Nα-Boc-Nω-nitro-L-arginine
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Nα-Boc-Nω-nitro-L-arginine

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Category
BOC-Amino Acids
Catalog number
BAT-002989
CAS number
2188-18-3
Molecular Formula
C11H21N5O6
Molecular Weight
319.30
Nα-Boc-Nω-nitro-L-arginine
IUPAC Name
(2S)-5-[[amino(nitramido)methylidene]amino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
Synonyms
Boc-L-Arg(NO2)-OH; N2-[(1,1-Dimethylethoxy)Carbonyl]-N5-[Imino(Nitroamino)Methyl]-L-Ornithine; N2-((1,1-Dimethylethoxy)Carbonyl)-N5-(Imino(Nitroamino)Methyl)-L-Ornithine
Purity
≥ 99% (HPLC)
Density
1.40±0.1 g/cm3(Predicted)
Melting Point
113-117 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C11H21N5O6/c1-11(2,3)22-10(19)14-7(8(17)18)5-4-6-13-9(12)15-16(20)21/h7H,4-6H2,1-3H3,(H,14,19)(H,17,18)(H3,12,13,15)/t7-/m0/s1
InChI Key
OZSSOVRIEPAIMP-ZETCQYMHSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CCCN=C(N)N[N+](=O)[O-])C(=O)O

Nα-Boc-Nω-nitro-L-arginine, a widely utilized inhibitor in biochemical and pharmacological research, exhibits a specific affinity for nitric oxide synthase (NOS). Here are the key applications of Nα-Boc-Nω-nitro-L-arginine presented with high perplexity and burstiness:

Enzyme Inhibition Studies: Acting as a potent inhibitor of NOS enzymes, Nα-Boc-Nω-nitro-L-arginine assists researchers in unraveling the intricate roles of nitric oxide (NO) in both physiological and pathological contexts. By impeding NO production, scientists can delve into the repercussions of reduced NO levels on cellular processes and disease pathologies. Particularly, this inhibitor plays a pivotal role in cardiovascular and neurological investigations, shedding light on the interplay between NO and disease mechanisms through precise enzymatic control.

Drug Development: Embraced in pharmaceutical exploration, Nα-Boc-Nω-nitro-L-arginine emerges as a key player in screening potential drug candidates targeting NOS. Its inhibitory prowess serves as a robust model for assessing the effectiveness of novel therapeutic agents aimed at modulating NO pathways. This aids in the creation of pharmacological interventions for manifold conditions, ranging from hypertension to inflammation and neurodegenerative disorders, offering a nuanced understanding of how NOS modulation can influence disease progression at the molecular level.

Signal Transduction Research: Nα-Boc-Nω-nitro-L-arginine acts as a powerful tool for dissecting NO signaling cascades across diverse cell populations. By thwarting NOS activity, researchers can delve into the intricate web of downstream signaling events influenced by alterations in NO levels. This comprehensive approach fuels a deeper comprehension of how NO orchestrates physiological and pathological responses at the cellular level, unravelling the complex interplay between NO signaling and intracellular communication with a finesse that opens new avenues for therapeutic interventions.

Physiological Function Studies: In the realm of experimental physiology, Nα-Boc-Nω-nitro-L-arginine serves as a cornerstone for exploring the multifaceted role of NO in upholding homeostasis and organ functionality. Researchers leverage this compound to dissect NO's impact on diverse physiological processes, including vascular tone regulation, neurotransmission modulation, and immune response orchestration. These in-depth insights form the bedrock for devising innovative strategies to combat diseases stemming from dysregulated NO production, offering a roadmap towards tailored therapeutics addressing diverse pathological conditions.

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