64152-92-7

Basic information

• Product Name: L-Leucine, N-[N-[N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-L-tyrosyl]-D-alanyl]-, methyl ester
• CAS NO: 64152-92-7
• Molecular Formula: C30H40N4O9
• Molecular Weight: 600.669
• Mol File: 64152-92-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-Leucine, N-[N-[N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-L-tyrosyl]-D-alanyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Leucine, N-[N-[N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-L-tyrosyl]-D-alanyl]-, methyl ester(64152-92-7)
• EPA Substance Registry System: L-Leucine, N-[N-[N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-L-tyrosyl]-D-alanyl]-, methyl ester(64152-92-7)

Safety Data

• Hazardous Substances Data: 64152-92-7(Hazardous Substances Data)

Upstream product

• 55610-27-0 Z-L-Ser-L-Tyr-N₂H₃ 
• 13673-57-9 N-(benzyloxycarbonyl)-L-serine pentachlorophenyl ester 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 24118-03-4 Z-L-Ser-L-Tyr-OMe 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 27167-66-4 Z-D-Ala-L-Leu-OMe 
• 58111-84-5 Z-L-Ser-L-Tyr-N₃ 
• 85476-34-2 HBr*H-D-Ala-L-Leu-OMe 
• 67503-95-1 H-D-Ala-Leu-OMe 

Downstream Products

• 87163-40-4 H-D-Pro-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt 
• 87163-42-6 BOC-Phe-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt 
• 111973-90-1 Z-D-Pro-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt 
• 111945-56-3 BOC-pGlu-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt 
• 111945-54-1 Z-Ser-Tyr-D-Ala-Leu-Arg(NO₂)-Pro-NHEt 
• 87163-41-5 pGlu-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt 
• 87163-39-1 H-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt 
• 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 
• 77659-17-7 Z-Pro-Ser-Tyr-D-Ala-Leu-(O₂N)Arg-Pro-Gly-NH₂ 
• 111945-52-9 Z-Ser-Tyr-D-Ala-Leu-N₂H₃ 

Relevant articles and documents

SYNTHESIS AND INVESTIGATION OF THE BIOLOGICAL ACTIVITY OF SHORTENED ANALOGUES OF LULIBERIN

Five new luliberin analogues with shortened amino acid sequences have been synthesized.The different variants for obtaining the compounds under consideration are discussed.In an investigation of the biological activities of the analogues it was shown that

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