53734-02-4

Upstream product

• 53195-68-9 N^α-BOC-N^ε-Z-Lys-Pro-OMe 
• 56-87-1 L-lysine 
• 84890-96-0 C₂₄H₃₆N₂O₈ 
• 2389-45-9 Boc-Lys(Z)-OH 
• 2133-40-6 L-proline methyl ester monohydrochloride 
• 2389-46-0 N-α-tert-butyloxycarbonyl-N-ε-benzyloxycarbonyl-lysine p-nitrophenyl ester 
• 1155-64-2 N₆-[(benzyloxy)carbonyl]-L-lysine 
• 2577-48-2 methyl (2S)-pyrrolidine carboxylate 

Downstream Products

• 78314-58-6 Boc-Pro-Lys(Z)-Pro-OCH₃ 
• 85574-68-1 Boc-Sar-Lys(Z)-Pro-OMe 
• 78314-59-7 Z₃Arg-Pro-Lys(Z)-Pro-OMe 
• 78314-62-2 Z₃-Arg-Pro-Lys(Z)-Pro-OH 
• 78326-84-8 Cyclo 
• 85574-66-9 Cyclo 
• 85574-59-0 Boc-Trp(CHO)-Sar-Sar-Lys(Z)-Pro-OSu 
• 85574-58-9 Boc-Trp(CHO)-Sar-Sar-Lys(Z)-Pro-OH 
• 85574-57-8 Cyclo 
• 85574-70-5 Boc-Sar-Sar-Lys(Z)-Pro-OMe 
• 85574-71-6 Boc-Sar-Sar-Lys(Z)-Pro-OH 
• 85574-72-7 Sar-Sar-Lys(Z)-Pro-OH 
• 790613-73-9 H-Sar-Lys(Z)-Pro-OMe 

Relevant academic research and scientific papers

Cyclodipeptide c(Orn-Pro) Conjugate with 4-Ethylpiperic Acid Abrogates Cancer Cell Metastasis through Modulating MDM2

The present work describes the synthesis, characterization, and anticancer properties of c(Lys-Pro), P1; c(Orn-Pro), P2; and conjugates PA-c(Lys-Pro), C1; PA-c(Orn-Pro), C2; EPA-c(Lys-Pro), C3; and EPA-c(Orn-Pro), C4. Among all, conjugate C4 displays pote

Intramolecular Transfer of Excitation Energy, Complexation with Metal Ions, and Interactions with Liposomes of Cycloε-dansyllysyl-prolyl>

A cyclic pentapeptide containing an energy donor group and an energy acceptor group within the molecule, cyclo, was synthesized.Its conformation, complexation with metal ions, intramolecular energy transfer, and interaction with

INVESTIGATION ON PEPTIDE SYNTHESIS BY FRAGMENT CONDENSATION. PART I. SYNTHESIS OF C1 - C4 FRAGMENT OF SUBSTANCE P IN SOLUTION AND BY THE SOLID PHASE METHOD

The synthesis of protected tetrapeptide Z3-Arg-Pro-Lys(Z)-Pro-OH corresponding to C1 - C4 fragment of substance P in solution and by the solid phase method has been elaborated.