Jump to content
Wikipedia The Free Encyclopedia

Ungiminorine

From Wikipedia, the free encyclopedia
Ungiminorine
Names
IUPAC name
(1S,16R,17R,18S,19S)-17-methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,14-tetraene-16,18-diol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • InChI=1S/C17H19NO5/c1-21-17-15(19)9-2-3-18-6-8-4-11-12(23-7-22-11)5-10(8)13(14(9)18)16(17)20/h2,4-5,13-17,19-20H,3,6-7H2,1H3/t13-,14+,15+,16-,17-/m0/s1
    Key: ZQLQBAUVRGDBJL-BIVLZKPYSA-N
  • InChI=1/C17H19NO5/c1-21-17-15(19)9-2-3-18-6-8-4-11-12(23-7-22-11)5-10(8)13(14(9)18)16(17)20/h2,4-5,13-17,19-20H,3,6-7H2,1H3/t13-,14+,15+,16-,17-/m0/s1
    Key: ZQLQBAUVRGDBJL-BIVLZKPYBI
  • CO[C@@H]1[C@H]([C@@H]2[C@H]3C(=CCN3CC4=CC5=C(C=C24)OCO5)[C@H]1O)O
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Ungiminorine is an acetylcholinesterase inhibitor isolated from Narcissus .[1]

References

[edit ]
  1. ^ Ingkaninan, K.; Hazekamp, A.; de Best, C. M.; Irth, H.; Tjaden, U. R.; van der Heijden, R.; van der Greef, J.; Verpoorte, R. (June 2000). "The application of HPLC with on-line coupled UV/MS-biochemical detection for isolation of an acetylcholinesterase inhibitor from narcissus 'Sir Winston Churchill'". Journal of Natural Products. 63 (6): 803–806. doi:10.1021/np9905719. ISSN 0163-3864. PMID 10869205.
Enzyme
(modulators)
ChAT Tooltip Choline acetyltransferase
AChE Tooltip Acetylcholinesterase
BChE Tooltip Butyrylcholinesterase
Transporter
(modulators)
CHT Tooltip Choline transporter
VAChT Tooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers
Stub icon

This organic chemistry article is a stub. You can help Wikipedia by expanding it.

AltStyle によって変換されたページ (->オリジナル) /