Novel difluoroacetamide analogues of agomelatine and melatonin: probing the melatonin receptors for MT1selectivity

Author:

Zlotos Darius P.1234,Riad Noura M.1234,Osman Mai B.1234,Dodda Bala R.56789,Witt-Enderby Paula A.56789

Affiliation:

1. Department of Pharmaceutical Chemistry

2. The German University in Cairo

3. New Cairo City

4. Egypt

5. Division of Pharmaceutical Sciences

6. School of Pharmacy

7. Duquesne University

8. 421 Mellon Hall

9. Pittsburgh

Abstract

The difluoroacetamide analogue of the standard MT1-selective ligand, the dimeric (CH2)3-linked agomelatine, shows higher affinity and selectivity toward MT1receptors than the parent compound.

Funder

German Academic Exchange Service

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Reference25 articles.

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3. MT1 and MT2 Melatonin Receptors: Ligands, Models, Oligomers, and Therapeutic Potential

4. Targeted Disruption of the Mouse Mel 1b Melatonin Receptor

5. Melatonin modulates visual function and cell viability in the mouse retina via the MT1 melatonin receptor

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