Issue 3, 2003
From the journal:

Chemical Communications

Design and synthesis of potent N1-substituted indolemelatonin receptor agonists†

Andrew Tsotinis,*a   Andreas Eleutheriades,a   Katherine Houghb  and  David Sugdenb  

* Corresponding authors

a Department of Pharmaceutical Chemistry, School of Pharmacy, University of Athens, Panepistimiopolis-Zografou, 157 71, Athens, Greece
E-mail: tsotinis@pharm.uoa.gr
Fax: +30 210 7274747
Tel: +30 210 7274812

b Centre for Reproduction, Endocrinology & Diabetes, Physiology Division, GKT School of Biomedical Sciences, New Hunts House, Kings College London, London Bridge, London, UK
E-mail: david.sugden@kcl.ac.uk
Fax: +44 020 7848 6280
Tel: +44 020 7848 6274

Abstract

The design and expeditious synthesis of two new indole analogs with up to 5-fold potency of that of melatonin is described.

Graphical abstract: Design and synthesis of potent N1-substituted indole melatonin receptor agonists

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Article information

DOI
https://doi.org/10.1039/B210731G
Article type
Communication
Submitted
31 Oct 2002
Accepted
03 Jan 2003
First published
14 Jan 2003

Chem. Commun., 2003, 382-383

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Design and synthesis of potent N1-substituted indole melatonin receptor agonists

A. Tsotinis, A. Eleutheriades, K. Hough and D. Sugden, Chem. Commun., 2003, 382 DOI: 10.1039/B210731G

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