Bioorganic & Medicinal Chemistry Letters 2007-06-01

1,3-disubstituted 4-aminopiperidines as useful tools in the optimization of the 2-aminobenzo[a]quinolizine dipeptidyl peptidase IV inhibitors.

Thomas Lübbers, Markus Böhringer, Luca Gobbi, Michael Hennig, Daniel Hunziker, Bernd Kuhn, Bernd Löffler, Patrizio Mattei, Robert Narquizian, Jens-Uwe Peters, Yves Ruff, Hans Peter Wessel, Pierre Wyss

Index: Bioorg. Med. Chem. Lett. 17(11) , 2966-70, (2007)

Full Text: HTML

Abstract

In a search for novel DPP-IV inhibitors, 2-aminobenzo[a]quinolizines were identified as submicromolar HTS hits. Due to the difficult synthetic access to this compound class, 1,3-disubstituted 4-aminopiperidines were used as model compounds for optimization. The developed synthetic methodology and the SAR could be transferred to the 2-aminobenzo[a]quinolizine series, leading to highly active DPP-IV inhibitors.


Related Compounds

Related Articles:

Topoisomerase II from Human Malaria Parasites: EXPRESSION, PURIFICATION, AND SELECTIVE INHIBITION.

2015-08-14

[J. Biol. Chem. 290 , 20313-24, (2015)]

Inhibition of metabolism--mediated cytotoxicity by 1,1-disubstituted hydrazines in mouse mastocytoma cells (line P815).

1981-01-01

[Adv. Exp. Med. Biol. 136 Pt B , 1067-75, (1981)]

Aerial oxidation of hydrazines to nitrosamines.

1991-01-01

[Environ. Mol. Mutagen. 17(1) , 59-62, (1991)]

More Articles...