Structure of malagashanine,a new alkaloid with chloroquine-potentiating action |
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Authors: | Mino R. Caira Philippe Rasoanaivo |
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Affiliation: | (1) Department of Chemistry, University of Cape Town, 7700 Rondebosch, South Africa;(2) Institut Malgache de Recherches Appliquées, B.P. 3833, 101 Antananarivo, Madagascar |
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Abstract: | ![]() The molecular structure of malagashanine (C23H30N2O4), a new alkaloid occurring in MadagascanStrychnos species and showing chloroquine-potentiating action, has been determined by single crystal X-ray diffraction. The crystals, in the form of a 1 1 acetone solvate, are monoclinic, space group P21, witha=10.328(2),b=10.554(6),c=11.490(5)Å, =96.67(2)0,Z=2. Refinement based on 3650 reflections measured at 294K yieldedR=0.045. The X-ray analysis shows that the ring system in malagashanine differs from that in alkaloids of the strychnobrasiline type in containing only five-and six-membered rings. Thermal analysis of the solvate indicates that the acetone molecules are firmly held in the crystal and the X-ray analysis reveals that they are trapped in crystal voids. Only van der Waals forces and C–H...O hydrogen bonds stabilize the crystal structure. |
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Keywords: | Alkaloid Strychnos acetone solvate |
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