Tisopurine

Chemical compound
  • M04AA02 (WHO)
Identifiers
  • 1,2-Dihydro-4H-pyrazolo[3,4-d]pyrimidine-4-thione
CAS Number
  • 5334-23-6 checkY
PubChem CID
  • 667510
ChemSpider
  • 580886
UNII
  • 79F9I2R16M
KEGG
  • D07278 checkY
CompTox Dashboard (EPA)
  • DTXSID90201488 Edit this at Wikidata
ECHA InfoCard100.023.865 Edit this at WikidataChemical and physical dataFormulaC5H4N4SMolar mass152.18 g·mol−13D model (JSmol)
  • Interactive image
  • c1c2c([nH]n1)ncnc2S
InChI
  • InChI=1S/C5H4N4S/c10-5-3-1-8-9-4(3)6-2-7-5/h1-2H,(H2,6,7,8,9,10)
  • Key:PYAOPMWCFSVFOT-UHFFFAOYSA-N
  (verify)

Tisopurine (or thiopurinol) is a drug used in the treatment of gout in some countries.[1] It reduces uric acid production through inhibiting an early stage in its production.[2]

References

  1. ^ Dean BM, Perrett D, Simmonds HA, Grahame R (April 1974). "Thiopurinol: comparative enzyme inhibition and protein binding studies with allopurinol, oxipurinol and 6-mercaptopurine". British Journal of Clinical Pharmacology. 1 (2): 119–27. doi:10.1111/j.1365-2125.1974.tb00220.x. PMC 1402452. PMID 22454898.
  2. ^ Jawad AS (June 1987). "Alternatives to allopurinol". Annals of the Rheumatic Diseases. 46 (6): 493. doi:10.1136/ard.46.6.493-a. PMC 1002174. PMID 3632073.
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Receptor
(ligands)
P0 (adenine)
P1
(adenosine)
P2
(nucleotide)
P2X
(ATPTooltip Adenosine triphosphate)
P2Y
Transporter
(blockers)
CNTsTooltip Concentrative nucleoside transporters
ENTsTooltip Equilibrative nucleoside transporters
PMATTooltip Plasma membrane monoamine transporter
Enzyme
(inhibitors)
XOTooltip Xanthine oxidase
Others
Others
See also: Receptor/signaling modulators
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