Phytogrowth-Inhibitory Lactones Derivatives of Glaucolide B

Author:

Barbosa Luiz Claúdio de A.1,Costa Adilson V.1,Piló-Veloso Dorila2,Lopes Joao Luiz C.3,Hernandez-Terrones Manuel G.4,King-Diaz Beatriz5,Lotina-Hennsen Blas6

Affiliation:

1. Departamento de Química, Universidade Federal de Vicosa, 36571-000, Vicosa - MG, Brazil

2. Departamento de Química, Universidade Federal de Minas Gerais, Belo Horizonte - MG, Brazil

3. Faculdade de Ciencias Farmaceuticas de Ribeirao Preto, USP, Sao Paulo - SP, Brazil

4. Instituto de Química, Universidade Federal de Uberlandia, Uberlandia - MG, Brazil

5. Departamento de Bioquímica, Facultad de Química, Universidad Nacional Autónoma de México, Cuidad Universitária, México D. F. 04510, México.

6. Departamento de Bioquímica, Facultad de Química, Universidad Nacional Autónoma de México, Cuidad Universitária, México D. F. 04510, México

Abstract

The sesquiterpene lactone glaucolide B (1), isolated from Vernonia fruticulosa (Asteraceae), was transformed into six lactones (2-7). The structures of the products were elucidated by spectroscopic analysis. A series of solutions of compounds 1-7, at 200 μᴍ, were tested on the germination and on the root and shoot growth of the dicotyledons Physalis ixocarpa and Trifolium alexandrinum and of the monocotyledons Lolium multiflorum and Amaranthus hypochondriacus. Lactone 5 exhibited clear selectivity towards dicotyledonous species at 200 μᴍ, with an average inhibition of 90% on the germination of P. ixocarpa. Lactones 1, 3 and 4 had a greater effect on root length of monocotyledonous species, inhibiting around 70% at 200 μᴍ in L. multiflorum. It seems that the diol function is required in lactones 4-6 to increase the activity, the polarity in the molecule might be required to reach its target.

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

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