75895-00-0

Upstream product

• 41444-88-6 L-glutamine tert-butyl ester 
• 1148-11-4 N-Benzyloxycarbonyl-L-proline 
• 3304-59-4 N-benzyloxycarbonyl-L-proline p-nitrophenyl ester 

Downstream Products

• 406712-27-4 Z-Tyr-Pro-Gln-Ot-Bu 
• 406712-37-6 Z-Val-Tyr-Pro-Gln-Ot-Bu 
• 406712-34-3 (S)-2-({(S)-1-[(S)-2-((S)-2-Benzyloxycarbonylamino-3-tert-butoxy-propionylamino)-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid tert-butyl ester 
• 406712-28-5 (S)-2-({(S)-1-[(S)-2-[(R)-3-(Acetylamino-methylsulfanyl)-2-tert-butoxycarbonylamino-propionylamino]-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid tert-butyl ester 
• 406712-38-7 Z-Val-Val-Tyr-Pro-Gln-Ot-Bu 
• 406712-35-4 (S)-2-({(S)-1-[(S)-2-[(S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-3-tert-butoxy-propionylamino]-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid tert-butyl ester 
• 406712-39-8 Boc-Leu-Val-Val-Tyr-Pro-Gln-Ot-Bu 
• 406712-36-5 (S)-2-({(S)-1-[(S)-2-{(S)-3-tert-Butoxy-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid tert-butyl ester 
• 75903-32-1 Z-Thr(Bu^t)-Pro-Ile-Leu-Pro-Gln-OBu^t 
• 75895-15-7 Z-Pro-Ile-Leu-Pro-Gln-OBu^t 
• 75895-13-5 Z-Ile-Leu-Pro-Gln-OBu^t 
• 75895-01-1 Z-Leu-Pro-Gln-OBu^t 

Relevant academic research and scientific papers

Effect of the SH Group of Myelopeptide MP-3 on Its Macrophage Stimulating Activity

Peptide Leu-Val-Cys-Tyr-Pro-Gln, identical to the bone marrow peptide MP-3, and its Val3 and Ser3 analogs, lacking SH group, were synthesized by conventional methods of peptide chemistry in solution and, along with the MP-3 S-S-dimer

HUMAN CHORIONIC GONADOTROPIN. IV. SYNTHESIS OF A HEXADECAPEPTIDE CORRESPONDING TO THE C-TERMINAL SEQUENCE 130-145 OF THE β-SUBUNIT OF HUMAN CHORIONIC GONADOTROPIN (hCG)

The hexadecapeptide corresponding to sequence 130-145 of the β-subunit of human chorionic gonadotropin (hCG) according to the amino acid sequence proposed by Morgan et. al. was synthesized by successive azide condensation of 4 peptide fragments, followed