Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H19N5O4S |
Molecular Weight | 377.418 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=CC2=C(C=C1C3=CC=NN3C)C(=O)N(NS(C)(=O)=O)C(=O)N2
InChI
InChIKey=MCECSFFXUPEPDB-UHFFFAOYSA-N
InChI=1S/C16H19N5O4S/c1-9(2)10-8-13-12(7-11(10)14-5-6-17-20(14)3)15(22)21(16(23)18-13)19-26(4,24)25/h5-9,19H,1-4H3,(H,18,23)
Selurampanel (previously known as BGG 492), an orally available, AMPA-type glutamate receptor (AMPAR)/kainate receptor (GluK1; GluR5) antagonist was developed by Novartis. It is known that AMPAR antagonism is under development as a novel mechanism of action for antiepileptic drugs. Selurampanel was studied in phase II clinical trial for the migraine treatment. However, Proof-of-concept criterion was not met. In addition, the drug also participated in phase II clinical trials in therapy-refractory partial seizures for epilepsy surgery and in patients with chronic subjective tinnitus. Development of selurampanel for all these diseases was discontinued as of September 2017.
Approval Year
PubMed
Title | Date | PubMed |
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Randomized, multicenter trial to assess the efficacy, safety and tolerability of a single dose of a novel AMPA receptor antagonist BGG492 for the treatment of acute migraine attacks. | 2014 Feb |
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BGG492 (selurampanel), an AMPA/kainate receptor antagonist drug for epilepsy. | 2014 Jan |
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Design and Synthesis of Selurampanel, a Novel Orally Active and Competitive AMPA Receptor Antagonist. | 2017 Feb 3 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23963355
BGG492 (SELURAMPANEL) (250 mg), vs placebo and sumatriptan (100 mg), in 75 subjects with acute migraine attacks
Route of Administration:
Oral
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C264
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ACTIVE MOIETY