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Article didn't say what kind of effects. Effects 1-3 in referenced article are all antagonistic to chemically induced amnesia.
Added study showing AMPA-r activation in the anti-amnesiac effects of sunifiram
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'''Sunifiram''' ('''DM-235''') is a [[piperazine]] derived [[research chemical]] which has anti-amnesiac effects in animal studies with significantly higher potency than [[piracetam]].<ref name=Gualtieri2016rev>{{cite journal | vauthors = Gualtieri F | title = Unifi nootropics from the lab to the web: a story of academic (and industrial) shortcomings | journal = Journal of Enzyme Inhibition and Medicinal Chemistry | volume = 31 | issue = 2 | pages = 187–94 | year = 2016 | pmid=25831025 | doi=10.3109/14756366.2015.1021252}}</ref>
'''Sunifiram''' ('''DM-235''') is a [[piperazine]] derived [[research chemical]] which has anti-amnesiac effects in animal studies with significantly higher potency than [[piracetam]].<ref name=Gualtieri2016rev>{{cite journal | vauthors = Gualtieri F | title = Unifi nootropics from the lab to the web: a story of academic (and industrial) shortcomings | journal = Journal of Enzyme Inhibition and Medicinal Chemistry | volume = 31 | issue = 2 | pages = 187–94 | year = 2016 | pmid=25831025 | doi=10.3109/14756366.2015.1021252}}</ref> Sunifiram is closely related to, and derived from, [[unifiram]]. The anti-amnesiac effect of both chemicals has been shown to involve AMPA-receptor activation.<ref>{{Cite journal
| last1 = Galeotti | first1 = N.
| last2 = Ghelardini | first2 = C.
| last3 = Pittaluga | first3 = A.
| last4 = Pugliese | first4 = A.
| last5 = Bartolini | first5 = A.
| last6 = Manetti | first6 = D.
| last7 = Romanelli | first7 = M.
| last8 = Gualtieri | first8 = F.
| title = AMPA-receptor activation is involved in the antiamnesic effect of DM 232 (unifiram) and DM 235 (sunifiram)
| journal = Naunyn-Schmiedeberg's archives of pharmacology
| volume = 368
| issue = 6
| pages = 538–545
| year = 2003
| pmid = 14600801
| doi = 10.1007/s00210-003-0812-6
}}</ref>


As of 2016 it had not been subjected to toxicology testing, nor to any human [[clinical trials]], and is not approved for use anywhere in the world.<ref name=Gualtieri2016rev/>
As of 2017 it had not been subjected to toxicology testing, nor to any human [[clinical trials]], and is not approved for use anywhere in the world.<ref name=Gualtieri2016rev/>


==References==
==References==

Revision as of 09:54, 7 March 2017

Sunifiram
Legal status
Legal status
  • US: Not FDA approved; unscheduled
Identifiers
  • 1-Benzoyl-4-propanoylpiperazine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H18N2O2
Molar mass246.304 g/mol g·mol−1
3D model (JSmol)
  • CCC(=O)N1CCN(CC1)C(=O)c2ccccc2
  • 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 ☒N
  • Key:DGOWDUFJCINDGI-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Sunifiram (DM-235) is a piperazine derived research chemical which has anti-amnesiac effects in animal studies with significantly higher potency than piracetam.[1] Sunifiram is closely related to, and derived from, unifiram. The anti-amnesiac effect of both chemicals has been shown to involve AMPA-receptor activation.[2]

As of 2017 it had not been subjected to toxicology testing, nor to any human clinical trials, and is not approved for use anywhere in the world.[1]

References

  1. ^ a b Gualtieri F (2016). "Unifi nootropics from the lab to the web: a story of academic (and industrial) shortcomings". Journal of Enzyme Inhibition and Medicinal Chemistry. 31 (2): 187–94. doi:10.3109/14756366.2015.1021252. PMID 25831025.
  2. ^ Galeotti, N.; Ghelardini, C.; Pittaluga, A.; Pugliese, A.; Bartolini, A.; Manetti, D.; Romanelli, M.; Gualtieri, F. (2003). "AMPA-receptor activation is involved in the antiamnesic effect of DM 232 (unifiram) and DM 235 (sunifiram)". Naunyn-Schmiedeberg's archives of pharmacology. 368 (6): 538–545. doi:10.1007/s00210-003-0812-6. PMID 14600801.

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