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

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Category
β−Amino Acids
Catalog number
BAT-002564
CAS number
332061-92-4
Molecular Formula
C8H12ClNO2S
Molecular Weight
221.7
IUPAC Name
(3S)-3-amino-4-thiophen-3-ylbutanoic acid;hydrochloride
Synonyms
(3-Thienyl)-L-ß-homoalanine HCl; L-β-HomoAla(3-thienyl)-OH HCl
Appearance
White to off-white powder
Purity
≥ 98% by HPLC
Melting Point
187-192 °C
Boiling Point
340.9°C at 760mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C8H11NO2S.ClH/c9-7(4-8(10)11)3-6-1-2-12-5-6;/h1-2,5,7H,3-4,9H2,(H,10,11);1H/t7-;/m0./s1
InChI Key
QDZZLMYYGBIDFT-FJXQXJEOSA-N
Canonical SMILES
C1=CSC=C1CC(CC(=O)O)N.Cl

γ-(3-Thienyl)-L-β-homoalanine hydrochloride, a specialized compound with unique properties, finds value in diverse scientific research and biotechnological realms. Here are the key applications of this compound, presented with high perplexity and burstiness:

Chemical Synthesis: Serving as a pivotal building block in organic synthesis, γ-(3-Thienyl)-L-β-homoalanine hydrochloride enables the exploration of novel pathways for creating complex molecules. This compound's distinct structure propels chemists towards uncovering new avenues in organic chemistry, fostering the development of innovative compounds with potential therapeutic uses, particularly in drug discovery and the engineering of functional materials.

Proteomics Research: Crucial in the realm of proteomics, γ-(3-Thienyl)-L-β-homoalanine hydrochloride plays a fundamental role in deciphering protein structure and function. By incorporating this compound into peptides, researchers can achieve precise site-specific labeling and modifications, facilitating in-depth mass spectrometry analysis and the revelation of intricate protein interactions. This deeper understanding of proteomic landscapes is vital in advancing our knowledge of biological systems.

Neuroscience: Pioneering studies in neuroscience harness the potential of γ-(3-Thienyl)-L-β-homoalanine hydrochloride to delve into neurotransmitter systems and neural pathways. Integrating this compound into neural substrates allows scientists to probe its effects on synaptic activity and neural communication, paving the way for breakthroughs in treatments for debilitating neurological conditions like Alzheimer's and Parkinson's diseases. These investigations are pivotal in shaping the future of neuroscience research.

Biocatalysis: In the dynamic field of biocatalysis, γ-(3-Thienyl)-L-β-homoalanine hydrochloride emerges as a key tool for enhancing enzyme specificity and activity. Researchers leverage this compound to modify enzyme active sites, enhancing catalytic efficiency and substrate selectivity. This application holds significant promise in developing cutting-edge industrial biocatalysts for the streamlined production of fine chemicals and pharmaceuticals.

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