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Total synthesis and anti-leishmanial activity of some curcumin analogues
Denise de Castro Ferreira Gomes1, Leila Vilela Alegrio, Leonor L Leon
1Universidade Federal Rural do Rio de Janeiro, Departamento de Química-Instituto de Ciências Exatas, Seropédica, RJ, Brazil.
Abstract:
Curcumin (1) an important yellow dye isolated from Curcuma longa rhizomes, exhibits a variety of pharmacological effects such as anti-inflammatory, antioxidant and antiviral activity. Ten curcuminoids (2-11) were synthesized by the condensation of 2,4-pentanedione with differently substituted benzaldehydes, using the boron complex approach, which avoided Knoevenagel condensation at C-3 of the diketone. The curcuminoids were assayed in vitro against Leishmania amazonensis promastigotes using pentamidine isethionate (CAS 140-64-7) as the reference drug. Compound (5) 1,7-bis-(2-hydroxy-4-methoxyphenyl)-1,6-heptadiene-3,5-dione) was the most effective.