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Sku CI02852_25_G
Chem Impex
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Product Information

Product Name
3-(2-Naphthyl)-L-alanine
Brand Name
Chem Impex
Product Number
02852
CAS
58438-03-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
185915
IUPAC Name
(2S)-2-amino-3-naphthalen-2-ylpropanoic acid
InChI Key
JPZXHKDZASGCLU-LBPRGKRZSA-N
SMILES
C1=CC=C2C=C(C=CC2=C1)CC@@H(C(=O)O)N

Description

3-(2-Naphthyl)-L-alanine is widely utilized in research focused on:

Pharmaceutical Development: This compound is explored for its potential role in drug design, particularly in creating new therapies for neurological disorders due to its structural similarity to neurotransmitters.

Biochemical Research: It serves as a valuable tool in studying protein interactions and enzyme activity, helping researchers understand complex biological processes.

Material Science: The compound is investigated for its applications in developing novel materials, particularly in organic electronics, where its unique properties can enhance performance.

Food Industry: It is being studied for its potential use as a flavoring agent or additive, leveraging its aromatic characteristics to improve food products.

Cosmetic Formulations: The compound is also evaluated for its potential benefits in skincare products, where its properties may contribute to anti-aging effects and skin health.

References Data Source From Pubchem

TTD: Therapeutic Target Database describing target druggability information

Publication Name: Nucleic Acids Research
Publication Date: 2023-09-15
DOI: 10.1093/nar/gkad751

Electrochromic-Induced Rechargeable Aqueous Batteries: An Integrated Multifunctional System for Cross-Domain Applications

Publication Name: Nano-Micro Letters
Publication Date: 2023-04-07
DOI: 10.1007/s40820-023-01056-y

Case Study #6: [177Lu]Lu-DOTA-JR11: A Somatostatin Receptor Subtype 2 Antagonist for Radiopharmaceutical Therapy

Publication Name: Radiopharmaceutical Therapy
Publication Date: 2023
DOI: 10.1007/978-3-031-39005-0_16

Genetically programmed cell-based synthesis of non-natural peptide and depsipeptide macrocycles

Publication Name: Nature Chemistry
Publication Date: 2022-12-22
DOI: 10.1038/s41557-022-01082-0

Aldehyde-catalysed carboxylate exchange in α-amino acids with isotopically labelled CO2

Publication Name: Nature Chemistry
Publication Date: 2022-11-07
DOI: 10.1038/s41557-022-01074-0