Pariceract
Pharmaceutical compound
From Wikipedia, the free encyclopedia
Pariceract (INN; developmental code name BIA 28-6156 or LTI-291) is a β-glucocerebrosidase (GCase) activator or positive allosteric modulator which is under development for the treatment of Parkinson's disease.[1][2][3][4][5] It is taken orally.[1] GCase is a lysosomal enzyme encoded by the gene GBA1.[4][5] Loss-of-function mutations in this gene are thought to promote α-synuclein accumulation and are among the leading genetic risk factors for Parkinson's disease.[4][5][6] As such, activation of GCase might provide a disease-modifying therapy for treatment of Parkinson's disease.[4][5] Pariceract was first described in the scientific literature by 2017.[6] It was originated by Lysosomal Therapeutics and is under development by Lysosomal Therapeutics and Bial.[1][2][3] As of October 2025, it is in phase 2 clinical trials.[1][2][3]
| Clinical data | |
|---|---|
| Other names | BIA 28-6156; LTI-291; LIT291; LTI-00291 |
| Routes of administration | Oral[1] |
| Drug class | β-Glucocerebrosidase (GCase) activator or positive allosteric modulator |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| Chemical and physical data | |
| Formula | C20H30N4O2 |
| Molar mass | 358.486 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
See also
- List of investigational Parkinson's disease drugs
- GT-02287 (possibly rexaceract)
- Ambroxol