Póster
Semi-synthesis, structural elucidation and in-vitro anti-snake venom activity of irregular monoterpenes derivatives from Baccharis trimera (Asteraceae)
Fecha
2017Registro en:
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.
Autor
Minteguiaga, Manuel
Torres, Ana María
Ricciardi, Gabriela Ana Leticia
Dellacassa, Eduardo Santiago
Catalán, César
Institución
Resumen
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.