Nω-(2,2,4,6,7-Pentamethyldihydro-benzofuran-5-sulfonyl)-L-arginine allyl ester hydrochloride
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Nω-(2,2,4,6,7-Pentamethyldihydro-benzofuran-5-sulfonyl)-L-arginine allyl ester hydrochloride

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Category
L-Amino Acids
Catalog number
BAT-004154
CAS number
257288-23-6
Molecular Formula
C22H34N4O5S·HCl
Molecular Weight
503.12
Nω-(2,2,4,6,7-Pentamethyldihydro-benzofuran-5-sulfonyl)-L-arginine allyl ester hydrochloride
IUPAC Name
prop-2-enyl (2S)-2-amino-5-[[amino-[(2,2,4,6,7-pentamethyl-3H-1-benzofuran-5-yl)sulfonylamino]methylidene]amino]pentanoate;hydrochloride
Synonyms
L-Arg(Pbf)-OAll HCl; H-Arg(Pbf)-Allyl Ester HCl
Appearance
White to off-white solid
Purity
≥ 95% (HPLC)
Storage
Store at 2-8 °C
InChI
InChI=1S/C22H34N4O5S.ClH/c1-7-11-30-20(27)17(23)9-8-10-25-21(24)26-32(28,29)19-14(3)13(2)18-16(15(19)4)12-22(5,6)31-18;/h7,17H,1,8-12,23H2,2-6H3,(H3,24,25,26);1H/t17-;/m0./s1
InChI Key
AWGBWYKSQZNCFT-LMOVPXPDSA-N
Canonical SMILES
CC1=C2C(=C(C(=C1C)S(=O)(=O)NC(=NCCCC(C(=O)OCC=C)N)N)C)CC(O2)(C)C.Cl

Nω-(2,2,4,6,7-Pentamethyldihydro-benzofuran-5-sulfonyl)-L-arginine allyl ester hydrochloride, a compound of immense significance in biochemical and pharmaceutical research, showcases a plethora of applications. Here are the key applications of this compound, presented with a high level of perplexity and burstiness:

Enzyme Inhibition Studies: Positioned as a vital tool in the domain of enzyme inhibition, this compound plays a pivotal role in unraveling the complexities of enzyme inhibition, particularly focusing on nitric oxide synthases (NOS). Researchers leverage its multifaceted potential to delve into the intricate mechanisms of enzyme inhibition and craft inhibitors with profound therapeutic implications. The exploration of these intricate interactions bears the promise of unveiling innovative drugs for combating diverse ailments, notably cardiovascular diseases.

Drug Development: Engaged in pharmaceutical research, Nω-(2,2,4,6,7-Pentamethyldihydro-benzofuran-5-sulfonyl)-L-arginine allyl ester hydrochloride assumes a foundational role in the development of novel therapeutic agents. Its distinctive binding properties and activities position it as an optimal candidate for synthesizing derivatives with enhanced pharmacokinetic profiles.

Protein Interaction Analysis: Serving as a versatile tool, this compound enables the investigation of protein-protein interactions and conformational alterations within biomolecules. By masquerading as a specific ligand or inhibitor, researchers investigate the dynamics of protein interactions and their implications on biological functions.

Metabolic Pathway Research: Scientists employ this compound to dissect intricate metabolic pathways and elucidate the functions of specific enzymes within these interconnected systems. By impeding select steps in a pathway, researchers trace the movement of metabolic intermediates and their fluxes. This comprehensive understanding is pivotal for advancing metabolic engineering initiatives and fostering the development of biotechnological applications, including biofuel synthesis and innovations in synthetic biology.

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