2566-20-3

Usage

Chemical Properties

White powder

InChI:InChI=1/C14H17N3O6/c18-11(16-8-13(20)21)6-15-12(19)7-17-14(22)23-9-10-4-2-1-3-5-10/h1-5H,6-9H2,(H,15,19)(H,16,18)(H,17,22)(H,20,21)

Upstream product

• 556-50-3 glycylglycine 
• 7444-16-8 N-(benzyloxycarbonyl)glycine anhydride 
• 81093-03-0 (N-benzyloxycarbonyl-glycylmercapto)-acetic acid 
• 109590-23-0 2-(N-benzyloxycarbonyl-glycylmercapto)-benzoic acid 
• 556-33-2 glycine-glycine-glycine 
• 501-53-1 benzyl chloroformate 
• 80681-01-2 [2-Oxo-2-(2-thioxo-thiazolidin-3-yl)-ethyl]-carbamic acid benzyl ester 
• 13443-59-9 N-benzyloxycarbonylglycylglycylglycyne methyl ester 
• 16295-43-5 benzyloxycarbonyl-triglycyl-L-leucyl-glycine 
• 106-57-0 Glycine anhydride 
• 15050-24-5 N-(benzyloxycarbonyl)glycyl chloride 
• 3005-87-6 Z-Gly-Gly-OEt 
• 2503-35-7 N-benzyloxycarbonyl-glycyl=>glycyl=>-glycine ethyl ester 
• 2566-19-0 CbzGlyGly 

Downstream Products

• 7770-50-5 N-benzyloxycarbonylglycylglycylglycylglycine 
• 4811-37-4 N-benzyloxycarbonyl-glycyl=>glycyl=>glycyl=>-glycine ethyl ester 
• 20228-72-2 Benzyloxycarbonyl-glycyl-glycyl-glycyl-glycyl-glycin 
• 116929-50-1 N⁶-benzyloxycarbonyl-N²-{N-[N-(N-benzyloxycarbonyl-glycyl)-glycyl]-glycyl}-L-lysine methyl ester 
• 168465-28-9 (S)-2-{2-[2-(2-Benzyloxycarbonylamino-acetylamino)-acetylamino]-acetylamino}-pentanedioic acid di-tert-butyl ester 
• 556-50-3 glycylglycine 
• 2566-19-0 CbzGlyGly 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 548783-75-1 Z-Gly-Gly-Gly-NH-1-adamantane 
• 714293-34-2 benzyloxycarbonyldiglicylglycinamide-N'-ethyl-2-N'-carbomoyl-(3,7-dimethoxy-2-naphthalene) 
• 556-33-2 glycine-glycine-glycine 
• 97347-10-9 N-(benzyloxycarbonyl)glycylglycylglycyl-L-serine methyl ester 
• 33374-78-6 N-benzyloxycarbonylglycylglycylglycyl-D,L-phenylalanine methyl ester 
• 21313-39-3 N-benzyloxycarbonylglycylglycylglycine pentachlorophenyl ester 

Relevant academic research and scientific papers

Second generation specific-enzyme-activated rotaxane propeptides

A [2]rotaxane, in which the peptidic axle is protected from degradation by the macrocyclic sheath and terminated with a novel glycosidase-cleavable stopper, is rendered water-soluble by derivatisation with tetra(ethylene glycol) (TetEG) or glucosylated te

1:3 Complex between β-cyclodextrin and dendrimer with three branches involving four glycine and one adamantyl group

The first-generation dendrimer, benzene-sym-tris-N,N,N-carbonyltriglycylglycine N′-1-adamantylamide, was synthesized by a modification of a described procedure. Its complexation with α-, β- and γ-cyclodextrins was studied by NMR. The complexation induced

2-amino-6,7-dihydroxy-4-thiaheptanoic acid derivatives, production and use thereof

A compound of the formula: STR1 wherein each of R1 and R2 is hydrogen or aliphatic acyl, A is amino which may be protected, X is an amino acid sequence consisting of 1 to 10 amino acid residues which contain at least one amino acid r

Synthesis of N-glycopeptides and a neoglycoprotein.

O-(alpha-D-Glucopyranosyl)-(1----6)-O-beta-D-glucopyranosyl-(1----6)-1-N -(glycylglycylglycyl-L-seryl-L-leucyl-L-glutam-5-oyl)-alpha- D -glucopyranosylamine has been prepared, as a model of a derivative possibly present in the glomerular basement membrane

3-AMINOACYL-TETRAHYDROTHIAZOLE-2-THIONE AS AN ACTIVE AMIDE FOR PEPTIDE SYNTHESIS (I)

3-Aminoacyl-tetrahydrothiazole-2-thione can be used as an active amide for peptide synthesis.A series of peptides have been synthesized with satisfactory yields by this methods.