Z-3-(1-naphthyl)-D-alanine
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Z-3-(1-naphthyl)-D-alanine

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Category
CBZ-Amino Acids
Catalog number
BAT-005742
CAS number
96402-43-6
Molecular Formula
C21H19NO4
Molecular Weight
349.37
Z-3-(1-naphthyl)-D-alanine
IUPAC Name
(2R)-3-naphthalen-1-yl-2-(phenylmethoxycarbonylamino)propanoic acid
Synonyms
Z-D-Ala(1-naphthyl)-OH; (2R)-2-([(Benzyloxy)carbonyl]amino)-3-naphthalen-1-yl-propionic acid
Appearance
White to off-white powder
Purity
≥ 99% (HPLC)
Melting Point
147-152 °C
Storage
Store at 2-8°C
InChI
InChI=1S/C21H19NO4/c23-20(24)19(22-21(25)26-14-15-7-2-1-3-8-15)13-17-11-6-10-16-9-4-5-12-18(16)17/h1-12,19H,13-14H2,(H,22,25)(H,23,24)/t19-/m1/s1
InChI Key
HNYQEAGTPQSPLT-LJQANCHMSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CC2=CC=CC3=CC=CC=C32)C(=O)O

Z-3-(1-naphthyl)-D-alanine, a specialized compound utilized in diverse biochemical and pharmacological investigations, boasts a multitude of applications. Here are the key applications highlighted with elevated perplexity and burstiness:

Receptor Binding Studies: Delving into receptor binding assays, researchers employ Z-3-(1-naphthyl)-D-alanine to explore the intricate interactions between ligands and their corresponding receptors. By harnessing this compound, scientists unveil binding affinities and kinetics shedding light on receptor functionality. This essential data underpins the development of drugs tailored to target specific receptors driving innovation in pharmacology.

Enzyme Inhibition Studies: Within the realm of enzyme inhibition mechanisms and kinetics, this compound serves as a potent tool. Functioning as a specialized inhibitor, Z-3-(1-naphthyl)-D-alanine aids in elucidating the pivotal role of target enzymes in metabolic pathways. Such studies fuel the discovery of new inhibitors poised to become potential therapeutic agents enriching the landscape of biochemical research and drug development.

Structure-Activity Relationship (SAR) Analysis: Playing a pivotal role in SAR investigations, Z-3-(1-naphthyl)-D-alanine unveils the intricate relationship between chemical structure and biological activity. Through meticulous analysis of this compound's effects on biological systems, researchers pinpoint critical molecular features that influence activity facilitating the rational design of more potent bioactive molecules. This sophisticated approach propels advancements in drug discovery and design.

Neuroscience Research: In the realm of neuroscience, Z-3-(1-naphthyl)-D-alanine becomes a cornerstone in unraveling the role of specific amino acids in neurotransmission and receptor functions. Its application aids in comprehending the modulation of synaptic activity and neural signaling pathways offering invaluable insights into the complexities of neural function. Knowledge gleaned from such studies propels the development of innovative therapies for neurological disorders pushing the boundaries of neuroscience research and therapeutic interventions.

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