3,3-Diisopentenyl-N-Methyl-2,4-Quinoldione from Esenbeckia Almawillia: The Antitumor Activity of this Alkaloid and its Derivatives

Author:

Nunes Fátima M.1,Barros-Filho Bartholomeu A.1,de Oliveira Maria C. F.1,de Mattos Marcos C.1,Andrade-Neto Manoel1,Barbosa Francisco G.1,Mafezoli Jair2,Montenegro Raquel C.3,Pessoa Cláudia3,de Moraes Manoel O.3,Costa-Lotufo Letícia V.3,Galetti Fabio C. S.4,Silva Celio L.4,De Souza Ana O.5

Affiliation:

1. Curso de Pós-graduação em Química Orgânica, Departamento de Química Orgânica e Inorgânica, Universidade Federal do Ceará, Campus do Pici, Caixa Postal 6044, Fortaleza-CE, 60455-970, Brazil

2. Curso de Farmácia, Universidade de Fortaleza, Av. Washington Soares, 1321, Cx. Postal 1258, Fortaleza-CE, 60.811-341, Brazil

3. Departamento de Fisiologia e Farmacologia, Universidade Federal do Ceará, Caixa Postal 3157, Fortaleza-CE, 60430-270, Brazil

4. Departamento de Bioquímica e Imunologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil

5. Laboratório de Bioquímica e Biofísica, Instituto Butantan, São Paulo, SP, Brazil

Abstract

n-Hexane, chloroform and ethyl acetate fractions obtained from methanol extracts of the wood and roots of Esenbeckia almawillia (Rutaceae) were tested against five tumor cells lines (HL-60, CEM, B-16, HCT-8 and MCF-7). The most active fractions were the less polar ones (IC50 from 1.7 to 5.3 μg/mL) and these were subjected to column chromatography, allowing the isolation of the alkaloid 3,3-diisopentenyl-N-methyl-2, 4-quinoldione (1) in high yields. Alkaloid 1 was bioassayed and gave an IC50 value in the range 9.2 to >25 μg/mL. Derivatives 2–12, obtained by chemical modifications of 1, were tested and lower IC50 values were found for compounds 4 (IC50 from 2.8 to 17.0 μg/mL), 10 (IC50 from 5.9 to 15.8 μg/mL) and 11 (IC50 from 6.7 to 14.8 μg/mL).

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

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