82379-40-6

Upstream product

• 32159-21-0 Cbz-L-pGlu-OH 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 112335-67-8 N-benzyloxycarbonyl-α-pyroglutamyl-L-leucyl-O^β-benzyl-L-threonyl-L-phenylalanine methyl ester 
• 130619-29-3 N-benzyloxycarbonyl-L-pyro-glutamyl-L-valyl-L-asparginyl-L-phenylalanyl-L-seryl-L-prolyl-L-asparginyl-L-tryptophane amide 
• 82379-41-7 (S)-2-Azidocarbonyl-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 66488-70-8 N,N'-Bis-'L'-5-aminopyrrolidin-2-one 
• 66488-77-5 (S)-2-Isocyanato-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 153870-06-5 (2S,5S)-2-Hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-pyrrolidine-1-carboxylic acid benzyl ester 
• 153870-09-8 (S)-1-(benzyloxycarbonyl)-5-[(tert-butyldimethylsilyl)oxymethyl]-2-pyrrolidinone 
• 83444-03-5 Z-Pyr-Gly-Pro-OH CHA Salt 
• 93208-51-6 periplanetin CC-1 
• 93240-39-2 periplanetin CC-2 
• 112335-71-4 (S)-5-Oxo-pyrrolidine-2-carboxylic acid {(S)-1-[(1S,2R)-1-((S)-1-hydrazinocarbonyl-2-phenyl-ethylcarbamoyl)-2-hydroxy-propylcarbamoyl]-3-methyl-butyl}-amide 

Relevant academic research and scientific papers

Pyrrolidine based analogs of 3′-deoxythymidine

Pyrrolidine based analogs of 3′-deoxythymidine la,b and 2a,b have been prepared via N-acyliminium ion intermediates 3 and 4.

Periplanetin CC-1 Myotropic Peptide from corpora cardiaca of Cockroach Periplaneta americana L. New Synthesis and Biological Studies

Periplanetin CC-1 (Glu-Val-Asn-Phe-Ser-Pro-Asn-Trp-NH2) (1) neuropeptide from corpora cardiaca of the American cocroach Periplaneta americana has been synthesized by the liquid-phase method.In biological studies on the larvae of yellow mealworm, Tenebrio

Synthesis and Biological Investigations of Hyperglycaemic Peptide-Periplanetin CC-2 from corpora cardiaca of Cockroach Periplaneta americana L.

Periplanetin CC-2 (Glu-Leu-Thr-Phe-Thr-Pro-Asn-Trp-NH2) (1) neuropeptide from corpora cardiaca of the American cocroach Periplaneta americana has been synthesized by the liquid-phase method.In biological investigations into the larvae of yellow mealworm-

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