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unifiram

Structure via PubChem · Public domain (PubChem)

EntityQ6590512· pop 5· linked from 517 articles

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 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

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 sections
Contents
  • 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.

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