dc.creator | Minteguiaga, Manuel | |
dc.creator | Torres, Ana María | |
dc.creator | Ricciardi, Gabriela Ana Leticia | |
dc.creator | Dellacassa, Eduardo Santiago | |
dc.creator | Catalán, César | |
dc.date.accessioned | 2022-08-18T13:59:11Z | |
dc.date.accessioned | 2023-06-16T00:36:03Z | |
dc.date.available | 2022-08-18T13:59:11Z | |
dc.date.available | 2023-06-16T00:36:03Z | |
dc.date.created | 2022-08-18T13:59:11Z | |
dc.date.issued | 2017 | |
dc.identifier | Minteguiaga, 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.identifier | http://repositorio.unne.edu.ar/handle/123456789/49897 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/6673496 | |
dc.description.abstract | Irregular 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.language | eng | |
dc.publisher | International Union of Pure and Applied Chemistry | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/2.5/ar/ | |
dc.rights | openAccess | |
dc.subject | Baccharis trimera | |
dc.subject | Irregular monoterpenes | |
dc.subject | Snake venom | |
dc.title | Semi-synthesis, structural elucidation and in-vitro anti-snake venom activity of irregular monoterpenes derivatives from Baccharis trimera (Asteraceae) | |
dc.type | Póster | |