Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H15N3O2S |
Molecular Weight | 253.321 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)OCCN1C2=C(NC=C2)C(=O)NC1=S
InChI
InChIKey=FVJCUZCRPIMVLB-UHFFFAOYSA-N
InChI=1S/C11H15N3O2S/c1-7(2)16-6-5-14-8-3-4-12-9(8)10(15)13-11(14)17/h3-4,7,12H,5-6H2,1-2H3,(H,13,15,17)
Verdiperstat (formerly known as AZD 3241) was developed as a selective inhibitor of myeloperoxidase, an enzyme that acts as a key driver of pathological oxidative stress and inflammation in the brain. Verdiperstat was studied in patients with a number of neurodegenerative disorders, including multiple system atrophy and Parkinson's disease. Verdiperstat participated in phase II clinical trials for both diseases. As a result, studies for Parkinson disease were discontinued. In the case of multiple system atrophy, the drug has received the orphan drug status.
CNS Activity
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT02388295
Drug: AZD3241 administered for 12 weeks orally as a tablet.
Route of Administration:
Oral
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EU-Orphan Drug |
EU/3/14/1404
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NCI_THESAURUS |
C1509
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FDA ORPHAN DRUG |
671418
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NCI_THESAURUS |
C471
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890655-80-8
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DB12440
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C152861
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100000175356
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10251
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TT3345YXVR
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GH-157
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11528958
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ACTIVE MOIETY