Names | |
---|---|
IUPAC name (2S,6R,14S,E)-5-ethylidene-14-(hydroxymethyl)-3,14-dimethyl-2,3,4,5,6,7-hexahydro-1H-2,6-methanoazecinoindol-8(9H)-one | |
Other names 17-hydroxy-vobasan-3-one, | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
PubChem CID | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C20H24N2O2 |
Molar mass | 324.424 g·mol |
Melting point | 265°C (decomp.) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Affinine is a monoterpenoid indole alkaloid which can be isolated from plants of the genus Tabernaemontana. Structurally it can be considered a member of the vobasine alkaloid family and may be synthesized from tryptophan. Limited pharmacological testing has indicated that it may be an effective inhibitor of both acetylcholinesterase and butyrylcholinesterase.
See also
References
- ^ Weisbach, Jerry A.; Raffauf, Robert F.; Ribeiro, Oscar; Macko, Edward; Douglas, Bryce (April 1963). "Problems in chemotaxonomy I. Alkaloids ofPeschiera affinis". Journal of Pharmaceutical Sciences. 52 (4): 350–353. doi:10.1002/jps.2600520408. PMID 13999677.
- Monnerat, Cecilia Silva; Souza, Jucimar Jorgeane de; Mathias, Leda; Braz-Filho, Raimundo; Vieira, Ivo José C. (November 2005). "A new indole alkaloid isolated from Tabernaemontana hystrix steud (Apocynaceae)". Journal of the Brazilian Chemical Society. 16 (6b): 1331–1335. doi:10.1590/S0103-50532005000800004.
- Yang, Jie; Rallapalli, Sundari K.; Cook, James M. (February 2010). "The first enantiospecific total synthesis of the 3-oxygenated sarpagine indole alkaloids affinine and 16-epiaffinine, as well as vobasinediol and 16-epivobasinediol". Tetrahedron Letters. 51 (5): 815–817. doi:10.1016/j.tetlet.2009.12.002.
- Vieira, IJ; Medeiros, WL; Monnerat, CS; Souza, JJ; Mathias, L; Braz-Filho, R; Pinto, AC; Sousa, PM; Rezende, CM; Epifanio Rde, A (September 2008). "Two fast screening methods (GC-MS and TLC-ChEI assay) for rapid evaluation of potential anticholinesterasic indole alkaloids in complex mixtures". Anais da Academia Brasileira de Ciências. 80 (3): 419–26. doi:10.1590/S0001-37652008000300003. PMID 18797794.
This organic chemistry article is a stub. You can help Misplaced Pages by expanding it. |