Vinburnine

Chemical compound
  • C04AX17 (WHO)
Identifiers
  • (3α,16α)-14,15-Dihydroeburnamenin-14-one
CAS Number
  • 4880-88-0 checkY
PubChem CID
  • 71203
IUPHAR/BPS
  • 345
ChemSpider
  • 64339 ☒N
UNII
  • G54D0HMY25
KEGG
  • D08676 checkY
ChEMBL
  • ChEMBL1892145 ☒N
CompTox Dashboard (EPA)
  • DTXSID6045119 Edit this at Wikidata
ECHA InfoCard100.023.172 Edit this at WikidataChemical and physical dataFormulaC19H22N2OMolar mass294.398 g·mol−13D model (JSmol)
  • Interactive image
  • CC[C@@]12CCCN3[C@@H]1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2
InChI
  • InChI=1S/C19H22N2O/c1-2-19-9-5-10-20-11-8-14-13-6-3-4-7-15(13)21(16(22)12-19)17(14)18(19)20/h3-4,6-7,18H,2,5,8-12H2,1H3/t18-,19+/m1/s1 ☒N
  • Key:WYJAPUKIYAZSEM-MOPGFXCFSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Vinburnine (or eburnamonine, Vincamone) is a vasodilator. Vincamone is a vinca alkaloid and a metabolite of vincamine.[1]

References

  1. ^ Vereczkey L, Tamás J, Czira G, Szporny L (1980). "Metabolism of vincamine in the rat in vivo and in vitro". Arzneimittel-Forschung. 30 (11): 1860–5. PMID 7192994.
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CARTooltip Constitutive androstane receptor
PXRTooltip Pregnane X receptor
See also
Receptor/signaling modulators
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