9 methoxyellipticine/ochrosia

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Alkaloids of Ochrosia maculata Jacq. (Ochrosia borbonica Gmel.). Isolation of the alkaloids and study of the antitumor properties of 9-methoxyellipticine.

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Alkaloids from the Australian rainforest tree Ochrosia moorei.

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High-throughput screening of a plant and marine invertebrate extract library to find natural products that down-regulate expression of pro-inflammatory genes associated with the glucocorticoid receptor ligand complex led to the identification of bioactive CH2Cl 2 extracts from stems and leaves of

New indole alkaloids from the roots of Ochrosia acuminata.

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Two new indole alkaloids, polyneuridine-N-oxide (1) and 17-hydroxy-10-methoxy-yohimbane (2), together with seven known alkaloids were isolated from the roots of Ochrosia acuminata collected in Savu, Indonesia. 9-Methoxyellipticine (3) and ellipticine (4) were responsible for the antitumor activities

Pyridocarbazole alkaloids from Ochrosia borbonica: lipid-lowering agents inhibit the cell proliferation and adipogenesis of 3T3-L1 adipocyte via intercalating into supercoiled DNA.

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Bioassay-guided fractionation of an ethanolic extract of Ochrosia borbonica led to the isolation of two known pyridocarbazole alkaloids, ellipticine (1) and 9-methoxyellipticine (2), and six known monoterpenoid indole alkaloids (3-8). Lipid-lowering assay in 3T3-L1 cell model revealed that 1 and 2

Alkaloid Production by Ochrosia elliptica Cell Suspension Cultures.

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Ochrosia elliptica cell suspension cultures were obtained from callus cultures using an original «cell washing technique». These suspensions accumulated ellipticine, 9-methoxyellipticine, elliptinine, isoreserpiline, and reserpiline (a new alkaloid for this species) during the stationary growth

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