141982-67-4

Upstream product

• 13139-14-5 Boc-Trp-OH 
• 142003-28-9 H-(N-Me)Asp(OBn)-Phe-NH₂ hydrochloride 
• 199541-43-0 (S)-3-[((S)-2-tert-Butoxycarbonylamino-hexanoyl)-methyl-amino]-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid benzyl ester 
• 199541-42-9 (S)-3-(tert-Butoxycarbonyl-methyl-amino)-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid benzyl ester 
• 141408-45-9 (S)-4-(benzyloxy)-2-((tert-butoxycarbonyl)(methyl)amino)-4-oxobutanoic acid 
• 65864-22-4 (S)-2-amino-3-phenylpropionamide hydrochloride 
• 127476-51-1 C₂₁H₂₈N₂O₆ 

Downstream Products

• 199541-49-6 (S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester 
• 152548-36-2 Hpa-Nle-Gly-Trp-Nle-MeAsp-Phe-NH₂ 
• 152548-39-5 AR-R 15849 
• 141982-68-5 H-Trp-Nle-(N-Me)Asp-Phe-NH₂ 

Relevant academic research and scientific papers

Synthesis and biological evaluation of potent, selective, hexapeptide CCK-A agonist anorectic agents

Cholecystokinin (CCK) is a 33-amino acid peptide with multiple functions in both the central nervous system (via CCK-B receptors) and the periphery (via CCK-A receptors). CCK mediation of satiety via the A-receptor subtype suggest a role for CCK in the ma

Synthesis and Biological Activity of CCK Heptapeptide Analogues. Effects of Conformational Constraints and Standard Modifications on Receptor Subtype Selectivity, Functional Activity in Vitro, and Appetite Suppression in Vivo

A series of modifications of the CCK7 analogue (des-NH2)Tyr(SO3-)-Nle-Gly-Trp-Nle-Asp-Phe-NH2 was prepared and tested for binding to guinea pig CCK-A and CCK-B receptors and in CCK-A-mediated functional assays.Selected analogues also were teste