Bioisosteric Replacement of Arylamide-Linked Spine Residues with N-Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type I 1/2 p38 alpha MAP Kinase Inhibitors

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Bioisosteric Replacement of Arylamide-Linked Spine Residues with N-Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type I 1/2 p38 alpha MAP Kinase Inhibitors

Author: Pedreira, Julia G. B.; Nahidino, Philipp; Kudolo, Mark; Pantsar, Tatu; Berger, Benedict-Tilman; Forster, Michael; Knapp, Stefan; Laufer, Stefan; Barreiro, Eliezer J.
Tübinger Autor(en):
Nahidino, Philipp
Kudolo, Mark
Pantsar, Tatu
Forster, Michael
Laufer, Stefan
Published in: Journal of Medicinal Chemistry (2020), Bd. 63, H. 13, S. 7347-7354
Verlagsangabe: Amer Chemical Soc
Language: English
Full text: http://dx.doi.org/10.1021/acs.jmedchem.0c00508
ISSN: 1520-4804
DDC Classifikation: 540 - Chemistry and allied sciences
Dokumentart: Article
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