Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine
Need Assistance?
  • US & Canada:
    +
  • UK: +

Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
BOC-Amino Acids
Catalog number
BAT-002982
CAS number
200122-49-2
Molecular Formula
C21H34N4O7S
Molecular Weight
486.68
Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine
IUPAC Name
(2R)-5-[[amino-[(4-methoxy-2,3,6-trimethylphenyl)sulfonylamino]methylidene]amino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
Synonyms
Boc-D-Arg(Mtr)-OH; (R)-2-((Tert-Butoxycarbonyl)Amino)-5-(3-((4-Methoxy-2,3,6-Trimethylphenyl)Sulfonyl)Guanidino)Pentanoic Acid
Appearance
White to off-white powder
Purity
≥ 98% (HPLC)
Melting Point
92-97 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C21H34N4O7S/c1-12-11-16(31-7)13(2)14(3)17(12)33(29,30)25-19(22)23-10-8-9-15(18(26)27)24-20(28)32-21(4,5)6/h11,15H,8-10H2,1-7H3,(H,24,28)(H,26,27)(H3,22,23,25)/t15-/m1/s1
InChI Key
CXZHJRGYWGPJSD-OAHLLOKOSA-N
Canonical SMILES
CC1=CC(=C(C(=C1S(=O)(=O)NC(=NCCCC(C(=O)O)NC(=O)OC(C)(C)C)N)C)C)OC

Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine, a specialty chemical with diverse applications in bioscience and pharmaceutical research, plays a pivotal role in various scientific endeavors. Here are the key applications expounded with a high degree of perplexity and burstiness:

Peptide Synthesis: Acting as a shielded amino acid derivative, Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine is frequently harnessed in peptide synthesis. By employing the Boc (tert-butyloxycarbonyl) group, this compound safeguards against undesired side reactions during peptide chain assembly, facilitating the precise integration of arginine into synthetic peptides. These peptides are essential for both research endeavors and therapeutic applications, underscoring the significance of this process.

Protease Inhibitors: An essential constituent in the realm of protease inhibitors, this compound is instrumental in formulating potent inhibitors crucial for studying enzyme mechanisms and combating diseases like HIV and cancer. By incorporating this modified arginine into inhibitor constructs, scientists can craft highly specific and efficacious compounds, marking a milestone in drug development and disease management.

Receptor Binding Studies: Delving into receptor binding assays, Nα-Boc-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine is deployed to explore interactions with arginine-specific receptors. Unraveling these interactions unveils key insights into receptor bioactivity, paving the way for the creation of targeted therapies. This specialized knowledge proves invaluable in dissecting signaling pathways and deciphering cellular communication networks, reshaping the landscape of therapeutic research.

Structural Biology: In the intricate realm of structural biology, this compound finds its niche in crystallizing and analyzing protein structures. Through its incorporation into protein frameworks, researchers probe the effects of specific modifications on protein folding and stability. This critical information serves as the cornerstone for designing proteins endowed with enhanced stability and desired attributes for therapeutic applications, heralding a new era of protein engineering and drug development.

Online Inquiry
Verification code
Inquiry Basket