73148-98-8

Basic information

• Product Name: L-Methioninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanylglycyl-L-leucyl-
• CAS NO: 73148-98-8
• Molecular Formula: C27H43N5O6S
• Molecular Weight: 565.734
• Mol File: 73148-98-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: L-Methioninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanylglycyl-L-leucyl-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Methioninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanylglycyl-L-leucyl-(73148-98-8)
• EPA Substance Registry System: L-Methioninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanylglycyl-L-leucyl-(73148-98-8)

Safety Data

• Hazardous Substances Data: 73148-98-8(Hazardous Substances Data)

Upstream product

• 2131-00-2 leucyl-methionine amide hydrochloride 
• 3235-59-4 Boc-Gly-Leu-Met-NH₂ 
• 42280-29-5 [(S)-2-tert-butoxycarbonylamino-3-phenylpropanoylamino]acetic acid benzyl ester 
• 2280-68-4 N-tert-butoxycarbonyl-L-leucyl-L-methioninamide 
• 25616-33-5 2-((2S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)acetic acid 
• 40297-96-9 H-Gly-Leu-Met-NH₂ hydrochloride 
• 50903-54-3 N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine pentafluorophenyl ester 
• 7625-57-2 methyl 2-((2S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)acetate 
• 92232-98-9 S-leucyl-S-methionine amide hydrobromide 
• 16217-56-4 (S,S)-leucinylmethionine amide 

Downstream Products

• 58172-54-6 H-Phe-Gly-Leu-Met-NH₂ hydrochloride 
• 55572-15-1 L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-L-methionine carboxamide hydrochloride 
• 73148-99-9 N-t-Boc-Phe-Phe-Gly-Leu-Met-NH₂ 
• 160693-41-4 Boc-Orn(Boc)-Glu(OBzl)-Phe-Gly-Leu-Met-NH₂ 
• 160693-40-3 Boc-Orn(Boc)-Asp(OBzl)-Phe-Gly-Leu-Met-NH₂ 
• 160693-42-5 Boc-Orn(Boc)-Glu(OMe)-Phe-Gly-Leu-Met-NH₂ 
• 160693-34-5 Boc-Glu(OBzl)-Phe-Gly-Leu-Met-NH₂ 
• 160693-33-4 Boc-Asp(OBzl)-Phe-Gly-Leu-Met-NH₂ 
• 160693-35-6 Boc-Glu(OMe)-Phe-Gly-Leu-Met-NH₂ 

Relevant articles and documents

Synthesis of substance-P C-terminal hexapeptide analogues and their biological activity. Analogues with antagonistic activity without containing D-amino acids

Analogues of the C-terminal hexapeptide of substance P have been synthesized in which each amino-acid residue was replaced by the bulky and strong lipophilic residue Asp(OBzl). The amino-acid residue of other selected places has also been replaced by Glu(

DEHYDROPHENYLALANINE ANALOGS OF 6-11 FRAGMENT OF SUBSTANCE P

Two dehydro analogs of 6-11 fragment of Substance P: p-Glu-Phe-Δ Phe-Gly-Leu-MetNH2 and p-Glu-Δ Phe-Phe-Gly-Leu-MetNH2 have been synthesized by solution methodology.Both compounds are biologically active on blood pressure in rats.

Model Studies on Papain-Catalyzed Peptide Synthesis in a Biphasic Aqueous-Organic System

Several model peptides have been synthesized enzymatically using papain as a catalyst in biphasic aqueous-organic systems.The effect of different cosolvents, pH, buffer concentration, and reaction time on the papain-catalyzed synthesis was examined.A comp