lanuginosine/rak

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Cytotoxic Alkaloids from the Stem of Xylopia laevigata.

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Prijava / prijava

Xylopia laevigata (Annonaceae), known locally as "meiú" or "pindaíba", is widely used in folk medicine in Northeastern Brazil. In the present work, we performed phytochemical analyses of the stem of X. laevigata, which led to the isolation of 19 alkaloids: (-)-roemerine, (+)-anonaine, lanuginosine,

Cytotoxic and antiviral activities of aporphine alkaloids of Magnolia grandiflora L.

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Bioassay guided fractionation of the methanol extract of Magnolia grandiflora L. (Magnoliaceae) leaves led to the isolation and characterisation of four aporphine alkaloids, magnoflorine, lanuginosine, liriodenine and anonaine. The cytotoxicities of the pure compounds magnoflorine and lanuginosine

Cytotoxic C-benzylated chalcone and other constituents of Ellipeiopsis cherrevensis.

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A new natural C-benzylated chalcone, 2',4'-dihydroxy-3'-(2-hydroxybenzyl)-6'-methoxychalcone (2), along with two other flavonoids, tiliroside and kaempferol 3-O-rutinoside, and an oxoaporphine alkaloid, lanuginosine were isolated from the aerial parts of Ellipeiopsis cherrevensis (Annonaceae). Two

[Aporphine alkaloids from branches and leaves of Polyalthia nemoralis].

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OBJECTIVE To investigate the aporphine alkaloids in the branches and leaves of Polyalthia nemoralis. METHODS The compounds were isolated and purified by silica gel and Sephadex LH-20 column chromatographies. Their chemical structures were elucidated on the basis of physicochemical properties and

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Herbal & Natural Medicine

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