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Toxopyrimidine

From Wikipedia, the free encyclopedia
Toxopyrimidine
Names
Preferred IUPAC name
(4-Amino-2-methylpyrimidin-5-yl)methanol
Other names
Pyramin[1]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.234.283Edit this at Wikidata
UNII
  • InChI=1S/C6H9N3O/c1-4-8-2-5(3-10)6(7)9-4/h2,10H,3H2,1H3,(H2,7,8,9)
    Key: VUTBELPREDJDDH-UHFFFAOYSA-N
  • Cc1ncc(c(n1)N)CO
Properties
C6H9N3O
Molar mass139.158 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Toxopyrimidine is avitamin B6 antagonist with potentconvulsant effects.[2][3]

See also

[edit]

References

[edit]
  1. ^Haughton BG, King HK (December 1958)."Toxo-pyrimidine phosphate as an inhibitor of bacterial enzyme systems that require pyridoxal phosphate".The Biochemical Journal.70 (4):660–5.doi:10.1042/bj0700660.PMC 1196724.PMID 13607425.
  2. ^Rindi G, Ferrari G (February 1959). "The gamma-aminobutyric acid and glutamic acid content of brains of rats treated with toxopyrimidine".Nature.183 (4661):608–9.Bibcode:1959Natur.183..608R.doi:10.1038/183608a0.PMID 13632808.S2CID 4200644.
  3. ^Rindi G, Perri V, Ventura U (April 1959). "Effect of toxopyrimidine on glutamic-decarboxylase and glutamic-oxalacetic transaminase of rat brain".Nature.183 (4668):1126–7.Bibcode:1959Natur.183.1126R.doi:10.1038/1831126a0.PMID 13657025.S2CID 4209134.

External links

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Animal toxins
Bacterial
Cyanotoxins
Plant toxins
Mycotoxins
Pesticides
Nerve agents
Bicyclic phosphates
Cholinergic neurotoxins
Psychoactive drugs
Other
GABA receptor antagonists
GABA synthesis inhibitors
Glycine receptor antagonists
Glutamate receptor agonists
Convulsantbarbiturates
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