58172-54-6

Upstream product

• 2131-00-2 leucyl-methionine amide hydrochloride 
• 3235-59-4 Boc-Gly-Leu-Met-NH₂ 
• 40297-96-9 H-Gly-Leu-Met-NH₂ hydrochloride 
• 42280-29-5 [(S)-2-tert-butoxycarbonylamino-3-phenylpropanoylamino]acetic acid benzyl ester 
• 25616-33-5 2-((2S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)acetic acid 
• 2280-68-4 N-tert-butoxycarbonyl-L-leucyl-L-methioninamide 
• 73148-98-8 Boc-Phe-Gly-Leu-Met-NH₂ 

Downstream Products

• 136138-77-7 {(S)-1-Benzyl-2-[(S)-1-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-hydroxy-ethyl}-carbamic acid tert-butyl ester 
• 160693-33-4 Boc-Asp(OBzl)-Phe-Gly-Leu-Met-NH₂ 
• 160693-34-5 Boc-Glu(OBzl)-Phe-Gly-Leu-Met-NH₂ 
• 55572-15-1 L-phenylalanyl-L-phenylalanylglycyl-L-leucyl-L-methionine carboxamide hydrochloride 
• 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 
• 160693-35-6 Boc-Glu(OMe)-Phe-Gly-Leu-Met-NH₂ 
• 64699-01-0 t-butyloxycarbonyl-glutamyl-phenylalanyl-phenylalanyl-glycyl-leucyl-methionine amide 
• 79775-20-5 6,(RS)-mPhe⁷>SP_6-11 
• 73148-99-9 N-t-Boc-Phe-Phe-Gly-Leu-Met-NH₂ 

Relevant academic research and scientific papers

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 The amino-acid residue of other selected places has also been replaced by Glu(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.