41446-15-5

Upstream product

• 26582-86-5 benzyl (1S)-2-hydrazino-1-(hydroxymethyl)-2-oxoethylcarbamate 

Downstream Products

• 117864-50-3 N-benzyloxycarbonyl-L-seryl=>glycyl=>glycyl=>glycine ethyl ester 
• 114795-73-2 N-[N-(N-benzyloxycarbonyl-L-seryl)-L-methionyl]-L-glutamic acid 
• 55325-57-0 N-(N-benzyloxycarbonyl-L-seryl)-D-valine methyl ester 
• 14614-22-3 Z-Ser-Met-OMe 
• 47662-66-8 benzyloxycarbonylseryl-glycyl-glutamic acid 
• 1738-94-9 N-[N-(N-benzyloxycarbonyl-L-seryl)-glycyl]-glycine benzyl ester 
• 25529-46-8 N-(N-benzyloxycarbonyl-L-seryl)-L-phenylalanine amide 
• 1676-77-3 Z-L-Ser-Gly-OMe 
• 110157-28-3 Z-L-Ser-L-His-OMe 
• 3236-13-3 Z-Ser-Lys(Boc)-OH 
• 89762-51-6 Benzyloxycarbonyl-S-seryl-S-phenylalanyl-S-prolin-methylester 
• 111334-70-4 Z-Ser-Ser-Thr-Ser-OMe 
• 73167-79-0 Z-Ser-Thr-Ser-OMe 
• 75893-37-7 Z-Ser-Ser-NHNHBoc 

Relevant academic research and scientific papers

Amino acids and peptides. XXXVII. Synthesis of stereoisomeric nonapeptides corresponding to sequence 41-49 of eglin c and examination of their inhibitory activity against human leukocyte cathepsin G and α-chymotrypsin

A nonapeptide, H-Ser-Pro-Val-Thr-Leu-Asp-Leu-Arg-Tyr-OH, corresponding to sequence 41-49 of eglin c inhibited leukocyte cathepsin G and α-chymotrypsin with K(i) values of 2.2 x 10-5 and 7.2 x 10-6 M, respectively, although eglin c it

Amino acids and peptides. XXV. Application of newly developed beta-1- and beta-2-adamantylaspartates to peptide synthesis by solid phase and conventional solution methods.

Newly developed beta-1- and beta-2-adamantylaspartates [H-Asp(O-1-Ada)-OH and H-Asp(O-2-Ada)-OH] were applied to the synthesis of a C-terminal octapeptide of the beta-subunit of human chorionic gonadotropin (hCG) by a conventional solution method and a he

Synthesis of PHI (Peptide Histidine Isoleucine) and Related Peptides and Immunochemical Confirmation of Amino Acid Residue in Position 24 of PHI with use of the Synthetic Peptides

An immunochemical approach, using synthetic peptides, was employed to establish the nature of residue 24 in the amino acid sequence of PHI (peptide histidine isoleucine).PHI(20-27) and 24>-PHI(20-27) were synthesized by conventional solutio

HUMAN CHORIONIC GONADOTROPIN. IV. SYNTHESIS OF A HEXADECAPEPTIDE CORRESPONDING TO THE C-TERMINAL SEQUENCE 130-145 OF THE β-SUBUNIT OF HUMAN CHORIONIC GONADOTROPIN (hCG)

The hexadecapeptide corresponding to sequence 130-145 of the β-subunit of human chorionic gonadotropin (hCG) according to the amino acid sequence proposed by Morgan et. al. was synthesized by successive azide condensation of 4 peptide fragments, followed

Amino Acids and Peptides. VI. Curtius Rearrangement of Acyl Amino Acid and Peptide Azides and Reactivity of the Isocyanates

Studies on the rate of Curtius rearrangement of acyl amino acid and peptide azides were carried out by means of IR (infrared) spectrophotometry at 25 deg.It was found that Z-Gly-N3 and Z-Pro-N3 were more stable than the other acyl amino acid azides.The re