H-Ala(2-pyrideyl)-OH 2HCl
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H-Ala(2-pyrideyl)-OH 2HCl

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Category
L-Amino Acids
Catalog number
BAT-002102
CAS number
1082692-96-3
Molecular Formula
C8H10N2O2·2HCl
Molecular Weight
239.2
IUPAC Name
(2S)-2-amino-3-pyridin-2-ylpropanoic acid;dihydrochloride
Synonyms
H-L-2PAL-OH 2HCL; (S)-Pyridylalanine
Purity
98%
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-;;/m0../s1
InChI Key
HGOJCMDWQOEDJA-KLXURFKVSA-N
Canonical SMILES
C1=CC=NC(=C1)CC(C(=O)O)N.Cl.Cl

H-Ala(2-pyrideyl)-OH 2HCl, a modified amino acid with diverse applications in bioscience research, presents a plethora of opportunities. Here are the key applications, crafted with a high degree of perplexity and burstiness:

Peptide Synthesis: Serving as a fundamental component in peptide synthesis, H-Ala(2-pyrideyl)-OH 2HCl acts as a pivotal building block for peptides with tailored functional attributes. Its distinctive structure allows for the incorporation of pyridyl groups within peptides, augmenting binding affinity and specificity in biochemical assays. This feature is particularly advantageous in the creation of peptides for drug discovery and therapeutic interventions, heralding a new era of targeted treatments.

Protein Structure Studies: Leading the charge in protein structure exploration, the integration of H-Ala(2-pyrideyl)-OH 2HCl into protein sequences serves as a dynamic tool for investigating protein-ligand interactions. The pyridyl group functions as a catalyst for covalent modifications or coordination bonds, facilitating the probing of protein folding and conformational dynamics. This breakthrough aids in the elucidation of protein functional sites and sheds light on their mechanisms of action, unlocking the secrets of intricate biological machinery.

Bioconjugation: Embracing the realm of bioconjugation, H-Ala(2-pyrideyl)-OH 2HCl plays a pivotal role in linking bioactive molecules to peptides and proteins. The pyridyl group exhibits a remarkable ability to form stable bonds with diverse functional groups, enabling the creation of conjugates with tailored properties. These bioconjugates lie at the heart of targeted drug delivery, imaging techniques, and diagnostic applications, revolutionizing the landscape of precision medicine and investigative technologies.

Chemical Biology: Positioned at the forefront of chemical biology, researchers leverage the versatility of H-Ala(2-pyrideyl)-OH 2HCl to manipulate and dissect biological systems at the molecular level. Its adaptable reactivity makes it a cornerstone in chemical biology experiments, allowing for the modification of amino acids to unravel their roles in biochemical pathways. This critical insight into cellular processes not only reveals the intricacies of molecular interactions but also unveils novel therapeutic targets, paving the way for groundbreaking advancements in biomedicine.

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