H-D-Ala(4-pyridyl)-OH 2HCl
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H-D-Ala(4-pyridyl)-OH 2HCl

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Category
D-Amino Acids
Catalog number
BAT-000864
CAS number
174096-41-4
Molecular Formula
C8H10N2O2·2HCl
Molecular Weight
239.1
H-D-Ala(4-pyridyl)-OH 2HCl
IUPAC Name
(2R)-2-amino-3-pyridin-4-ylpropanoic acid;dihydrochloride
Synonyms
3-(4-Pyridyl)-D-alanine dihydrochloride; (2R)-2-amino-3-pyridin-4-ylpropanoic acid dihydrochloride
Purity
95%
Storage
Store at 2-8 °C
InChI
InChI=1S/C8H10N2O2.2ClH/c9-7(8(11)12)5-6-1-3-10-4-2-6;;/h1-4,7H,5,9H2,(H,11,12);2*1H/t7-;;/m1../s1
InChI Key
NAMMTAFKUFJMSD-XCUBXKJBSA-N
Canonical SMILES
C1=CN=CC=C1CC(C(=O)O)N.Cl.Cl

H-D-Ala(4-pyridyl)-OH 2HCl, a versatile amino acid derivative with manifold applications in bioscience and pharmaceutical research, finds its utility in various realms. Here are the key applications elucidated with high perplexity and burstiness:

Peptide Synthesis: Esteemed for its role in peptide synthesis, H-D-Ala(4-pyridyl)-OH 2HCl stands as a cornerstone in the creation of peptides for diverse research and therapeutic ventures. The exceptional pyridyl group embedded within this compound enables the incorporation of innovative functional groups, streamlining peptide bonding processes. Harnessing this compound in peptide chains fosters the development of exquisitely specific and functional peptides tailored for experimental explorations.

Drug Development: At the forefront of drug innovation, this compound serves as a catalyst for designing and synthesizing novel drug candidates. By integrating H-D-Ala(4-pyridyl)-OH 2HCl into small molecules or peptide-based drugs, researchers embark on a journey to unravel its pharmacological prowess. The inclusion of this compound may elevate the bioavailability, stability, and efficacy of resultant drug candidates, heralding new advancements in pharmaceutical landscapes.

Protein-Protein Interaction Studies: Delving into the intricacies of protein interactions and enzyme mechanisms, H-D-Ala(4-pyridyl)-OH 2HCl emerges as a pivotal tool. Through its integration into proteins or peptides, researchers unlock pathways to explore binding interactions, conformational shifts, and functional consequences. This exploration is paramount in deciphering molecular intricacies, paving the way for the development of inhibitors or modulators targeting specific protein interactions.

Bioconjugation: Embracing the realm of bioconjugation, this compound showcases its versatility by serving as a linchpin in linking proteins, peptides, or other biomolecules with a myriad of functional groups. The pyridyl group nestled within offers an adaptable anchor for covalently attaching to diverse molecules, enabling the creation of conjugates with myriad biomedical applications. These bioconjugates find utility in imaging techniques, targeted drug delivery systems, and diagnostic applications, pushing the boundaries of biomedicine.

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