174077-47-5

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 37993-32-1 1-amino-cyclohexanecarboxylic acid methyl ester hydrochloride 
• 4507-57-7 methyl 1-aminocyclohexanecarboxylate 
• 2756-85-6 1-aminocyclohexane carboxylic acid 

Downstream Products

• 1025955-34-3 Phe-Ac₆c-OMe 
• 174077-48-6 1-((S)-2-{(R)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-propionylamino}-3-phenyl-propionylamino)-cyclohexanecarboxylic acid methyl ester 
• 1026549-67-6 [(S)-1-{(R)-1-[(S)-1-(1-{(S)-1-[(S)-1-(Carbamoylmethyl-carbamoyl)-2-methyl-propylcarbamoyl]-2-methyl-propylcarbamoyl}-cyclohexylcarbamoyl)-2-phenyl-ethylcarbamoyl]-ethylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Tripeptide based super-organogelators: Structure and function

A novel series of tripeptide-based low molecular weight super-organogelators were synthesized and characterized. Four tripeptides with diverse steric crowding at the central amino acid residue were studied. From this series, only sterically less hindered

Design and synthesis of 1-aminocycloalkane-1-carboxylic acid-substituted deltorphin analogues: unique delta and mu opioid activity in modified peptides.

Deltorphin analogues were substituted by a series of achiral C alpha,alpha-dialkyl cyclic alpha-amino acids (1-aminocycloalkane-1-carboxylic acids, Ac chi c, where chi = a hexane, pentane, or propane cycloalkane ring) in position 2, 3, 4, or 2 and 3 in de