3-(2'-Pyridyl)-D-alanine Dihydrochloride
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3-(2'-Pyridyl)-D-alanine Dihydrochloride

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Category
D-Amino Acids
Catalog number
BAT-007803
CAS number
74104-85-1
Molecular Formula
C8H10N2O2·2HCl
Molecular Weight
239.09
IUPAC Name
(2R)-2-amino-3-pyridin-2-ylpropanoic acid;dihydrochloride
Synonyms
D-Ala(2'-pyridyl)-OH 2HCl; (R)-2-Amino-3-(2-pyridyl)propionic acid dihydrochloride; (R)-2-Amino-3-(pyridin-2-yl)propanoic acid dihydrochloride; 3-Pyridin-2-yl-D-alanine-hydrogen chloride; (2R)-2-amino-3-pyridin-2-ylpropanoic acid dihydrochloride
Related CAS
37535-52-7 (free base)
Appearance
White to off-white powder
Purity
≥ 99% (HPLC)
Melting Point
182-187 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C8H10N2O2.2ClH/c9-7(8(11)12)5-6-3-1-2-4-10-6;;/h1-4,7H,5,9H2,(H,11,12);2*1H/t7-;;/m1../s1
InChI Key
HGOJCMDWQOEDJA-XCUBXKJBSA-N
Canonical SMILES
C1=CC=NC(=C1)CC(C(=O)O)N.Cl.Cl

3-(2'-Pyridyl)-D-alanine Dihydrochloride, a versatile chemical compound with diverse applications in scientific research. Here are the key applications presented with high perplexity and burstiness:

Neuroscience Research: A key player in neuroscience, this compound serves as a valuable tool for delving into neurotransmitter systems, acting as an analog of amino acids. Researchers leverage its properties to unravel the intricate mechanisms governing neurotransmitter synthesis, release, and uptake within neural tissues. This exploration offers profound insights into the complexities of brain function, shedding light on conditions like epilepsy and neurodegenerative diseases.

Pharmacological Studies: Embracing the realm of pharmacology, 3-(2'-Pyridyl)-D-alanine Dihydrochloride emerges as a pivotal component in investigating the impacts of structural modifications on bioactive molecules. It serves as a conduit for probing receptor-ligand interactions, opening doors to the realm of potential drug candidates. The compound's unique affinities with biological targets serve as a beacon, guiding the exploration of pharmacodynamics and pharmacokinetics of emerging therapeutic agents.

Biochemistry Research: Unveiling the mysteries of enzyme kinetics and mechanisms, this compound finds its niche in biochemistry as a substrate analog for probing enzymatic reactions involving amino acids and their derivatives. Scientists harness its capabilities to decipher the intricate pathways through which enzymes catalyze reactions. This knowledge is pivotal in designing enzyme inhibitors with therapeutic potential, paving the way for innovative drug development strategies.

Chromatography Studies: Taking center stage in chromatography, 3-(2'-Pyridyl)-D-alanine Dihydrochloride emerges as a key reagent for unraveling complex mixtures of biomolecules. Its distinctive chemical properties serve as a catalyst for developing cutting-edge chromatographic techniques geared towards separating amino acids and peptides. This breakthrough not only facilitates the exploration of metabolic profiles but also streamlines the purification of biologically active compounds in both research and industrial settings.

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