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Product Information

Product Name
Na-Fmoc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine
Brand Name
Chem Impex
Product Number
00146
CAS
98930-01-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
3010428
IUPAC Name
(2S)-5-amino-(4-methoxy-2,3,6-trimethylphenyl)sulfonylaminomethylideneamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid
InChI Key
LKGHIEITYHYVED-SANMLTNESA-N
SMILES
CC1=CC(=C(C(=C1S(=O)(=O)NC(=NCCCC@@H(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)N)C)C)OC

Application

Na-Fmoc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.

Drug Development: Its unique structure aids in the design of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.

Bioconjugation: The compound can be used to attach peptides to various biomolecules, facilitating the development of targeted drug delivery systems and diagnostic agents.

Research in Biochemistry: It is valuable in studying protein interactions and functions, providing insights into cellular processes and disease mechanisms.

Custom Synthesis: Researchers can utilize this compound for tailored peptide sequences, enabling the exploration of specific biological pathways and therapeutic targets.

References Data Source From Pubchem

A Novel Chemoenzymatic Approach to Produce Cilengitide Using the Thioesterase Domain from Microcystis aeruginosa Microcystin Synthetase C

Publication Name: The Protein Journal
Publication Date: 2019-08-21
DOI: 10.1007/s10930-019-09864-1

The discovery, characterization and crystallographically determined binding mode of an FMOC-containing inhibitor of HIV-1 protease

Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 1997-07
DOI: 10.1016/s0968-0896(97)00078-3

Fmoc-Argω,ω′ (Boc)2-OH and Z-Argω,ω′ (Boc) 2-OH: New arginine derivatives for peptide synthesis

Publication Name: Peptides
Publication Date: 1992
DOI: 10.1007/978-94-011-2264-1_219

Acid labile protection of histidine and arginine in SPPS using Adpoc derivatives

Publication Name: Peptides 1990
Publication Date: 1991
DOI: 10.1007/978-94-011-3034-9_8

Synthesis and biological activities of rabbit corticostatin (rCS)

Publication Name: Peptides
Publication Date: 1990
DOI: 10.1007/978-94-010-9060-5_77