105678-36-2

Upstream product

• 90282-69-2 N-(tert-Butyloxycarbonyl)-L-isoleucyl-glycinbenzylester 
• 1738-76-7 glycine benzyl ester p-toluenesulfonic acid salt 
• 16948-38-2 N-t-butoxycarbonyl-L-isoleucine p-nitrophenyl ester 
• 13139-16-7 N-(tert-butyloxycarbonyl)-L-isoleucine 
• 63366-76-7 (toluene-4-sulfonylamino)acetic acid benzyl ester 

Downstream Products

• 90282-71-6 N-(tert-Butyloxycarbonyl)-glycyl-L-isoleucyl-glycinbenzylester 
• 173928-87-5 Boc-Tyr(Bzl)-Ile-Gly-OBzl 
• 119439-57-5 C₄₉H₇₄N₁₄O₁₅ 
• 119439-66-6 C₂₁H₃₃N₇O₆*ClH 
• 119439-58-6 C₅₈H₉₇N₁₇O₁₆S 
• 105678-34-0 3-O-(2,3,4-Tri-O-acetyl-β-D-xylopyranosyl)-N-(fluorenylmethoxycarbonyl)-L-seryl-glycyl-L-isoleucyl-glycinbenzylester 
• 105678-38-4 N-(Fluorenylmethoxycarbonyl)-L-seryl-glycyl-L-isoleucyl-glycinbenzylester 
• 105678-35-1 3-O-(β-D-Xylopyranosyl)-L-seryl-glycyl-L-isoleucyl-glycin 
• 105678-37-3 [(2S,3S)-2-(2-Amino-acetylamino)-3-methyl-pentanoylamino]-acetic acid benzyl ester 
• 173928-89-7 Boc-Tyr(Bzl)-Ile-Gly-Ser-Arg(NO₂)-OBzl 
• 173928-88-6 Boc-Tyr(Bzl)-Ile-Gly-NHNH₂ 
• 504431-33-8 Boc-Gly-Ile-Gly-Val-Pro-ONp 
• 504431-30-5 Boc-Gly-Ile-Gly-Val-Pro-OBzl 
• 119460-20-7 C₂₆H₄₁N₇O₈ 

Relevant academic research and scientific papers

Functionalization of Sulfonamide-Containing Peptides through Late-Stage Palladium-Catalyzed C(sp3)-H Arylation

Bioactive peptides are emerging as promising candidates of clinic therapeutics. Here, we report a method for late-stage functionalization of sulfonamide-containing peptides through Pd-catalyzed C(sp3)-H arylation. In this protocol, the backbone

Hydrophobicity profile of amino acid residues: A differential scanning calorimetry and circular dichroism study of leucine and isoleucine co-polypeptides of the protein-based polymers of elastin

The inverse temperature transition of hydrophobic folding and assembly of a "host-guest" model system based on the elastin derived polypentapeptide, poly(VPGVG), is employed to determine the relative hydrophobicity of amino acid residues of proteins and p

Amino acids and peptides. XXVI. Laminin-related peptide poly(ethylene glycol) hybrids and their inhibitory effect on experimental metastasis

Laminin-related peptide poly(ethylene glycol) hybrid, Tyr-Ile-Gly-Ser- Arg-aminopoly(ethylene glycol) was prepared by the solution method and carboxylated poly(ethylene glycol)-Tyr-Ile-Gly-Ser-Arg was prepared by the solid phase method. Their inhibitory effects on experimental tumor metastasis were examined in mice. The inhibitory effect of Tyr-Ile-Gly-Ser-Arg was significantly potentiated by hybrid formation with poly(ethylene glycol) either at amino- or carboxyl terminals of the peptide. Of the hybrids, Tyr- Ile-Gly-Ser-Arg-amino(polyethylene glycol) 6000 hybrid exhibited about 10 times more potent anti-metastatic effect than the peptide itself. The inhibitory effect of a mixture of the carboxylated poly(ethylene glycol) hybrid and Arg-Gly-Asp-aminopoly(ethylene glycol) hybrid also exhibited an inhibitory effect.

ATRIOPEPTINS. II. SYNTHESIS OF N-TERMINAL FRAGMENTS

Peptides, corresponding to the N-terminal sequence in atriopeptins, were synthesized by classical methods of peptide chemistry in solutions.The obtained peptides were characterized by various physicochemical methods.The scheme and methods of the synthesis are discussed.

SYNTHESE EINES XYLOSE-HALTIGEN GLYCOPEPTIDES, DAS DIE AMINOSAEURE-SEQUENZ 4 BIS 7 DES NH2-TERMINUS DER PROTEIN-CORE-STRUCTUR DES RINDERHAUT-PROTODERMATAN-SULFATS ENTHAELT

The synthesis is described of α-β-D-xylopyranosyl-L-serylglycyl-L-isoleucyl-glycine (7), a glycopeptide containing the amino acid sequence of the protein core-structure of beef-skin protodermatan sulfate; coupling of N-protected O-XylpSer with protected GlyIleuGly followed by deprotection afforded 7.