γ-(3-Pyridyl)-L-β-homoalanine dihydrochloride
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γ-(3-Pyridyl)-L-β-homoalanine dihydrochloride

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Category
β−Amino Acids
Catalog number
BAT-002562
CAS number
1217661-66-9
Molecular Formula
C9H14Cl2N2O2
Molecular Weight
253.13
IUPAC Name
(3S)-3-amino-4-pyridin-3-ylbutanoic acid;dihydrochloride
Synonyms
H-Ala(3-Pyri)-OH 2HCl; (S)-3-Amino-4-(3-pyridyl)butanoic acid dihydrochloride
Purity
> 95%
Storage
Store at RT
InChI
InChI=1S/C9H12N2O2.2ClH/c10-8(5-9(12)13)4-7-2-1-3-11-6-7;;/h1-3,6,8H,4-5,10H2,(H,12,13);2*1H/t8-;;/m0../s1
InChI Key
JOYZJLGIWVGPRK-JZGIKJSDSA-N
Canonical SMILES
C1=CC(=CN=C1)CC(CC(=O)O)N.Cl.Cl

γ-(3-Pyridyl)-L-β-homoalanine dihydrochloride is a specialized chemical compound renowned for its diverse applications in biochemical and pharmaceutical research. Here are the key applications highlighted with elevated perplexity and burstiness:

Neuroscience Research: Delving into neurotransmitter pathways, particularly the nicotinic acetylcholine receptors, γ-(3-Pyridyl)-L-β-homoalanine dihydrochloride plays a crucial role in unraveling the intricacies of neurological disorders and addiction. Researchers can decipher its interactions with these receptors, shedding light on underlying mechanisms and paving the way for innovative treatments targeting these pathways.

Drug Metabolism Studies: Serving as a vital substrate in exploring the activities of key enzymes involved in drug metabolism, such as cytochrome P450 enzymes, this compound offers valuable insights into enzyme specificity and kinetics. By observing the metabolism of γ-(3-Pyridyl)-L-β-homoalanine dihydrochloride, scientists can foresee potential drug interactions and tailor medical interventions to individual patients, enhancing personalized healthcare approaches.

Radiolabeling: Enabling the synthesis of radiolabeled analogs for advanced imaging studies, γ-(3-Pyridyl)-L-β-homoalanine dihydrochloride empowers researchers to visualize biological processes in vivo through positron emission tomography (PET) scans. This application proves invaluable for tracking disease progression and monitoring therapeutic responses, offering a non-invasive window into physiological dynamics.

Chemical Synthesis and Modification: Acting as a fundamental building block in the synthesis of diverse organic molecules, this compound's unique structure allows for versatile incorporation into backbone modifications for peptides and proteins. Its pivotal role in medicinal chemistry facilitates the development of novel therapeutic agents, showcasing its significance in fostering innovation and progress in pharmaceutical research.

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