Structure via PubChem · Public domain (PubChem)
unifiram
Sign in to saveUnifiram (developmental code name DM-232) is an experimental drug. that has antiamnesic and other effects in animal studies with far greater potency than piracetam. A number of related compounds are known, such as sunifiram (DM-235) and sapunifiram (MN-19). Unifiram has two enantiomers, with the dextro form being the more active isomer. It has been shown to reduce the duration of hypnosis induced by pentobarbital, without impairing motor coordination. , no formal human studies with unifiram have been conducted. Unifiram is not patented and, despite the lack of human and long-term toxicity stud
In the Vinony graph
Vinony's link graph records 517 inbound references to unifiram, and connects out to digital object identifier, chemical formula and amnesia.
It is catalogued under topics including 4-Fluorophenyl compounds, Chemical pages without DrugBank identifier and Designer drugs.
Vinony links it to 4 Wikipedia language editions.
Chemical data
- Formula
- C13H15FN2O3S
- Molecular weight
- 298.34 g/mol
- IUPAC name
- 2-(4-fluorophenyl)sulfonyl-1,3,4,7,8,8a-hexahydropyrrolo[1,2-a]pyrazin-6-one
- SMILES
- C1CC(=O)N2C1CN(CC2)S(=O)(=O)C3=CC=C(C=C3)F
- InChIKey
- SNRTZFZAFBIBJP-UHFFFAOYSA-N
- XLogP
- 0.6
- Polar surface area
- 66.1 Ų
- H-bond donors
- 0
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 298.079
Show 4 more facts
- Commons category
- Unifiram
- chemical formula
- C₁₃H₁₅FN₂O₃S
- subject has role
- nootropic
- canonical SMILES
- C1CC(=O)N2C1CN(CC2)S(=O)(=O)C3=CC=C(C=C3)F
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
3 sectionsContents
- Pharmacology
- Chemistry
- References
Unifiram (developmental code name DM-232) is an experimental drug. that has antiamnesic and other effects in animal studies with far greater potency than piracetam. A number of related compounds are known, such as sunifiram (DM-235) and sapunifiram (MN-19). Unifiram has two enantiomers, with the dextro form being the more active isomer. It has been shown to reduce the duration of hypnosis induced by pentobarbital, without impairing motor coordination. , no formal human studies with unifiram have been conducted. Unifiram is not patented and, despite the lack of human and long-term toxicity studies, it is commonly sold online.
==Pharmacology== Unifiram, as well as sunifiram, were assayed at a wide panel of sites, including the most important receptors, ion channels, and transporters, but showed no affinity for any of the sites. They specifically did not bind to the glutamate, GABA, serotonin, dopamine, adrenergic, histamine, acetylcholine, or opioid receptors at concentrations of up to 1 μM. In addition, the drugs were tested on recombinant AMPA receptors and showed no potentiation of the receptors, indicating that they do not act as AMPA receptor positive allosteric modulators. However, they were able to prevent the amnesia induced by the AMPA receptor antagonist NBQX in the passive avoidance test, suggesting that indirect/downstream AMPA receptor activation may be involved in their memory-enhancing effects.
Excerpted from Wikipedia’s “unifiram” article, available under the CC BY-SA 4.0 licence.