13585-98-3

Upstream product

• 3057-69-0 N-[(benzyloxy)carbonyl]-L-alanyl-L-alanyl-L-alanine methyl ester 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 35661-39-3 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine 
• 41036-19-5 L-alanyl-alanine methylester hydrochloride 
• 19794-10-6 (S)-methyl 2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)propanoate 
• 16012-70-7 benzyloxycarbonyl-L-alanyl-L-alanine 
• 76413-56-4 3-(N-benzyloxycarbonyl-L-alanyl)-1,3-thiazolidine-2-thione 
• 95930-17-9 L-Ala-L-Ala-OH*HBr 
• 13883-50-6 Z-(L-Ala)3-O-t-Bu 

Downstream Products

• 73974-15-9 6-(Benzyloxycarbonyl-alanyl-alanyl-alanylamino)penicillansaeure 
• 90427-62-6 Z-Ala₂-Ala-AlaCH₃ 
• 88576-79-8 Z-Ala₂-Ala-PheCH₃ 
• 89595-83-5 Z-Ala₃-PheCH₂Cl 
• 5874-90-8 L-ala-L-ala-L-ala 
• 90427-69-3 Glp-Ala₃-PheCH₃ 
• 90427-67-1 Ac-Ala₃-PheCH₃ 
• 95930-19-1 N^α-benzyloxycarbonyl-N^ε-t-butoxycarbonyl-L-lysyl-L-alanyl-L-alanyl-L-alanine 

Relevant academic research and scientific papers

Methyl to trifluoromethyl substitution as a strategy to increase the membrane permeability of short peptides

Here, we investigated the effect of CH3to CF3substitution on the membrane permeability of peptides. We synthesized a series of peptides with CF3groups and corresponding nonfluorinated peptides and measured the membrane per

Haem-Peptide Complexes. Synthesis and Stereoselctive Oxidations by Deuterohaemin-L-Phenylalanyl-poly-L-Alanine Complexes

Deuterohaemin-L-histidine methyl ester-peptide complexes have been obtained by covalently linking L-histidine methyl ester and the peptides Ala-Ala-Phe-Ala-Ala-Ala-Ala-Ala-Ala-Ala (compound 3) or Ala-Ala-Ala-Phe-Ala-Ala-Ala-Ala-Ala-Ala (compound 4) on the

Peptide-bond Formation, Chemoselective Acylation of Amino Acids, and Crosslinking Reaction between Amino Acids Utilizing a Functional Five-membered Heterocycle, 1,3-Thiazolidine-2-thione

The monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thiones has been extended to the peptide-bond formation, the chemoselective acylation of amino acids having multifunctional groups, and the crosslinking reaction between amino acids.

Thermitase - A Thermostable Serine Protease. II. Synthesis of Substrate Analogous Peptide Chloromethyl Ketones as Irreversibly Acting Inhibitors

The preparation of dipeptide to pentapeptide chloromethyl ketones of alanine with variation of the amino acid in the P1 and P2 position of the peptides is described.The synthesis is performed by fragment condensation of N-acylated amino acids or peptides with the unprotected chloromethyl ketone derivatives of amino acids and peptides, respectively.Some examples of enzyme inactivation by peptide chloromethyl ketones are discussed.