Synthesis of unusual isoxazoline containing β and γ-dipeptides as potential glutamate receptor ligands

Lucia Tamborini; Federica Mastronardi; Federica Dall'Oglio; Carlo De Micheli; Birgitte Nielsen; Leonardo Lo Presti; Paola Conti; Andrea Pinto

doi:10.1039/c5md00159e

Synthesis of unusual isoxazoline containing β and γ-dipeptides as potential glutamate receptor ligands

Lucia Tamborini, Federica Mastronardi, Federica Dall'Oglio, Carlo De Micheli, Birgitte Nielsen, Leonardo Lo Presti, Paola Conti, Andrea Pinto

4 Citations (Scopus)

Abstract

New unconventional beta and gamma dipeptides, representing conformationally constrained higher homologues of glutamic acid, have been prepared and tested as new pharmacological tools to investigate the iGluR binding domain, in an attempt to identify potential selective antagonists.

Original language	English
Journal	MedChemComm
Volume	6
Issue number	7
Pages (from-to)	1260-1266
Number of pages	7
ISSN	2040-2503
DOIs	https://doi.org/10.1039/c5md00159e
Publication status	Published - 1 Jul 2015

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@article{43dacdaf73214b71bf68381436ece364,

title = "Synthesis of unusual isoxazoline containing β and γ-dipeptides as potential glutamate receptor ligands",

abstract = "New unconventional beta and gamma dipeptides, representing conformationally constrained higher homologues of glutamic acid, have been prepared and tested as new pharmacological tools to investigate the iGluR binding domain, in an attempt to identify potential selective antagonists.",

author = "Lucia Tamborini and Federica Mastronardi and Federica Dall'Oglio and {De Micheli}, Carlo and Birgitte Nielsen and {Lo Presti}, Leonardo and Paola Conti and Andrea Pinto",

year = "2015",

month = jul,

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doi = "10.1039/c5md00159e",

language = "English",

volume = "6",

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journal = "MedChemComm",

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T1 - Synthesis of unusual isoxazoline containing β and γ-dipeptides as potential glutamate receptor ligands

AU - Tamborini, Lucia

AU - Mastronardi, Federica

AU - Dall'Oglio, Federica

AU - De Micheli, Carlo

AU - Nielsen, Birgitte

AU - Lo Presti, Leonardo

AU - Conti, Paola

AU - Pinto, Andrea

PY - 2015/7/1

Y1 - 2015/7/1

N2 - New unconventional beta and gamma dipeptides, representing conformationally constrained higher homologues of glutamic acid, have been prepared and tested as new pharmacological tools to investigate the iGluR binding domain, in an attempt to identify potential selective antagonists.

AB - New unconventional beta and gamma dipeptides, representing conformationally constrained higher homologues of glutamic acid, have been prepared and tested as new pharmacological tools to investigate the iGluR binding domain, in an attempt to identify potential selective antagonists.

U2 - 10.1039/c5md00159e

DO - 10.1039/c5md00159e

M3 - Journal article

SN - 2040-2503

VL - 6

SP - 1260

EP - 1266

JO - MedChemComm

JF - MedChemComm

IS - 7

ER -

Synthesis of unusual isoxazoline containing β and γ-dipeptides as potential glutamate receptor ligands

Abstract

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