Chemistry:Rhazinilam
From HandWiki
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| Preferred IUPAC name
(3aR)-3a-Ethyl-2,3,3a,4,5,7-hexahydroindolizino[8,1-ef][1]benzazonin-6(1H)-one | |
| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C19H22N2O | |
| Molar mass | 294.398 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 | |
Rhazinilam is an alkaloid first isolated in 1965 by Linde from the Melodinus australis plant. It was later isolated from the shrub Rhazya stricta as well as from other organisms.
Biological activity
Rhazinilam has activity similar to that of colchicine, taxol and vinblastine, acting as a spindle poison.[1]
Total synthesis
Rhazinilam was first synthesized in 1973 by Smith and coworkers, and multiple subsequent times.[2]
Trauner synthesis
Bowie, Alfred L.; Hughes, Chambers C.; Trauner, Dirk. "Concise Synthesis of (±)-Rhazinilam through Direct Coupling". Organic Letters 7 (23): 5207–5209. doi:10.1021/ol052033v. PMID 16268539.
References
- ↑ David, Bruno; Sévenet, Thierry; Thoison, Odile; Awang, Khalijah; Païs, Mary; Wright, Michel; Guénard, Daniel. "Hemisynthesis of rhazinilam analogues: structure - activity relationships on tubulin-microtubule system". Bioorganic & Medicinal Chemistry Letters 7 (17): 2155–2158. doi:10.1016/S0960-894X(97)00391-0.
- ↑ Ratcliffe, A.H.; Smith, G.F.; Smith, G.N.. "The synthesis of rhazinilam". Tetrahedron Letters 14 (52): 5179–5184. doi:10.1016/S0040-4039(01)87657-7.
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