Development of a novel NURR1/NOT agonist from hit to lead and candidate for the potential treatment of Parkinson's disease
- Bioorg Med Chem Lett. 2019 Apr 1;29(7):929-932. doi: 10.1016/j.bmcl.2019.01.024.
- 1. Rare and Neurologic Disease Research, Sanofi, 1 av Pierre Brossolette, Chilly Mazarin F-91935, France. Electronic address: [email protected].
- 2. Medicinal Chemistry, Sanofi, 1 av Pierre Brossolette, Chilly Mazarin F-91385, France.
- 3. DMPK, Sanofi, 13 quai Jules Guesde, Vitry-sur-Seine F-94403, France.
- 4. Rare and Neurologic Disease Research, Sanofi, 1 av Pierre Brossolette, Chilly Mazarin F-91935, France.
- 5. Preclinical Safety, Sanofi, 3, digue d' Alfortville, Alfortville F-94140, France.
- 6. Translational Science, Sanofi, 1 av Pierre Brossolette, Chilly Mazarin F-91385, France.
- 7. CNS Department, Sanofi, 195 route d'Espagne, F-31036 Toulouse, France.
- 8. CNS Department, 13, quai Jules Guesde, F-94403 Vitry-sur-Seine Cedex, France.
In the course of a programme aimed at identifying Nurr1/NOT agonists for potential treatment of Parkinson's disease, a few hits from high throughput screening were identified and characterized. A combined optimization pointed to a very narrow and stringent structure activity relationship. A comprehensive program of optimization led to a potent and safe candidate drug displaying neuroprotective and anti-inflammatory activity in several in vitro and in vivo models.