N-α-[2-(4-Biphenyl)isopropyloxycarbonyl]-N-ω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine
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N-α-[2-(4-Biphenyl)isopropyloxycarbonyl]-N-ω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine

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Category
L-Amino Acids
Catalog number
BAT-005917
CAS number
117368-03-3
Molecular Formula
C32H40N4O7S
Molecular Weight
624.75
N-α-[2-(4-Biphenyl)isopropyloxycarbonyl]-N-ω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine
IUPAC Name
(2S)-5-[[amino-[(4-methoxy-2,3,6-trimethylphenyl)sulfonylamino]methylidene]amino]-2-[2-(4-phenylphenyl)propan-2-yloxycarbonylamino]pentanoic acid
Synonyms
Bpoc-Arg(Mtr)-OH
Storage
Store at -20°C
InChI
InChI=1S/C32H40N4O7S/c1-20-19-27(42-6)21(2)22(3)28(20)44(40,41)36-30(33)34-18-10-13-26(29(37)38)35-31(39)43-32(4,5)25-16-14-24(15-17-25)23-11-8-7-9-12-23/h7-9,11-12,14-17,19,26H,10,13,18H2,1-6H3,(H,35,39)(H,37,38)(H3,33,34,36)/t26-/m0/s1
InChI Key
GEZQNQFCUUSBHJ-SANMLTNESA-N
Canonical SMILES
CC1=CC(=C(C(=C1S(=O)(=O)NC(=NCCCC(C(=O)O)NC(=O)OC(C)(C)C2=CC=C(C=C2)C3=CC=CC=C3)N)C)C)OC

N-α-[2-(4-Biphenyl)isopropyloxycarbonyl]-N-ω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine, a complex chemical compound with diverse scientific research and biotechnological applications. Here are the key applications:

Peptide Synthesis: Acting as a protective shield in peptide synthesis, this compound ensures the preservation of specific amino acid residues, preventing unwanted reactions at crucial stages. It introduces selectivity and stability into the synthetic process, enabling researchers to attain substantial yields of target peptides. The employment of such protective entities is paramount in peptide production for both investigative and therapeutic purposes.

Protein Engineering: Leveraging N-α-[2-(4-Biphenyl)isopropyloxycarbonyl]-N-ω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine in protein engineering empowers scientists to precisely tailor protein sites. Through the strategic integration of this compound, researchers can delve deeply into the intricate relationships between protein structure and function, achieving meticulous control over protein design. This facilitates the creation of proteins endowed with specific characteristics tailored for industrial or pharmaceutical applications.

Chemical Biology: A linchpin in chemical biology investigations, this compound serves as a cornerstone for synthesizing chemically altered versions of naturally occurring biomolecules. These analogs play a pivotal role in dissecting biological systems, deciphering enzyme mechanisms, and crafting inhibitors or activators. The utility of this compound is indispensable in propelling advancements in molecular biology and propelling drug discovery efforts.

Analytical Chemistry: Embraced in the realm of analytical chemistry, this compound excels in derivatizing amino acids and peptides, heightening detection sensitivity and enhancing resolution during chromatography or mass spectrometry analyses. This capability facilitates accurate quantification and characterization of biomolecules within intricate sample matrices, unveiling insights crucial for scientific investigations and biotechnological advancements.

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