Design, synthesis, and pharmacological characterization of novel endomorphin-1 analogues as extremely potent μ-opioid agonists

X Liu, Y Wang, Y Xing, J Yu, H Ji, M Kai… - Journal of Medicinal …, 2013 - ACS Publications
Recently we reported the synthesis and structure–activity study of endomorphin-1 (EM-1)
analogues containing novel, unnatural α-methylene-β-aminopropanoic acids (Map). In the …

Synthesis, pharmacological evaluation and conformational investigation of endomorphin-2 hybrid analogues

G Lesma, S Salvadori, F Airaghi, E Bojnik, A Borsodi… - Molecular …, 2013 - Springer
This study reports on new pharmacologically active endomorphin-2 analogues,
incorporating β 2-hPhe, β 3-hPhe and β 3-hTic unnatural amino acids in the place of the Phe …

An Efficient Synthesis and In Vitro Antibacterial Activity of Novel Spiro‐aminopyrimidones

S Balalaie, H Moghimi, M Bararjanian… - Journal of …, 2013 - Wiley Online Library
A highly efficient one‐pot synthesis of some new spiro‐2‐aminopyrimidinones via a three‐
component reaction of cyclic ketones, methylcyanoacetate or malononitrile, and …

An Efficient Synthesis and In Vitro.

S Balalaie, H Moghimi, M Bararjanian… - Journal of …, 2013 - search.ebscohost.com
A highly efficient of some new spiro-2-aminopyrimidinones via a three-component reaction
of cyclic ketones, methylcyanoacetate or malononitrile, and guanidinium carbonate has …

SYNTHESIS, STRUCTURAL INVESTIGATION AND BIOLOGICAL EVALUATION OF CONFORMATIONALLY CONSTRAINED PEPTIDOMIMETICS

F Airaghi - 2013 - air.unimi.it
This Ph. D. thesis is located in the medicinal chemistry research field. Peptides are among
the most studied entities as potential drug candidates, due to their natural abundance and …