β-(1-Cyclopentenyl)-DL-alanine
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β-(1-Cyclopentenyl)-DL-alanine

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Category
DL-Amino Acids
Catalog number
BAT-007508
CAS number
90087-65-3
Molecular Formula
C8H13NO2
Molecular Weight
155.19
β-(1-Cyclopentenyl)-DL-alanine
IUPAC Name
2-amino-3-(cyclopenten-1-yl)propanoic acid
Synonyms
H-DL-Ala(1-cPentenyl)-OH; H-β-(1-Cyclopentenyl)-DL-Ala-OH; 2-Amino-3-cyclopent-1-enyl-propionic acid; 2-Amino-3-cyclopent-1-enyl-propionsaeure; 2-amino-3-(cyclopent-1-en-1-yl)propanoic acid; 3-Cyclopent-1-en-1-ylalanine
Purity
95%
Density
1.168 g/cm3
Boiling Point
290.0 °C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C8H13NO2/c9-7(8(10)11)5-6-3-1-2-4-6/h3,7H,1-2,4-5,9H2,(H,10,11)
InChI Key
MNHWYCRCODAGAH-UHFFFAOYSA-N
Canonical SMILES
C1CC=C(C1)CC(C(=O)O)N

β-(1-Cyclopentenyl)-DL-alanine, also known as CPA, is an amino acid analog with diverse applications in scientific research and biotechnology. Here are the key applications of β-(1-Cyclopentenyl)-DL-alanine, presented with high perplexity and burstiness:

Enzyme Inhibition Studies: Utilizing β-(1-Cyclopentenyl)-DL-alanine as a tool for investigating enzyme inhibition, researchers delve into the realm of amino acid metabolism, unraveling the intricate dance of enzymes. By acting as a competitive inhibitor, this analog sheds light on enzyme-substrate interactions and kinetic properties, aiding in the crafting of tailored enzyme inhibitors for therapeutic ends.

Protein Synthesis Research: In the exploration of protein synthesis, β-(1-Cyclopentenyl)-DL-alanine emerges as a key player, seamlessly integrating into peptides to probe the influences of unconventional amino acids on protein structure and function. Researchers navigate the maze of protein folding, stability, and catalytic activity, manipulating side chains to sculpt novel proteins and peptides with desired characteristics, opening doors to uncharted protein landscapes.

Antibacterial Development: With its resemblance to natural amino acids, β-(1-Cyclopentenyl)-DL-alanine sparks curiosity in the realm of antibacterial properties. Researchers delve into uncharted territories, exploring the potential of this analog as a weapon against bacterial foes. By disrupting bacterial amino acid biosynthesis pathways, novel antimicrobial agents with unparalleled mechanisms of action against resistant strains may emerge, revolutionizing the battlefield against bacterial resistance.

Metabolic Pathway Elucidation: Serving as a beacon in the murky labyrinth of metabolic pathways, β-(1-Cyclopentenyl)-DL-alanine acts as a metabolic probe, illuminating the shadows of metabolic analysis. By incorporating this analog into metabolic studies, scientists embark on a journey of discovery, tracing and mapping specific pathways to reveal the secrets of enzymatic steps and regulatory nodes. This knowledge unlocks doors to the understanding of metabolic diseases and the engineering of metabolic pathways for biotechnological marvels.

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