity:
≥ 95 % (RMN)
Documents
$117.50 /5 mg
Taille
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Informations sur le produit

L-Homopropargylglycine hydrochloride is a versatile compound recognized for its unique properties and applications in various fields, particularly in biochemical research and pharmaceutical development. This compound, a derivative of propargylglycine, is known for its role as an inhibitor of cystathionine gamma-lyase, making it a valuable tool in studies related to sulfur metabolism and hydrogen sulfide signaling pathways. Researchers utilize L-Homopropargylglycine hydrochloride to explore its potential therapeutic effects, particularly in neuroprotection and cardiovascular health, due to its ability to modulate endogenous hydrogen sulfide levels.

In addition to its research applications, L-Homopropargylglycine hydrochloride is also gaining attention in the synthesis of novel compounds, where its unique alkyne functional group can serve as a building block in organic synthesis. Its stability and solubility in various solvents enhance its usability in laboratory settings, making it an essential reagent for chemists and biochemists alike. With its growing relevance in both academic and industrial research, L-Homopropargylglycine hydrochloride stands out as a compound with significant potential for advancing scientific knowledge and developing innovative therapeutic strategies.

Numéro CAS 
98891-36-2
Formule moléculaire
C6H9NO2 · HCl
Poids moléculaire 
163.6
Informations générales
Numéro CAS 
98891-36-2
Formule moléculaire
C6H9NO2 · HCl
Poids moléculaire 
163.6
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

L-Homopropargylglycine hydrochloride is widely utilized in research focused on various applications:

  • Biochemical Research: This compound serves as a potent inhibitor of cystathionine γ-lyase, making it valuable for studying sulfur amino acid metabolism and its implications in diseases such as cancer.
  • Neuroscience: Researchers use it to explore its neuroprotective effects, particularly in models of neurodegenerative diseases, helping to understand mechanisms of neuronal survival.
  • Pharmaceutical Development: Its unique structure allows for the design of novel drugs targeting metabolic pathways, offering potential advantages over traditional compounds in specificity and efficacy.
  • Plant Biology: In agricultural studies, it aids in understanding plant responses to stress, contributing to the development of crops that can better withstand environmental challenges.
  • Analytical Chemistry: The compound is employed in various assays to measure enzyme activity, providing insights into metabolic disorders and potential therapeutic targets.

Citations