Potent and Orally Bioavailable Inverse Agonists of RORγt Resulting from Structure-Based Design.

Publication

Citation
Narjes F, Xue Y, von Berg S, Malmberg J, Llinas A, Olsson RI, Jirholt J, Grindebacke H, Leffler A, Hossain N, Lepistö M, Thunberg L, Leek H, Aagaard A, McPheat J, Hansson EL, Bäck E, Tångefjord S, Chen R, Xiong Y, Hongbin G, Hansson TG.: Potent and Orally Bioavailable Inverse Agonists of RORγt Resulting from Structure-Based Design. J Med Chem, Volume 61 (17), 2018
Authors
Aagaard A, Bäck E, Chen R, Grindebacke H, Hansson EL, Hansson TG., Hongbin G, Hossain N, Jirholt J, Leek H, Leffler A, Lepistö M, Llinas A, Malmberg J, McPheat J, Narjes F, Olsson RI, Tångefjord S, Thunberg L, von Berg S, Xiong Y, Xue Y
Journal
J Med Chem
Year
2018
PubMed
30095900
Machine-readable
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Palacky University Olomouc

Palacky University Olomouc

Faculty of Science

Department of Physical Chemistry

tř. 17. listopadu 1192/12

771 46 Olomouc

Czech Republic

How to cite?

Juračka J., Šrejber M., Melíková M., Bazgier V., Berka K.: MolMeDB: Molecules on Membranes Database. Database, Volume 2019, 2019, baz078, https://doi.org/10.1093/database/baz078

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