103725-76-4

Upstream product

• 16652-75-8 L-isoleucine benzyl ester tosylate 
• 3392-10-7 tert-butoxycarbonyl-L-proline N-hydroxysuccinimide ester 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 103310-88-9 L-isoleucine benzyl ester hydrochloride 
• 883565-15-9 C₁₅H₂₅NO₅ 

Downstream Products

• 731779-67-2 TFA*Pro-Ile-OBzl 
• 731779-66-1 H-L-Pro-L-Ile-OBz 
• 103725-55-9 Boc-L-Pro-L-Phe-L-Pro-Gly-L-Pro-L-Ile-OBz 
• 766467-87-2 H-L-Pro-L-Phe-L-Pro-Gly-L-Pro-L-Ile-OBz 
• 77654-52-5 L-prolyl-L-phenylalanyl-L-prolylglycyl-L-prolyl-L-isoleucine 

Relevant academic research and scientific papers

Synthesis of Pro-Pro-Ile, a corticoliberin fragment, labeled with tritium in proline unit

Boc-δ3Pro-Pro-Ile-OBzl and Boc-Pro-δ3Pro- Ile-OBzl were synthesized. Tritium-labeled Pro-Pro-Ile was prepared by their hydrogenation in a tritium atmosphere in the presence of a catalyst. In the reduction of Boc-δ3Pro-Pro-Ile-OBzl and Boc-Pro- δ3Pro-Ile-OBzl, elimination of the Bzl protective group occurs faster than hydrogenation of the 3,4-dehydroproline residue (benzene and dioxane were used as solvents). The resulting Boc-δ3Pro-Pro-Ile-OH and Boc-Pro-δ3Pro-Ile-OH are poorly soluble in aprotic solvents, which accounts for the low yield of the desired tritium-labeled peptides. Pleiades Publishing, Inc., 2010.

Synthesis and biological evaluation of vinca alkaloids and phomopsin hybrids

Ten hybrids of vinca alkaloids and phomopsin A have been synthesized by linking the octahydrophomopsin lateral chain to the tertiary amine of the cleavamine moiety of anhydrovinblastine (AVLB) and vinorelbine. These compounds have been elaborated in order

Structure of Halo-toxin Procedured by Phytopathogenic Bacterium, Pseudomonas syringae pv. mori

Halo-toxin was isolated from the incubated medium of Pseudomonas syringae pv. mori which causes halo bright disease against the leaves of mulberry trees.The structure of this compound was revealed to be Pro-Phe-Pro-Gly-Pro-Ile by spectroscopic means and a