160347-94-4 Usage
Uses
Used in Chemical Synthesis:
FMOC-N-OMEGA-NITRO-D-ARGININE is used as a selective modifying agent for arginine residues in proteins and peptides, facilitating the synthesis of complex molecules with specific functionalities.
Used in Bioconjugation Reactions:
In bioconjugation, FMOC-N-OMEGA-NITRO-D-ARGININE serves as a key component for attaching proteins and peptides to other biomolecules or surfaces, enabling the creation of novel bioconjugates for various applications.
Used in Peptide and Protein Modification:
FMOC-N-OMEGA-NITRO-D-ARGININE is utilized as a modification tool for altering the properties of peptides and proteins, such as stability, solubility, and reactivity, through the introduction of the nitro group and the FMOC protecting group.
Used in Research Applications:
In the field of research, FMOC-N-OMEGA-NITRO-D-ARGININE is employed as a chemical probe to study the role of arginine residues in biological systems and to explore the effects of modifications on protein function and interactions.
Used in Pharmaceutical Development:
FMOC-N-OMEGA-NITRO-D-ARGININE may be used in the development of new pharmaceuticals, where its ability to modify arginine residues could lead to the design of drugs with improved efficacy or selectivity.
Used in Chemical Biology:
In chemical biology, FMOC-N-OMEGA-NITRO-D-ARGININE is applied as a tool for investigating protein function and interactions, as well as for the development of biosensors and other bioanalytical tools that rely on the selective modification of arginine residues.
Check Digit Verification of cas no
The CAS Registry Mumber 160347-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,3,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160347-94:
(8*1)+(7*6)+(6*0)+(5*3)+(4*4)+(3*7)+(2*9)+(1*4)=124
124 % 10 = 4
So 160347-94-4 is a valid CAS Registry Number.
160347-94-4Relevant academic research and scientific papers
Solid-phase total synthesis and structure proof of callipeltin B
Krishnamoorthy, Ravi,Vazquez-Serrano, Leslie D.,Turk, Jeffrey A.,Kowalski, Jennifer A.,Benson, Alan G.,Breaux, Nneka T.,Lipton, Mark A.
, p. 15392 - 15393 (2007/10/03)
The cytotoxic, cyclic heptadepsipeptide, natural product callipeltin B was synthesized on a solid-phase support in 15% overall yield. Comparison of the 1H NMR spectra of three synthetic isomers with those of callipeltin B confirmed the configurational reassignment of its threonine residues as d-allothreonine and the assignment of the configuration of its β-methoxytyrosine residue as (2R,3R). Copyright
Synthesis of arginine-containing hydroxamate dipeptidomimetics
Seo, Jiwon,Silverman, Richard B.
, p. 4069 - 4073 (2007/10/03)
The syntheses of arginine-containing hydroxamates using various peptide coupling methods are described. Fmoc-Arg(NO2)-Cl prepared at low temperature did not undergo intramolecular δ-lactam formation and effectively provided desired hydroxamates
