77659-13-3

Upstream product

• 3304-59-4 N-benzyloxycarbonyl-L-proline p-nitrophenyl ester 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 24118-03-4 Z-L-Ser-L-Tyr-OMe 
• 85476-33-1 HBr*H-L-Ser-L-Tyr-OMe 

Downstream Products

• 77659-15-5 Z-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-OMe 
• 77659-16-6 Z-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-N₂H₃ 
• 85476-29-5 Z-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg(NO₂)-L-Pro-NHEt 
• 85476-31-9 Z-D-Phe-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg-L-Pro-NHEt 
• 85476-30-8 H-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg-L-Pro-NHEt 
• 77659-17-7 Z-Pro-Ser-Tyr-D-Ala-Leu-(O₂N)Arg-Pro-Gly-NH₂ 
• 77659-14-4 Hydrazide of benzyoxycarbonyl-L-prolyl-L-seryl-L-tyrosine 

Relevant academic research and scientific papers

SYNTHESIS OF BIOLOGICALLY ACTIVE ANALOGS OF LULIBERIN WITH SHORTENED AMINO ACID SEQUENCES

Two new analogs of the releasing factor of the luteinizing hormone with shortened amino acid sequences have been synthesized by the methods of classical peptide chemistry.The influence of the preparations on the action of chorionic gonadotropin and on the

SYNTHESIS OF 3(NH2); Pro3; D-Ala6>- and 2(NO2); Pro3; D-Ala6>LULIBERINS

In order to study the influence of substituents of the aromatic ring of D-phenylalanine on the inhibiting capacity of luliberian analogs, we have synthesized two new analogs: 2; Pro3; D-Ala6>- and