γ-(3-Benzothienyl)-L-β-homoalanine hydrochloride
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γ-(3-Benzothienyl)-L-β-homoalanine hydrochloride

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Category
β−Amino Acids
Catalog number
BAT-002560
CAS number
331847-09-7
Molecular Formula
C12H14ClNO2S
Molecular Weight
271.76
IUPAC Name
(3S)-3-amino-4-(1-benzothiophen-3-yl)butanoic acid;hydrochloride
Synonyms
L-β-HomoAla(3-benzothienyl)-OH HCl; (3-Benzothienyl)-L-β-homoalanine hydrochloride
Appearance
White Powder
Purity
≥ 99% by TLC
Melting Point
222-228 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H13NO2S.ClH/c13-9(6-12(14)15)5-8-7-16-11-4-2-1-3-10(8)11;/h1-4,7,9H,5-6,13H2,(H,14,15);1H/t9-;/m0./s1
InChI Key
WBZKGWWYBOKXAS-FVGYRXGTSA-N
Canonical SMILES
C1=CC=C2C(=C1)C(=CS2)CC(CC(=O)O)N.Cl

γ-(3-Benzothienyl)-L-β-homoalanine hydrochloride, a distinctive compound with diverse applications in bioscience research, is explored in various realms. Here are the key applications presented with high perplexity and burstiness:

Drug Development: In the realm of drug discovery, γ-(3-Benzothienyl)-L-β-homoalanine hydrochloride emerges as a promising candidate for therapeutic interventions. Its intricate molecular structure positions it as a contender for targeting specific disease pathways, particularly in conditions like cancer or neurodegenerative disorders. Researchers delve into its pharmacokinetics and efficacy, striving to unveil novel medications that could revolutionize treatment strategies.

Biochemical Research: Delving into biochemical investigations, this compound plays a pivotal role in elucidating enzyme interactions and binding kinetics. Through its integration into experimental setups, scientists unravel its impact on enzyme activity and substrate specificity. This intricate exploration sheds light on the underlying molecular mechanisms dictating enzyme functions, deepening our comprehension of biochemical processes at a fundamental level.

Protein Engineering: Serving as a valuable asset in the realm of protein engineering, γ-(3-Benzothienyl)-L-β-homoalanine hydrochloride facilitates in-depth studies of protein-protein interactions. Researchers leverage this compound to manipulate proteins, enabling a detailed examination of how specific amino acid modifications influence protein structure and function. This wealth of information fuels the design of proteins with augmented functionalities or novel characteristics, pushing the boundaries of protein engineering capabilities.

Neuroscience Research: In the domain of neuroscience, γ-(3-Benzothienyl)-L-β-homoalanine hydrochloride takes center stage in unraveling the intricacies of neural pathways and neurotransmitter systems. Its application in modulating neuronal activity opens doors to probing potential neuroprotective or neurotoxic effects. By dissecting its impact on the nervous system, researchers pave the way for innovative treatments targeting neurological disorders, propelling advancements in the field of neuroscience research.

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