Structure via PubChem · Public domain (PubChem)
fasoracetam
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Fasoracetam () is an experimental drug of the racetam group which was never marketed. It is a putative nootropic that failed to show sufficient efficacy in clinical trials for vascular dementia. The drug was also subsequently repurposed for treatment of a variety of other conditions, such as attention deficit hyperactivity disorder (ADHD), but effectiveness for ADHD was disappointing and development of fasoracetam for most other conditions has been discontinued as well. In any case, it remains under development for treatment of DiGeorge syndrome. In addition to its clinical development, fasora
In the Vinony graph
Within Vinony's link graph, fasoracetam is referenced by 35 other articles, and connects out to bioavailability, International Standard Book Number and urine.
It sits within the topics 1-Piperidinyl compounds, Carboxamides and Drugs missing an ATC code.
Its subject is documented across 8 Wikipedia language editions.
Chemical data
- Formula
- C10H16N2O2
- Molecular weight
- 196.25 g/mol
- IUPAC name
- (5R)-5-(piperidine-1-carbonyl)pyrrolidin-2-one
- SMILES
- C1CCN(CC1)C(=O)[C@H]2CCC(=O)N2
- InChIKey
- GOWRRBABHQUJMX-MRVPVSSYSA-N
- XLogP
- 0
- Polar surface area
- 49.4 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
- Indications
- attention deficit hyperactivity disorder
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 196.121
Show 4 more facts
- canonical SMILES
- C1CCN(CC1)C(=O)C2CCC(=O)N2
- chemical formula
- C₁₀H₁₆N₂O₂
- isomeric SMILES
- C1CCN(CC1)C(=O)[C@H]2CCC(=O)N2
- subject has role
- nootropic
Sources (2)
via Wikidata · CC0
~4 min read
Encyclopedic overview
8 sectionsContents
- Pharmacology
- Chemistry
- History
- Society and culture
- Legality
- Australia
- Research
- References
Fasoracetam () is an experimental drug of the racetam group which was never marketed. It is a putative nootropic that failed to show sufficient efficacy in clinical trials for vascular dementia. The drug was also subsequently repurposed for treatment of a variety of other conditions, such as attention deficit hyperactivity disorder (ADHD), but effectiveness for ADHD was disappointing and development of fasoracetam for most other conditions has been discontinued as well. In any case, it remains under development for treatment of DiGeorge syndrome. In addition to its clinical development, fasoracetam is sold online and used non-medically as a nootropic.
==Pharmacology== Fasoracetam appears to modulate and stimulate all three groups of metabotropic glutamate receptors (mGluRs). It has been found to improve certain aspects of cognitive function in rodent studies. The drug is orally bioavailable and is excreted mostly unchanged in urine.
Excerpted from Wikipedia’s “fasoracetam” article, available under the CC BY-SA 4.0 licence.