41271-84-5

Upstream product

• 1668-10-6 glycinamide hydrochloride 
• 50587-00-3 N^α-Benzyloxycarbonyl-L-leucyl-N^G-nitro-L-arginyl-L-proline 
• 2304-98-5 N₅-[imino(nitroamino)methyl]-N₂-[(phenylmethoxy)carbonyl]-L-ornithine 
• 3268-81-3 N^α-Benzyloxycarbonyl-N^G-nitro-L-arginyl-L-proline Methyl Ester 
• 49761-07-1 N^G-Nitro-L-arginyl-L-proline Methyl Ester Hydrobromide 
• 50700-69-1 N^α-Benzyloxycarbonyl-L-leucyl-N^G-nitro-L-arginyl-L-proline Methyl Ester 
• 1738-87-0 Z-Leu-ONp 
• 61058-42-2 Z-Pro-Gly-OMe 
• 35010-96-9 Nα-benzyloxycarbonyl-L-prolyl-glycinamide 
• 3304-59-4 N-benzyloxycarbonyl-L-proline p-nitrophenyl ester 
• 41271-83-4 Z-(O₂N)Arg-Pro-Gly-NH₂ 

Downstream Products

• 33515-09-2 gonadotropin releasing hormone 
• 77659-12-2 Z-D-Ala-Leu-(O₂N)Arg-Pro-Gly-NH₂ 
• 77659-17-7 Z-Pro-Ser-Tyr-D-Ala-Leu-(O₂N)Arg-Pro-Gly-NH₂ 

Relevant academic research and scientific papers

Synthesis of Gonadoliberin, a Gonadotropin Releasing Hormone

A simple laboratory synthesis of gonadoliberin was elaborated basing on classical solution methods and using minimal protection of the side-chain functions.In the final step a hexapeptide segment was condensed with the corresponding tetrapeptide and the obtained product was purified by a single step silica gel chromatography.The total efficiency of the whole synthesis was 15percent.

SYNTHESIS OF 3(NH2); Pro3; D-Ala6>- and 2(NO2); Pro3; D-Ala6>LULIBERINS

In order to study the influence of substituents of the aromatic ring of D-phenylalanine on the inhibiting capacity of luliberian analogs, we have synthesized two new analogs: 2; Pro3; D-Ala6>- and