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Vinervine information


Vinervine
Names
IUPAC name
Methyl (19E)-12-hydroxy-2,16-didehydrocur-19-en-17-oate
Identifiers
CAS Number
  • 1963-86-6 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:70500
ChemSpider
  • 65322594
PubChem CID
  • 6875257
UNII
  • QJ6XQD4UFS checkY
CompTox Dashboard (EPA)
  • DTXSID301140692 Edit this at Wikidata
InChI
  • InChI=1S/C20H22N2O3/c1-3-11-10-22-8-7-20-13-5-4-6-14(23)17(13)21-18(20)16(19(24)25-2)12(11)9-15(20)22/h3-6,12,15,21,23H,7-10H2,1-2H3/b11-3-/t12-,15-,20+/m0/s1
    Key: FAJVFJABOWWACZ-GGGKWMOSSA-N
SMILES
  • C/C=C\1/CN2CC[C@@]34[C@@H]2C[C@@H]1C(=C3NC5=C4C=CC=C5O)C(=O)OC
Properties
Chemical formula
C24H39NO7
Molar mass 453.576 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

Vinervine is a monoterpene indole alkaloid of the Vinca sub-group. It is a derivative of akuammicine, with one additional hydroxy (OH) group in the indole portion, hence it is also known as 12-hydroxyakuammicine.

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Vinervine

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Vinervine is a monoterpene indole alkaloid of the Vinca sub-group. It is a derivative of akuammicine, with one additional hydroxy (OH) group in the indole...

Word Count : 547

Isovoacangine

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pachysiphon and Tabernaemontana divaricata. Voacangine Tabernanthine Ibogaline Vinervine Danieli B, Palmisano G (January 1987). "Alkaloids from Tabernaemontana...

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Akuammicine

Last Update:

glucose uptake and be a κ- and μ-opioid receptor agonist. Ajmalicine Vinervine, the 12-hydroxy derivative Robinson, Robert; Thomas, A. F. (1955). "The...

Word Count : 829

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