N-(Substituted-anilinoethyl)amides: Design, Synthesis, and Pharmacological Characterization of a New Class of Melatonin Receptor Ligands

S Rivara, A Lodola, M Mor, A Bedini… - Journal of medicinal …, 2007 - ACS Publications
A novel series of melatonin receptor ligands, characterized by a N-(substituted-anilinoethyl)
amido scaffold, along with preliminary structure–activity relationships (SARs), is presented …

2-[(2,3-Dihydro-1H-indol-1-yl)methyl]melatonin Analogues: A Novel Class of MT2-Selective Melatonin Receptor Antagonists

DP Zlotos, MI Attia, J Julius, S Sethi… - Journal of medicinal …, 2009 - ACS Publications
A novel series of 2-[(2, 3-dihydro-1 H-indol-1-yl) methyl] melatonin analogues has been
prepared to probe the steric and electronic properties of the binding pocket of the MT2 …

Synthesis, NMR conformational analysis and pharmacological evaluation of 7, 7a, 13, 14-tetrahydro-6 H-cyclobuta [b] pyrimido [1, 2-a: 3, 4-a′] diindole analogues as …

MI Attia, D Güclü, B Hertlein, J Julius… - Organic & …, 2007 - pubs.rsc.org
A structure for the self-condensation product of 2-(1H-indol-2-yl) ethyl tosylate2a, previously
proposed as 6, 7, 14, 15-tetrahydro-15aH-azocino [1, 2-a: 6, 5-b] diindole3a, was revised …

Synthesis and pharmacological evaluation of 1, 2, 3, 4-tetrahydropyrazino [1, 2-a] indole and 2-[(phenylmethylamino) methyl]-1H-indole analogues as novel …

C Markl, MI Attia, J Julius, S Sethi… - Bioorganic & medicinal …, 2009 - Elsevier
Two novel series of melatonin-derived compounds have been synthesized and
pharmacologically evaluated at the MT1 and MT2 subtypes of melatonin receptors …

Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligands

S Poissonnier-Durieux, M Ettaoussi, B Pérès… - Bioorganic & medicinal …, 2008 - Elsevier
A series of naphthalenic analogues of melatonin were prepared and evaluated as melatonin
receptor MT2 selective ligands. Activity and MT2 selectivity can be modulated with suitable …

Synthesis of 2-arylfuro [3, 2-b] pyridines: Effect of the C2-aryl group on melatoninergic activity

A Couhert, P Delagrange, DH Caignard… - European Journal of …, 2016 - Elsevier
We report herein an efficient synthesis of 2-substituted furo [3, 2-b] pyridines and their
biological evaluation as melatonin receptors ligands. The proposed eight-step sequence …

The Literature of Heterocyclic Chemistry, Part X, 2005–2007

LI Belen'kii, VN Gramenitskaya… - Advances in Heterocyclic …, 2011 - Elsevier
Publisher Summary This chapter is a sequel to nine already published surveys in “Advances
in Heterocyclic Chemistry”. It includes a list of monographs and reviews published during the …

Synthesis, Enantiomeric Resolution, and Structure–Activity Relationship Study of a Series of 10,11‐Dihydro‐5H‐Dibenzo[a,d]cycloheptene MT2 Receptor …

G Spadoni, A Bedini, G Diamantini… - ChemMedChem …, 2007 - Wiley Online Library
Abstract Racemic N‐(8‐methoxy‐10, 11‐dihydro‐5H‐dibenzo [a, d] cyclohepten‐10‐
ylmethyl) acetamide (compound 5) was previously identified as a novel selective MT2 …

2-[(1, 3-Dihydro-2 H-isoindol-2-yl) methyl] melatonin–a novel MT 2-selective melatonin receptor antagonist

D Heckman, MI Attia, MAM Behnam, AMY Mohsen… - …, 2011 - pubs.rsc.org
A synthesis and pharmacological evaluation of new melatonin receptor ligands obtained by
2-substitution of melatonin with (indol-1-yl) methyl,(isoindolin-2-yl) methyl, and …

Design and synthesis of 1-(2-alkanamidoethyl)-6-methoxy-7-azaindole derivatives as potent melatonin agonists

M Jeanty, F Suzenet, P Delagrange, O Nosjean… - Bioorganic & medicinal …, 2011 - Elsevier
A series of 7-azaindolic ligands bearing a methoxy group and a N-acetyl chain as
melatoninergic pharmacophores were synthesized and their binding affinities towards MT1 …