The metabolism of tropinone in intact Datura innoxia plants
ME Landgrebe, E Leete
Index: Landgrebe, Mary E.; Leete, Edward Phytochemistry (Elsevier), 1990 , vol. 29, # 8 p. 2521 - 2524
Full Text: HTML
Citation Number: 16
Abstract
Abstract [methyl-14 C] Tropinone was synthesized by reaction of nortropinone with [14 C] methyl iodide. This labelled ketone was administered to intact Datura innoxia plants (3–4- month-old) by addition to the nutrient solution in which the roots were growing. The resultant alkaloids isolated from the plants after two days were radioactive with high specific incorporations: hyoscyamine (2.5%), scopolamine (7.3%). Degradations of these alkaloids ...
Related Articles:
[Berdini, Valerio; Cesta, Maria C; Curti, Roberto; D'Anniballe, Gaetano; Bello, Nicoletta Di; Nano, Giuseppe; Nicolini, Luca; Topai, Alessandra; Allegretti, Marcello Tetrahedron, 2002 , vol. 58, # 28 p. 5669 - 5674]
[Cheng, Jie; Xu, Liang; Stevens, Edwin D.; Trudell, Mark L.; Izenwasser, Sari; Wade, Dean Journal of Heterocyclic Chemistry, 2004 , vol. 41, # 4 p. 569 - 574]
[Journal of Medicinal Chemistry, , vol. 36, # 3 p. 343 - 352]
[Tetrahedron Letters, , vol. 30, # 30 p. 3977 - 3980]