Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/38794
Título: (R)-(−)-Aloesaponol III 8-Methyl Ether from Eremurus persicus: A Novel Compound against Leishmaniosis
Autor: Rossi, Daniela 
Ahmed, Karzan 
Gaggeri, Raffaella 
Della Volpe, Serena 
Maggi, Lauretta 
Mazzeo, Giuseppe 
Longhi, Giovanna 
Abbate, Sergio 
Corana, Federica 
Martino, Emanuela 
Machado, Marisa 
Varandas, Raquel 
Sousa, Maria 
Collina, Simona 
Palavras-chave: Leishmaniosis; Drug identification; Eremurus persicus; Plant extract; (R)-aloesaponol III-8 methyl ether
Data: 2017
Editora: MDPI
Título da revista, periódico, livro ou evento: Molecules
Volume: 22
Número: 4
Resumo: Leishmaniosis is a neglected tropical disease which affects several millions of people worldwide. The current drug therapies are expensive and often lack efficacy, mainly due to the development of parasite resistance. Hence, there is an urgent need for new drugs effective against Leishmania infections. As a part of our ongoing study on the phytochemical characterization and biological investigation of plants used in the traditional medicine of western and central Asia, in the present study, we focused on Eremurus persicus root extract in order to evaluate its potential in the treatment of leishmaniosis. As a result of our study, aloesaponol III 8-methyl ether (ASME) was isolated for the first time from Eremurus persicus root extract, its chemical structure elucidated by means of IR and NMR experiments and the (R) configuration assigned by optical activity measurements: chiroptical aspects were investigated with vibrational circular dichroism (VCD) and electronic circular dichroism (ECD) spectroscopies and DFT (density functional theory) quantum mechanical calculations. Concerning biological investigations, our results clearly proved that (R)-ASME inhibits Leishmania infantum promastigotes viability (IC50 73 µg/mL), inducing morphological alterations and mitochondrial potential deregulation. Moreover, it is not toxic on macrophages at the concentration tested, thus representing a promising molecule against Leishmania infections.
URI: https://hdl.handle.net/10316/38794
ISSN: 1420-3049
DOI: 10.3390/molecules22040519
10.3390/molecules22040519
Direitos: openAccess
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