Ac-D-Arg-OH
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Ac-D-Arg-OH

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Category
D-Amino Acids
Catalog number
BAT-015295
CAS number
2389-86-8
Molecular Formula
C8H16N4O3
Molecular Weight
216.24
Ac-D-Arg-OH
IUPAC Name
(2R)-2-acetamido-5-(diaminomethylideneamino)pentanoic acid
Synonyms
Nα-acetyl-D-arginine; N-acetyl-D-arginine; N2-Acetyl-D-arginine; Acetyl-D-arginine
Appearance
White Powder
Purity
95%
Density
1.39±0.1 g/cm3 (Predicted)
Melting Point
270°C
Storage
Store at RT
Solubility
Soluble in DMSO
InChI
InChI=1S/C8H16N4O3/c1-5(13)12-6(7(14)15)3-2-4-11-8(9)10/h6H,2-4H2,1H3,(H,12,13)(H,14,15)(H4,9,10,11)/t6-/m1/s1
InChI Key
SNEIUMQYRCDYCH-ZCFIWIBFSA-N
Canonical SMILES
CC(=O)NC(CCCN=C(N)N)C(=O)O

Ac-D-Arg-OH, a synthetic derivative of the amino acid arginine, plays a pivotal role in biomedical research and pharmaceutical development. Here are the key applications of Ac-D-Arg-OH presented with high perplexity and burstiness:

Peptide Synthesis: Serving as a foundational component in peptide and protein synthesis, Ac-D-Arg-OH is integral to constructing peptide chains that unravel protein structures and functions. This functionality is paramount in crafting therapeutic peptides and delving into intricate enzyme-substrate dynamics, paving the way for innovative therapeutic breakthroughs and profound insights into molecular interactions.

Cell Penetrating Peptides (CPPs): Within the realm of cell biology, Ac-D-Arg-OH takes center stage in sculpting cell-penetrating peptides that act as gateways for delivering therapeutic compounds into cells. CPPs incorporating Ac-D-Arg-OH act as molecular couriers, ferrying nucleic acids, proteins, and small molecules across cellular barriers. This transformative application is essential for designing advanced intracellular delivery systems vital for gene therapies and drug dissemination strategies.

Enzyme Inhibition Studies: Enabling researchers to delve into the intricate realms of enzyme dynamics, Ac-D-Arg-OH functions as a versatile tool in enzyme activity assays by mimicking substrates and serving as an inhibitor. Through unraveling the mechanisms of enzyme inhibition, researchers gain crucial insights that inform the design of cutting-edge enzyme inhibitors with potential therapeutic applications, ushering in a new era of pharmaceutical innovation.

Antimicrobial Research: In the pursuit of combating microbial threats, Ac-D-Arg-OH emerges as a promising candidate for exploring its antimicrobial properties, particularly in combating bacterial and viral pathogens. Its efficacy in disrupting microbial structures and impeding microbial enzymes opens up new avenues for developing potent antimicrobial agents and deciphering resistance mechanisms, bolstering efforts in combating infectious diseases and safeguarding public health.

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