77659-14-4

Upstream product

• 77659-13-3 Z-L-Pro-L-Ser-L-Tyr-OMe 
• 24118-03-4 Z-L-Ser-L-Tyr-OMe 
• 85476-33-1 HBr*H-L-Ser-L-Tyr-OMe 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 3304-59-4 N-benzyloxycarbonyl-L-proline p-nitrophenyl ester 

Downstream Products

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

Relevant academic research and scientific papers

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

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