Echitamidine

Echitamidine
Names
Other names
Methyl (19S)-19-hydroxy-2,16-didehydrocuran-17-oate
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C20H24N2O3/c1-11(23)13-10-22-8-7-20-14-5-3-4-6-15(14)21-18(20)17(19(24)25-2)12(13)9-16(20)22/h3-6,11-13,16,21,23H,7-10H2,1-2H3/t11-,12-,13-,16-,20?/m0/s1
    Key: DWLJVOJBWLYMJO-CZGIKHJPSA-N
  • C[C@@H]([C@@H]1CN2CCC34[C@@H]2C[C@@H]1C(=C3NC5=CC=CC=C45)C(=O)OC)O
Properties
C20H24N2O3
Molar mass 340.423 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

Echitamidine is an indole alkaloid isolated from Alstonia boonei.[1] Its laboratory synthesis has been reported.[2]

References

  1. ^ Bodnar, A.; d'Agostino, J. (1977). "IV therapy. Part one: Infection control". The Journal of Practical Nursing. 27 (8): 18–21. PMID 587160.
  2. ^ Kuehne, Martin E.; Xu, Feng; Brook, Christopher S. (1994). "Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. 6. Total Syntheses of (±)-Echitamidine, (±)-Alstogustine, (±)-19-epi-Alstogustine, and (±)-Akuammicine". The Journal of Organic Chemistry. 59 (25): 7803–7806. doi:10.1021/jo00104a042.
This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.