dc.creatorMinteguiaga, Manuel
dc.creatorTorres, Ana María
dc.creatorRicciardi, Gabriela Ana Leticia
dc.creatorDellacassa, Eduardo Santiago
dc.creatorCatalán, César
dc.date.accessioned2022-08-18T13:59:11Z
dc.date.accessioned2023-06-16T00:36:03Z
dc.date.available2022-08-18T13:59:11Z
dc.date.available2023-06-16T00:36:03Z
dc.date.created2022-08-18T13:59:11Z
dc.date.issued2017
dc.identifierMinteguiaga, Manuel, et al., 2017. Semi-synthesis, structural elucidation and in-vitro anti-snake venom activity of irregular monoterpenes derivatives from baccharis trimera (Asteraceae). Sesión de póster presentada en IUPAC 49th General Assembly. 40ª Reunião Anual da Sociedade Brasileira de Química. São Paulo: International Union of Pure and Applied Chemistry.
dc.identifierhttp://repositorio.unne.edu.ar/handle/123456789/49897
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6673496
dc.description.abstractIrregular monoterpenes are rare natural products found mainly in the Asteraceae family, whose skeleton does not follow the Ruzicka rule, which establishes a head-to-tail bond between the isoprene units [1]. Of the different types of terpenoids with reordered skeleton, those with an o-menthane skeleton are very rare, with the most relevant members being piquerols A and B from Piqueria trinervia Cav. and carquejol from Baccharis trimera (Less.) DC. (synonym: B. genistelloides) [2] (Figure 1) both plants belonging to the Asteraceae.
dc.languageeng
dc.publisherInternational Union of Pure and Applied Chemistry
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsopenAccess
dc.subjectBaccharis trimera
dc.subjectIrregular monoterpenes
dc.subjectSnake venom
dc.titleSemi-synthesis, structural elucidation and in-vitro anti-snake venom activity of irregular monoterpenes derivatives from Baccharis trimera (Asteraceae)
dc.typePóster


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