368448-99-1

Upstream product

• 368448-91-3 methyl (3R,4E,αS)-3-(N-benzyl-N-α-methylbenzylamino)-5-phenylpent-4-enoate 
• 368448-95-7 methyl (3R,4E)-3-(N-tert-butoxycarbonylamino)-5-phenylpent-4-enoate 
• 170726-18-8 methyl (3S)-3-amino-5-phenylpentanoate 
• 158807-52-4 methyl (3S)-3-(N-tert-butoxycarbonylamino)-5-phenylpentanoate 
• 38447-05-1 (2E,4E)-methyl 5-phenylpenta-2,4-dienoate 
• 52161-76-9 (E,2S)-2-amino-5-phenyl-pent-4-enoic acid 
• 368448-97-9 (3R,4E)-3-(N-tert-butoxycarbonylamino)-5-phenylpent-4-enoic acid 

Downstream Products

• 368449-01-8 (3R,4E)-3-[N-(fluoren-9-ylmethoxycarbonyl)amino]-5-phenylpent-4-enoic acid 

Relevant academic research and scientific papers

β-styryl- and β-aryl-β-alanine products of phenylalanine aminomutase catalysis

The substrate specificity of a Taxus-derived phenylalanine aminomutase (PAM) was investigated, and the enzyme was found to catalyze the conversion of variously substituted vinyl- and aryl-S-∞-alanines to corresponding β-amino acids. This study shows the b

Serine-threonine protein phosphatase inhibitors derived from nodularin: Role of the 2-methyl and 3-diene groups in the Adda residue and the effect of macrocyclic conformational restraint

In order to probe the effect upon macrocycle conformation and PP1cat enzyme inhibition of structural changes to nodularin, specific replacements for the Adda residue were introduced. Two new analogues, cyclo[-(3S,E)-3-phenylethenyl-3-aminopropa