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Items: 3

1.

[b]-Annulated Halogen-Substituted Indoles as Potential DYRK1A Inhibitors.

Lechner C, Flaßhoff M, Falke H, Preu L, Loaëc N, Meijer L, Knapp S, Chaikuad A, Kunick C.

Molecules. 2019 Nov 13;24(22). pii: E4090. doi: 10.3390/molecules24224090.

2.

Indole-3-Carbonitriles as DYRK1A Inhibitors by Fragment-Based Drug Design.

Meine R, Becker W, Falke H, Preu L, Loaëc N, Meijer L, Kunick C.

Molecules. 2018 Jan 24;23(2). pii: E64. doi: 10.3390/molecules23020064.

3.

10-iodo-11H-indolo[3,2-c]quinoline-6-carboxylic acids are selective inhibitors of DYRK1A.

Falke H, Chaikuad A, Becker A, Loaëc N, Lozach O, Abu Jhaisha S, Becker W, Jones PG, Preu L, Baumann K, Knapp S, Meijer L, Kunick C.

J Med Chem. 2015 Apr 9;58(7):3131-43. doi: 10.1021/jm501994d. Epub 2015 Mar 23.

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