| Literature DB >> 24768284 |
Jean Paulo de Andrade1, Ying Guo2, Mercè Font-Bardia3, Teresa Calvet4, Jullie Dutilh5, Francesc Viladomat2, Carles Codina2, Jerald J Nair2, Jose A Silveira Zuanazzi6, Jaume Bastida7.
Abstract
An ongoing search for alkaloids in the Amaryllidaceae species using GC-MS resulted in the identification of two crinine-type alkaloids, aulicine (1) and 3-O-methyl-epimacowine, (2) from the indigenous Brazilian species Hippeastrum aulicum and Hippeastrum calyptratum, respectively. In addition, two alkaloids, 11-oxohaemanthamine (3) and 7-methoxy-O-methyllycorenine (4) were both isolated from H. aulicum. Furthermore, we provide here complete NMR spectroscopic data for the homolycorine analogues nerinine (5) and albomaculine (6). The absolute stereochemistry of the 5,10b-ethano bridge in the crinine variants was determined by circular dichroism and X-ray crystallographic analysis, thus presenting the first direct evidence for the presence of crinine-type alkaloids in the genus Hippeastrum.Entities:
Keywords: Alkaloid; Amaryllidaceae; Circular dichroism; Crinine-type; Hippeastrum; X-ray crystallography
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Year: 2014 PMID: 24768284 DOI: 10.1016/j.phytochem.2014.03.007
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072