(R)-4-(Indol-3-yl)-β-homoalanine
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(R)-4-(Indol-3-yl)-β-homoalanine

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Category
β−Amino Acids
Catalog number
BAT-014145
CAS number
736131-01-4
Molecular Formula
C12H14N2O2
Molecular Weight
218.25
(R)-4-(Indol-3-yl)-β-homoalanine
IUPAC Name
(3R)-3-amino-4-(1H-indol-3-yl)butanoic acid
Synonyms
(R)-4-(Indol-3-yl)-β-homoalanine
Related CAS
477250-51-4 (hydrochloride)
Purity
95%
Density
1.311g/cm3
Boiling Point
462.3°C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H14N2O2/c13-9(6-12(15)16)5-8-7-14-11-4-2-1-3-10(8)11/h1-4,7,9,14H,5-6,13H2,(H,15,16)/t9-/m1/s1
InChI Key
DUVVFMLAHWNDJD-SECBINFHSA-N
Canonical SMILES
C1=CC=C2C(=C1)C(=CN2)CC(CC(=O)O)N

(R)-4-(Indol-3-yl)-β-homoalanine, a compound utilized in diverse research and industrial applications, holds significance in various fields. Here are the key applications, presented with a high degree of perplexity and burstiness:

Pharmaceutical Research: Playing a pivotal role in the quest for new therapeutic agents, (R)-4-(Indol-3-yl)-β-homoalanine offers an intriguing structure that allows researchers to delve into unexplored mechanisms of action and potential drug targets. By subjecting this compound to an array of biological assays, scientists can unearth novel pathways for the treatment and prevention of diseases, opening new avenues for medical innovation.

Synthetic Chemistry: In the realm of synthetic chemistry, (R)-4-(Indol-3-yl)-β-homoalanine serves as a versatile building block for the synthesis of intricate molecules. With its distinctive indole and β-homoalanine components, this compound acts as a flexible intermediate, enabling chemists to craft compounds with tailored properties for diverse applications, ranging from pharmaceuticals to materials science, fostering creativity in molecular design.

Neuroscience Research: Delving into the intricate workings of neurotransmitter systems and their impact on brain function, (R)-4-(Indol-3-yl)-β-homoalanine emerges as a valuable tool for neuroscience research. By incorporating this compound into experimental setups, researchers can explore its effects on neural signaling and plasticity, offering insights into neurological disorders and paving the way for novel treatments in the realm of mental health, illuminating the complexities of brain function.

Enzyme Inhibition Studies: In the realms of enzyme inhibition and binding affinity studies, (R)-4-(Indol-3-yl)-β-homoalanine serves as a vital tool. Researchers leverage this compound to interrogate inhibitory effects on diverse enzymes, unraveling the intricacies of enzyme-substrate interactions. Such findings play a crucial role in drug development, especially in the design of inhibitors targeting specific enzymatic pathways, propelling advancements in therapeutic interventions.

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