H-Ala(3-pyridyl)-OMe 2HCl
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H-Ala(3-pyridyl)-OMe 2HCl

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Category
L-Amino Acids
Catalog number
BAT-002115
CAS number
327051-07-0
Molecular Formula
C9H12N2O2·2HCl
Molecular Weight
253.2
IUPAC Name
methyl (2S)-2-amino-3-pyridin-3-ylpropanoate;dihydrochloride
Synonyms
3-(3-pyridyl)alanine methyl ester dihydrochloride
Purity
95%
InChI
InChI=1S/C9H12N2O2.2ClH/c1-13-9(12)8(10)5-7-3-2-4-11-6-7;;/h2-4,6,8H,5,10H2,1H3;2*1H/t8-;;/m0../s1
InChI Key
XNSHHLGNMODFNC-JZGIKJSDSA-N
Canonical SMILES
COC(=O)C(CC1=CN=CC=C1)N.Cl.Cl

H-Ala(3-pyridyl)-OMe 2HCl, a compound with diverse applications in biochemical and pharmaceutical research, plays a pivotal role in various settings. Here are the key applications, presented with high perplexity and burstiness:

Peptide Synthesis: Acting as a fundamental component in peptide synthesis, H-Ala(3-pyridyl)-OMe 2HCl serves as a crucial building block for crafting peptides with specific functionalities. Its distinctive structure allows for the incorporation of pyridyl groups into peptides, potentially enhancing their binding affinity or biological activity. This process facilitates the generation of innovative peptides tailored for both research and therapeutic endeavors, advancing the frontiers of molecular biology.

Receptor Ligand Studies: Within the realm of studies investigating receptor-ligand interactions, H-Ala(3-pyridyl)-OMe 2HCl finds extensive utility, particularly in exploring receptors that demonstrate an affinity for amino acid derivatives. By integrating this compound into ligand molecules, researchers can delve into the binding sites and mechanisms of diverse receptors, shedding light on crucial aspects of drug design and cellular signaling pathways. This application stands as a cornerstone for deciphering intricate biological processes and designing targeted pharmaceutical interventions.

Enzyme Inhibition Assays: Offering a valuable tool for elucidating enzyme-inhibitor interactions, H-Ala(3-pyridyl)-OMe 2HCl is employed in enzyme inhibition assays to unravel the intricacies of enzyme kinetics and mechanisms of action. Whether serving as a substrate or inhibitor, this compound plays a pivotal role in drug discovery by providing insights into the interplay between enzymes and inhibitors. Such knowledge is instrumental in crafting enzyme-targeted therapies that hold promise for treating a myriad of medical conditions.

Pharmaceutical Research: In the realm of pharmaceutical research, H-Ala(3-pyridyl)-OMe 2HCl emerges as a key player in the development of novel drug candidates. Its unique structure can be optimized to enhance the pharmacokinetic and pharmacodynamic properties of potential medications, paving the way for the creation of safer and more effective pharmaceuticals. This application stands as a beacon of hope for the discovery of groundbreaking treatments across various medical domains, underscoring the compound's significance in driving therapeutic innovation.

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