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N-(Isobutyl)-3,4-methylenedioxy Cinnamoyl Amide
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The plant Zanthoxylum zanthoxyloides (Lam.) Zepern. & Timler is one of the most important medicinal species of the genus Zanthoxylum on the African continent. It is used in the treatment and management of parasitic diseases in sub-Saharan Africa. These properties have inspired scientists to investigate species within the genus for bioactive compounds. However, a study, which details a spectroscopic, spectrometric and bioactivity guided extraction and isolation of antiparasitic compounds from the genus Zanthoxylum is currently non-existent. Tortozanthoxylamide (1), which is a derivative of the known compound armatamide was isolated from Z. zanthoxyloides and the full structure determined using UV, IR, 1D/2D-NMR and high-resolution liquid chromatography tandem mass spectrometry (HRESI-LC-MS) data. When tested against Trypanosoma brucei subsp. brucei, the parasite responsible for animal African trypanosomiasis in sub-Saharan Africa, 1 (IC50 7.78 µM) was just four times less active than the commercially available drug diminazene aceturate (IC50 1.88 µM). Diminazene aceturate is a potent drug for the treatment of animal African trypanosomiasis. Tortozanthoxylamide (1) exhibits a significant antitrypanosomal activity through remarkable alteration of the cell cycle in T. brucei subsp. brucei, but it is selectively non-toxic to mouse macrophages RAW 264.7 cell lines. This suggests that 1 may be considered as a scaffold for the further development of natural antitrypanosomal compounds.
Title: N-(Isobutyl)-3,4-methylenedioxy Cinnamoyl Amide
Description:
The plant Zanthoxylum zanthoxyloides (Lam.
) Zepern.
& Timler is one of the most important medicinal species of the genus Zanthoxylum on the African continent.
It is used in the treatment and management of parasitic diseases in sub-Saharan Africa.
These properties have inspired scientists to investigate species within the genus for bioactive compounds.
However, a study, which details a spectroscopic, spectrometric and bioactivity guided extraction and isolation of antiparasitic compounds from the genus Zanthoxylum is currently non-existent.
Tortozanthoxylamide (1), which is a derivative of the known compound armatamide was isolated from Z.
zanthoxyloides and the full structure determined using UV, IR, 1D/2D-NMR and high-resolution liquid chromatography tandem mass spectrometry (HRESI-LC-MS) data.
When tested against Trypanosoma brucei subsp.
brucei, the parasite responsible for animal African trypanosomiasis in sub-Saharan Africa, 1 (IC50 7.
78 µM) was just four times less active than the commercially available drug diminazene aceturate (IC50 1.
88 µM).
Diminazene aceturate is a potent drug for the treatment of animal African trypanosomiasis.
Tortozanthoxylamide (1) exhibits a significant antitrypanosomal activity through remarkable alteration of the cell cycle in T.
brucei subsp.
brucei, but it is selectively non-toxic to mouse macrophages RAW 264.
7 cell lines.
This suggests that 1 may be considered as a scaffold for the further development of natural antitrypanosomal compounds.
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