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Synthetic and Structure-Activity Relationship of Insecticidal Bufadienolides

Synthetic and Structure-Activity Relationship of Insecticidal Bufadienolides
Ace Tatang Hidayat, Achmad Zainuddin, Danar Dono, Wawan Hermawan, Hideo Hayashi, Unang Supratman
Universitas Padjadjaran, Natural Product Communications Vol. 9 (7) 2014
Bahasa Inggris
Universitas Padjadjaran, Natural Product Communications Vol. 9 (7) 2014
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A new synthetic analog of bufadienolide, methyl isobryophyllinate A (1), and a known synthetic analog, methyl isobersaldegenate-1,3,5-orthoacetate (2), were obtained by methanolysis of bryophyllin A (3) and bersaldegenin-1,3,5-orthoacetate (5) in basic solution. Structure-insecticidal activity relationship studies revealed both orthoacetate and ?-pyrone moieties seemed to be essential structural elements for exhibiting insecticidal activity, whereas oxygenated substituents in the C ring enhanced the insecticidal activity against the third instar larvae of silkworm (Bombyx mori).

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