Antitumor agents. 89. Psychorubrin, a new cytotoxic naphthoquinone from Psychotria rubra and its structure-activity relationships
- 1 November 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 30 (11) , 2005-2008
- https://doi.org/10.1021/jm00394a013
Abstract
A new naphthoquinone, isolated from the alcoholic extract of Psychotria rubra, exhibited significant cytotoxicity in the KB cell assay (ED50 = 3.0 .mu.g/mL). Spectral data was used to assign the structure of psychorubrin as 2. Naphthoquinone derivatives 6, 8, 13, and 14 were prepared and exhibited superior cytotoxic activity to that of psychorubrin. All were potential Michael acceptors whose conjugation has been extended. However, when a hydrophilic hydroxy group was present in such compounds, reduced in vitro activity was observed.This publication has 2 references indexed in Scilit:
- Plant Anticancer Agents. XII. Isolation and Structure Elucidation of New Cytotoxic Quinones From Tabebuia cassinoidesJournal of Natural Products, 1982
- Antitumor agents. 44. Bis(helenalinyl) esters and related derivatives as novel potent antileukemic agentsJournal of Medicinal Chemistry, 1981