Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H18N2O2 |
Molecular Weight | 246.3049 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N1CCN(CC1)C(=O)C2=CC=CC=C2
InChI
InChIKey=DGOWDUFJCINDGI-UHFFFAOYSA-N
InChI=1S/C14H18N2O2/c1-2-13(17)15-8-10-16(11-9-15)14(18)12-6-4-3-5-7-12/h3-7H,2,8-11H2,1H3
Molecular Formula | C14H18N2O2 |
Molecular Weight | 246.3049 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/16834757Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/14600801 | https://www.ncbi.nlm.nih.gov/pubmed/18954993 | https://www.ncbi.nlm.nih.gov/pubmed/11087574 | https://www.ncbi.nlm.nih.gov/pubmed/23295391
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16834757
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/14600801 | https://www.ncbi.nlm.nih.gov/pubmed/18954993 | https://www.ncbi.nlm.nih.gov/pubmed/11087574 | https://www.ncbi.nlm.nih.gov/pubmed/23295391
Sunifiram (DM235) is a piperazine derived research chemical which has anti-amnesiac effects in animal studies. Though Sunifiram is a piracetam derivative, it has a different chemical structure from the racetams and is chemically classed as a piperazine alkaloid. It is known to work in two ways, both as an ampakine that stimulates the activity of glutamine receptors and as a cholinergic that increases the production and release of acetylcholine. Like many nootropics, Sunifiram’s precise mechanisms of action are not entirely understood. However, it is believed that its primary action is that of an ampakine, which means that after crossing the blood-brain barrier it binds to AMPA-type glutamate receptors in the brain. This stimulates the production of glutamate, a vital neurotransmitter that plays the pivotal role in neural activation. Sunifiram is also thought to act as a cholinergic, increasing the production and release of the neurotransmitter acetylcholine. Though the exact process by which this occurs has not been identified, an Italian animal study showed that tests using piperazine compounds such as Sunifiram had a cholinergic effect similar to that of piracetam. No serious side effects of Sunifiram have been documented, but it’s important to remember that no human studies or clinical trials have been conducted.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2096670 Sources: https://www.ncbi.nlm.nih.gov/pubmed/14600801 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
mice: 0.01–0.1 mg/kg i.p
mice: 0.1-1.0 mg/kg p.o.
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16834757
Rat hippocampal slices were used for activity evaluation. Slices were superfused with Mg2+-free medium from t = 0 min of superfusion. NBQX was added
concomitantly with kynurenate and sunifiram, at t = 30 min till the end of superfusion.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:00:30 GMT 2023
by
admin
on
Sat Dec 16 08:00:30 GMT 2023
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Record UNII |
66924E735K
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Record Status |
Validated (UNII)
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Record Version |
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SUNIFIRAM
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4223812
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DTXSID10400996
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66924E735K
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314728-85-3
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admin on Sat Dec 16 08:00:30 GMT 2023 , Edited by admin on Sat Dec 16 08:00:30 GMT 2023
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ACTIVE MOIETY |