82379-46-2

Upstream product

• 67729-36-6 Boc-Phe-O-COO-isoBu 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 13122-89-9 (S)-methyl 2-((S)-2-(tert-butoxycarbonylamino)-3-phenylpropanamido)-3-phenylpropanoate 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 40099-25-0 Boc-Phe-Phe-NH-NH₂ 

Downstream Products

• 83860-21-3 HCl*H-Phe-gPhe-mGly-Leu-Met-NH₂ 
• 82379-39-3 pGlu-Phe-gPhe-mGly-Leu-Met-NH₂ 
• 82379-49-5 Boc-Phe-gPhe-mGly-Leu-Met-NH₂ 
• 82379-48-4 N-malonyl-N'-<(tert-butoxycarbonyl)-L-phenylalanyl>-1,1-dimethylamino-2-phenylethane 
• 77367-58-9 Boc-Gln-Phe-Phe-Sar-Leu-Met-NH₂ 
• 82379-47-3 [(S)-1-((R)-1-Isocyanato-2-phenyl-ethylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester 
• 111610-72-1 Boc-Phe-Phe-Sar-Leu-Met-NH₂ 

Relevant academic research and scientific papers

SYNTHESIS OF DEHYDROPHENYLALANINE-CONTAINING ANALOGS OF 6-11 FRAGMENT OF SUBSTANCE P ADDITIONALLY MODIFIED IN POSITION 9

Five analogs of 6-11 fragment of Substance P: H-Gln-Phe-Phe-Sar-Leu-Met-NH2, Glp-Δ Phe-Sar-Leu-Met-NH2, Glp-Phe-Δ Phe-Sar-Leu-Met-NH2, Glp-Δ Phe-Phe-His-Leu-Met-NH2 and Glp-Phe-Δ Phe-His-Leu-Met-NH2 have been synthesized by classical methods.Except the fi

Synthesis of partially modified retro-inverso substance P analogues and their biological activity

Partial retro-inverso modification of a single peptide bond was applied to pGlu-Phe-Phe-Gly-Leu-Met-NH2 (I), a C-terminal hexapeptide analogue of the neuropeptide substance P. Two analogues with reversed peptide bonds, between the pGlu-Phe and