Fmoc-L-Arg(Me,Me)-OH(asymmetrical)

≥97%

Reagent Code: #187792
label
Alias N5-[(dimethylamino)iminomethyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-ornithine
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CAS Number 268564-10-9

science Other reagents with same CAS 268564-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 424.49 g/mol
Formula C₂₃H₂₈N₄O₄
badge Registry Numbers
MDL Number MFCD00672718
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in peptide synthesis to introduce a modified arginine residue with dimethylated guanidine group. The Fmoc group allows for solid-phase synthesis by providing orthogonal protection, while the asymmetrical dimethylation mimics natural post-translational modifications found in proteins. This modification is particularly useful in studying protein arginine methylation, which plays a key role in epigenetic regulation, signal transduction, and RNA processing. The compound helps in preparing methylated histone peptides for use in biochemical assays, enzyme studies, and inhibitor development targeting protein methyltransferases or demethylases. Its structure supports improved cellular uptake and stability in certain peptide-based drug designs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,650.00
inventory 250mg
10-20 days ฿8,870.00
inventory 1g
10-20 days ฿25,410.00
Fmoc-L-Arg(Me,Me)-OH(asymmetrical)
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Used in peptide synthesis to introduce a modified arginine residue with dimethylated guanidine group. The Fmoc group allows for solid-phase synthesis by providing orthogonal protection, while the asymmetrical dimethylation mimics natural post-translational modifications found in proteins. This modification is particularly useful in studying protein arginine methylation, which plays a key role in epigenetic regulation, signal transduction, and RNA processing. The compound helps in preparing methylated histone peptides for use in biochemical assays, enzyme studies, and inhibitor development targeting protein methyltransferases or demethylases. Its structure supports improved cellular uptake and stability in certain peptide-based drug designs.
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