55572-15-1

Basic information

• Product Name: L-Methioninamide, L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-, monohydrochloride
• CAS NO: 55572-15-1
• Molecular Formula: C31H44N6O5S.ClH
• Molecular Weight: 649.255
• Mol File: 55572-15-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-Methioninamide, L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-, monohydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: L-Methioninamide, L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-, monohydrochloride(55572-15-1)
• EPA Substance Registry System: L-Methioninamide, L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-, monohydrochloride(55572-15-1)

Safety Data

• Hazardous Substances Data: 55572-15-1(Hazardous Substances Data)

Upstream product

• 73148-98-8 Boc-Phe-Gly-Leu-Met-NH₂ 
• 58172-54-6 H-Phe-Gly-Leu-Met-NH₂ hydrochloride 
• 40297-96-9 H-Gly-Leu-Met-NH₂ hydrochloride 
• 3235-59-4 Boc-Gly-Leu-Met-NH₂ 
• 62307-54-4 Boc-Phe-Phe-Gly-OEt 
• 41041-68-3 L-phenylalanyl-glycine ethyl ester*HCl 
• 30189-51-6 ethyl (N-tert-butoxycarbonyl-L-phenylalanyl)glycinate 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 2280-69-5 Boc-Leu-Met-OMe 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 64698-97-1 Boc-Phe-Phe-Gly-OBzl 
• 82816-76-0 N-tert-butoxycarbonyl-L-phenylalanine-L-phenylalanine-glycine 
• 2131-00-2 leucyl-methionine amide hydrochloride 
• 2280-68-4 N-tert-butoxycarbonyl-L-leucyl-L-methioninamide 

Downstream Products

• 97721-55-6 C₄₃H₆₄N₁₀O₉S₃*ClH 
• 97721-56-7 N-t-Boc-(S-Acm)Cys-(S-Acm)Cys-Phe-Phe-Gly-Leu-Met-NH₂ 
• 103945-75-1 H-His-Phe-Phe-Gly-Leu-Met-NH₂*2HBr 
• 97731-61-8 ((4R,7R)-4-{(S)-1-[(S)-1-({[(S)-1-((S)-1-Carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-phenyl-ethylcarbamoyl}-6-oxo-[1,2,5]dithiazocan-7-yl)-carbamic acid tert-butyl ester 
• 103945-74-0 Z-His-Phe-Phe-Gly-Leu-Met-NH₂ 
• 97731-60-7 (4R,7R)-7-Amino-6-oxo-[1,2,5]dithiazocane-4-carboxylic acid {(S)-1-[(S)-1-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-phenyl-ethyl}-amide 
• 160693-43-6 Boc-Asp(OBzl)-Phe-Phe-Gly-Leu-Met-NH₂ 
• 103929-13-1 4-((S)-2-Benzyloxycarbonylamino-2-{(S)-1-[(S)-1-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-phenyl-ethylcarbamoyl}-ethyl)-imidazole-1-carboxylic acid benzyl ester 
• 108744-23-6 α-(tert-butyloxycarbonyl)-α-aspartyl<8-<4-<<<<(aminoethyl)amino>carbonyl>methyl>oxy>phenyl>-1,3-dipropylxanthin-4.2-yl>>-L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-L-methionine amide 

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(

'Rapid synthesis' of substance P

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