101624-82-2

Upstream product

• 1080-06-4 L-Tyr-OMe 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 19669-38-6 tert-butyl (2S)-2-{[(2S)-3-(4-hydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]carbamoyl}pyrrolidine-1-carboxylate 

Downstream Products

• 852333-15-4 Boc-Ile-Pro-Pro-Tyr-OMe 
• 937172-20-8 C₂₆H₃₄N₄O₈ 
• 1240383-94-1 tert-butoxycarbonyl-L-phenylalanyl-L-prolyl-L-prolyl-L-tyrosine methyl ester 
• 852333-18-7 Boc-Ile-Pro-Pro-Tyr-Val-Pro-Leu-Ile-OMe 
• 874337-86-7 Boc-Ile-Pro-Pro-Tyr-OH 

Relevant academic research and scientific papers

METHOD FOR PREPARING PEPTIDES

The invention relates to a method for preparing peptides comprising the step of forming a peptide bond wherein at least one amino acid or peptide comprises a protecting group having a water-solubility enhancing group, and said forming of a peptide bond is achieved while an amino acid or a peptide is bound to a solid phase. The invention further relates to peptides comprising a protecting group having a water-solubility enhancing group being bound to the amino group and an activated or free carboxyl group.

METHOD FOR PREPARING PEPTIDES

The invention relates to a method for preparing peptides comprising the step of forming a peptide bond wherein the carboxyl group of a first amino acid or first peptide is activated and an amino group of the first activated amino acid or first peptide is protected by a protecting group having a water-solubility enhancing group and the activated carboxyl group of the first amino acid or first peptide is reacted with an amino group of a second amino acid or second peptide wherein said carboxyl group of the first amino acid or first peptide is activated in the absence of the second amino acid or second peptide. The invention further relates to peptides comprising a protecting group having a water-solubility enhancing group being bound to the amino group and an activated or free carboxyl group.

PREPARATION AND USE OF REACTIVE OXYGEN SPECIES SCAVENGER

A compound of Formula (I), pharmaceutically acceptable salts thereof, and individual enantiomers or diastereomers thereof are disclosed. Compositions and methods useful for treatment or suppression of diseases, developmental delays and symptoms related to

Total synthesis and antimicrobial activity of a natural cycloheptapeptide of marine origin

The present study deals with the first total synthesis of the proline-rich cyclopolypeptide stylisin 2 via a solution phase technique by coupling of the Boc-L-Pro-L-Ile-L-Pro-OH tripeptide unit with the L-Phe-L-Pro-L-Pro-L-Tyr-OMe tetrapeptide unit, follo

Synthetic studies on cyclic octapeptides: Yunnanin F and Hymenistatin

Two biologically active cyclic peptides, Yunnanin F 8 and Hymenistatin 16 were synthesized and the structures were established on the basis of analytical, IR, NMR and mass spectral data. The newly synthesized compounds were screened for their antimicrobia