85476-31-9

Upstream product

• 85476-30-8 H-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg-L-Pro-NHEt 
• 27167-66-4 Z-D-Ala-L-Leu-OMe 
• 24118-03-4 Z-L-Ser-L-Tyr-OMe 
• 1148-11-4 N-Benzyloxycarbonyl-L-proline 
• 51536-91-5 Z-L-Arg(NO₂)-L-Pro-NHEt 
• 85476-34-2 HBr*H-D-Ala-L-Leu-OMe 
• 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 
• 57866-94-1 HBr*H-L-Arg(NO₂)-L-Pro-NHEt 
• 77659-14-4 Hydrazide of benzyoxycarbonyl-L-prolyl-L-seryl-L-tyrosine 
• 77659-13-3 Z-L-Pro-L-Ser-L-Tyr-OMe 
• 85476-33-1 HBr*H-L-Ser-L-Tyr-OMe 
• 85476-32-0 HBr*H-L-Pro-NHEt 

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