80887-26-9

Upstream product

• 80887-21-4 2-acetylamino-2-(4-phenyl-butyl)malonic acid diethyl ester 
• 13633-25-5 1-Bromo-4-phenylbutane 
• 150823-78-2 (S)-2-acetamido-6-phenylhexanoic acid 

Downstream Products

• 150722-68-2 (S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid 
• 150722-70-6 (S)-2<(tert-butyloxycarbonyl)amino>-7-phenylheptanoic acid 
• 150722-83-1 (S)-benzyl 2<(tert-butyloxycarbonyl)amino>-7-phenylheptanoate 
• 150722-87-5 Boc-Nle-(S)-β-homo-Aph-OBzl 

Relevant academic research and scientific papers

Synthesis method of multi-configuration long-chain phenyl amino acid compound

The invention relates to a method for synthesizing a multi-configuration long-chain phenyl amino acid compound. The method comprises the following steps: reacting a compound shown in a formula I witha compound shown in a formula II or an isomer thereof in

Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid

Boc-Tyr(SO3H)-Nle-Gly-Trp-Nle-Asp-2-phenylethyl ester (JMV180), an analog of the C-terminal octapeptide of cholecystokinin (CCK-8), shows interesting biological activities behaving as an agonist at the high-affinity CCK binding sites and as an