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leurosine/vinca

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ČlankiKliničnih preskušanjPatenti
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Clinical trials with leurosine methiodide, an alkaloid from Vinca rosea Linn.

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A note on several new alkaloids from Vinca rosea Linn. I. Leurosine, virosine, perivine.

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STUDIES ON CATHARANTHUS LANCEUS (VINCA LANCEA). I. ISOLATION OF LEUROSINE, PERIVINE, AND YOHIMBINE.

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Antitumor principles derived from Vinca rosea Linn. I. Vincaleukoblastine and leurosine.

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The Vinca alkaloid vinblastine causes dose-dependent inhibition of malondialdehyde formation and aggregation in activated human platelets as a result of inhibition of arachidonic acid metabolism via the thromboxane pathway (Brammer, J.P., Kerecsen, L. and Maguire, M.H. (1982) Eur. J. Pharmacol. 81,
The bisindole alkaloids vinblastine, vincristine, and N-formyl-leurosine were nitrated and subsequently converted to amino derivatives. In the case of compounds 5e and 5b cytotoxic activity has been found for non-small cell lung cancer and breast cancer in the concentration range tested

The mode of action of Vinca alkaloids.

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P388 leukemia-bearing mice were given a single i.p. injection of [14C]-vincristine and the levels of radioactivity in the tumors and host tissues were determined as a function of time. The highest levels of radioactivity were found in the gallbladder followed by the tumor, spleen and liver,
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