Toxopyrimidine

Toxopyrimidine
Names
	Preferred IUPAC name (4-Amino-2-methylpyrimidin-5-yl)methanol
	Other names Pyramin
Identifiers
CAS Number	73-67-6;
3D model (JSmol)	Interactive image;
ChemSpider	756;
ECHA InfoCard	100.234.283
PubChem CID	777;
UNII	G62V17J09J;
CompTox Dashboard (EPA)	DTXSID80223275 ;
	InChI 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;
	SMILES Cc1ncc(c(n1)N)CO;
Properties
Chemical formula	C6H9N3O
Molar mass	139.158 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Toxopyrimidine is a vitamin B₆ antagonist with potent convulsant effects.^[2]^[3]

References

^ 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.
^ 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.
^ 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.

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Names


Preferred IUPAC name (4-Amino-2-methylpyrimidin-5-yl)methanol
Other names Pyramin^[1]
Identifiers
CAS Number	73-67-6
3D model (JSmol)	Interactive image
ChemSpider	756
ECHA InfoCard	100.234.283
PubChem CID	777
UNII	G62V17J09J
CompTox Dashboard (EPA)	DTXSID80223275
InChI 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
SMILES Cc1ncc(c(n1)N)CO
Properties
Chemical formula	C₆H₉N₃O
Molar mass	139.158 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references