Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

Echitamidine

From Wikipedia, the free encyclopedia
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).

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

References

[edit]
  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.