58111-84-5

Upstream product

• 13673-57-9 N-(benzyloxycarbonyl)-L-serine pentachlorophenyl ester 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 1080-06-4 L-Tyr-OMe 
• 24118-03-4 Z-L-Ser-L-Tyr-OMe 
• 55610-27-0 Z-L-Ser-L-Tyr-N₂H₃ 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 

Downstream Products

• 85476-30-8 H-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg-L-Pro-NHEt 
• 85476-31-9 Z-D-Phe-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg-L-Pro-NHEt 
• 85476-29-5 Z-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-L-Arg(NO₂)-L-Pro-NHEt 
• 77659-16-6 Z-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-N₂H₃ 
• 77659-15-5 Z-L-Pro-L-Ser-L-Tyr-D-Ala-L-Leu-OMe 
• 132478-01-4 (S)-1-[(S)-2-((S)-2-{(R)-2-[(S)-2-((S)-2-Amino-3-hydroxy-propionylamino)-3-(4-hydroxy-phenyl)-propionylamino]-3-phenyl-propionylamino}-4-methyl-pentanoylamino)-5-guanidino-pentanoyl]-pyrrolidine-2-carboxylic acid carbamoylmethyl-amide 
• 64152-92-7 Z-L-Ser-L-Tyr-D-Ala-L-Leu-OMe 
• 171976-99-1 (R)-2-[(S)-2-((S)-2-Benzyloxycarbonylamino-3-hydroxy-propionylamino)-3-(4-hydroxy-phenyl)-propionylamino]-succinic acid 4-benzyl ester 
• 171976-97-9 Z-Ser-Tyr-D-Asp(OBzl)-Leu-Arg(NO₂)-Pro-NHEt 
• 171976-98-0 C₄₅H₇₁N₁₁O₁₃ 
• 171976-95-7 (R)-N-{(S)-1-[(S)-1-((S)-2-Ethylcarbamoyl-pyrrolidine-1-carbonyl)-4-guanidino-butylcarbamoyl]-3-methyl-butyl}-3-((S)-3-(4-hydroxy-phenyl)-2-{(S)-3-hydroxy-2-[((S)-pyrrolidine-2-carbonyl)-amino]-propionylamino}-propionylamino)-succinamic acid 
• 171976-93-5 (R)-3-[(S)-2-((S)-2-Amino-3-hydroxy-propionylamino)-3-(4-hydroxy-phenyl)-propionylamino]-N-{(S)-1-[(S)-1-((S)-2-ethylcarbamoyl-pyrrolidine-1-carbonyl)-4-guanidino-butylcarbamoyl]-3-methyl-butyl}-succinamic acid 

Relevant academic research and scientific papers

SYNTHESIS AND INVESTIGATION OF THE ANTITUMORAL ACTIVITY OF SHORTENED ANALOGS OF LULIBERIN

With the aim of obtaining antitumoral drugs possessing a binary action mechanism, we have synthesized a series of shortened analogs of luliberin, including some containing a 1-carboxymethyl-5-fluorouracil residue.Their antitumoral and hormonal activities

SYNTHESIS OF BIOLOGICALLY ACTIVE ANALOGS OF LULIBERIN WITH SHORTENED AMINO ACID SEQUENCES

Two new analogs of the releasing factor of the luteinizing hormone with shortened amino acid sequences have been synthesized by the methods of classical peptide chemistry.The influence of the preparations on the action of chorionic gonadotropin and on the