2418-67-9

Usage

InChI:InChI=1/C8H17N5O3/c9-5(2-1-3-12-8(10)11)7(16)13-4-6(14)15/h5H,1-4,9H2,(H,13,16)(H,14,15)(H4,10,11,12)/t5-/m0/s1

Upstream product

• 109454-27-5 N-[N^ω-nitro-N^α-(4-nitro-benzyloxycarbonyl)-L-arginyl]-glycine ethyl ester 
• 183659-61-2 N^ω-nitro-N^α-(4-nitro-benzyloxycarbonyl)-L-arginine 
• 2149-70-4 N-nitro-L-arginine 
• 14611-34-8 N^α,N^δ,N^ω-tris(benzyloxycarbonyl)-L-arginine 
• 2304-98-5 N₅-[imino(nitroamino)methyl]-N₂-[(phenylmethoxy)carbonyl]-L-ornithine 
• 21466-91-1 N^α-benzyloxycarbonyl-N^G-nitroarginylglycine p-nitrobenzyl ester 
• 21466-92-2 ((S)-2-benzyloxycarbonylamino-5-(nitroguanidino)pentanamido)ethanoic acid 
• 2418-80-6 N^ω-Nitro-L-arginyl-glycin 
• 69538-48-3 N^α,N^G,N^G-tribenzyloxycarbonylarginylglycine benzyl ester 
• 132515-75-4 N-[N^ω-nitro-N^α-(4-nitro-benzyloxycarbonyl)-L-arginyl]-glycine 
• 21466-92-2 N^α-benzyloxycarbonyl-N^G-nitroarginylglycine 
• 24127-10-4 N^α-benzyloxycarbonyl-N^G-nitroarginylglycine benzyl ester 
• 5085-27-8 Z-Arg(Z)-Gly-OMe 
• 74-79-3 L-arginine 

Downstream Products

• 74-79-3 L-arginine 
• 56-40-6 glycine 

Relevant academic research and scientific papers

A novel L-amino acid ligase from Bacillus subtilis NBRC3134, a microorganism producing peptide-antibiotic rhizocticin

L-Amino acid ligase catalyzes the formation of an α-peptide bond from unprotected L-amino acids in an ATP-dependent manner, and this enzyme is very useful in efficient peptide production. We performed enzyme purification to obtain a novel L-amino acid lig

Deblocking of peptides with proton donors

A series of model di- and tripeptides were synthesized, and they were deblocked with ammonium formate and cyclohexene in the presence of a palladium catalyst.It was shown that the deblocking of the peptides containing nitroarginine takes place readily and