Foliglurax

Foliglurax
Clinical data
Other names	DT2331; PXT-002331; PXT-2331
Identifiers
	IUPAC name 4-[3-[4-nitroso-2-(5H-thieno[3,2-c]pyridin-6-ylidene)chromen-6-yl]propyl]morpholine;
PubChem CID	129320518;
ChemSpider	59718537;
Chemical and physical data
Formula	C23H23N3O3S
Molar mass	421.52 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C1COCCN1CCCC2=CC3=C(C=C2)OC(=C4C=C5C(=CN4)C=CS5)C=C3N=O;
	InChI InChI=1S/C23H23N3O3S/c27-25-19-13-22(20-14-23-17(15-24-20)5-11-30-23)29-21-4-3-16(12-18(19)21)2-1-6-26-7-9-28-10-8-26/h3-5,11-15,24H,1-2,6-10H2; Key:XHRLGFLGWZIPEE-UHFFFAOYSA-N;

Foliglurax (developmental code names PXT-002331, DT2331) is a positive allosteric modulator of the metabotropic glutamate receptor 4 (mGluR₄) which is under development by Prexton Therapeutics for the treatment of Parkinson's disease.[1][2] As of July 2017, it is in phase II clinical trials.[1]

The other tautomeric form of foliglurax.

References

"Foliglurax - Lundbeck". Adis Insight. Springer Nature Switzerland AG.
Jankovic J, Aguilar LG (August 2008). "Current approaches to the treatment of Parkinson's disease". Neuropsychiatric Disease and Treatment. 4 (4): 743–57. doi:10.1016/j.bmcl.2017.07.075. PMC 2536542. PMID 19043519.

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