International Union of Basic and Clinical Pharmacology. LXXV. Nomenclature, classification, and pharmacology of G protein-coupled melatonin receptors

ML Dubocovich, P Delagrange… - Pharmacological …, 2010 - pharmrev.aspetjournals.org
The hormone melatonin (5-methoxy-N-acetyltryptamine) is synthesized primarily in the
pineal gland and retina, and in several peripheral tissues and organs. In the circulation, the …

Synthetic approaches to 3-(2-nitroalkyl) indoles and their use to access tryptamines and related bioactive compounds

S Lancianesi, A Palmieri, M Petrini - Chemical Reviews, 2014 - ACS Publications
The assembly of architecturally complex alkaloids embedding the indole nucleus is of
paramount importance for the target oriented synthesis of biologically active molecules. 1 A …

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

DP Zlotos, R Jockers, E Cecon, S Rivara… - Journal of medicinal …, 2014 - ACS Publications
Numerous physiological functions of the pineal gland hormone melatonin are mediated via
activation of two G-protein-coupled receptors, MT1 and MT2. The melatonergic drugs on the …

CoIII–Carbene Radical Approach to Substituted 1H-Indenes

BG Das, A Chirila, M Tromp, JNH Reek… - Journal of the …, 2016 - ACS Publications
A new strategy for the catalytic synthesis of substituted 1 H-indenes via metalloradical
activation of o-cinnamyl N-tosyl hydrazones is presented, taking advantage of the intrinsic …

Mapping the melatonin receptor. 6. Melatonin agonists and antagonists derived from 6 H-isoindolo [2, 1-a] indoles, 5, 6-dihydroindolo [2, 1-a] isoquinolines, and 6, 7 …

R Faust, PJ Garratt, R Jones, LK Yeh… - Journal of medicinal …, 2000 - ACS Publications
6 H-Isoindolo [2, 1-a] indoles (5, 7, 10, 13), 5, 6-dihydroindolo [2, 1-a] isoquinolines (20, 21),
and 6, 7-dihydro-5 H-benzo [c] azepino [2, 1-a] indoles (23, 25, 27, 30) have been prepared …

Dehydration triggered asymmetric hydrogenation of 3-(α-hydroxyalkyl) indoles

DS Wang, J Tang, YG Zhou, MW Chen, CB Yu… - Chemical …, 2011 - pubs.rsc.org
Highly enantioselective hydrogenation of 3-(α-hydroxyalkyl) indoles promoted by a Brønsted
acid for dehydration to form a vinylogous iminium intermediate in situ was developed with …

Melatonin receptor ligands: a pharmaco‐chemical perspective

JA Boutin, PA Witt‐Enderby, C Sotriffer… - Journal of pineal …, 2020 - Wiley Online Library
Melatonin MT1 and MT2 receptor ligands have been vigorously explored for the last 4
decades. Inspection of approximately 80 publications in the field revealed that most …

Indole-based melatonin analogues: Synthetic approaches and biological activity

SY Wang, XC Shi, P Laborda - European Journal of Medicinal Chemistry, 2020 - Elsevier
Melatonin is a natural hormone primarily released by the pineal gland that regulates the
sleep-wake cycles. The diverse biological applications of melatonin, together with the need …

Cardioprotective melatonin: translating from proof-of-concept studies to therapeutic use

OC Baltatu, S Senar, LA Campos… - International Journal of …, 2019 - mdpi.com
In this review we summarized the actual clinical data for a cardioprotective therapeutic role
of melatonin, listed melatonin and its agonists in different stages of development, and …

Melatonin analogues potently inhibit MAO-B and protect PC12 cells against oxidative stress

A Elkamhawy, J Woo, NA Gouda, J Kim, H Nada… - Antioxidants, 2021 - mdpi.com
Monoamine oxidase B (MAO-B) metabolizes dopamine and plays an important role in
oxidative stress by altering the redox state of neuronal and glial cells. MAO-B inhibitors are a …