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Why not share! They can be classified based on the pathway by which they are synthesized [ 24 ]. Additionally, a simple classification includes three main groups: terpenoids polymeric isoprene derivatives and biosynthesized from acetate via the mevalonic acid pathway , phenolics biosynthesized from shikimate pathways, containing one or more hydroxylated aromatic rings and the extremely diverse alkaloids non-protein nitrogen-containing compounds, biosynthesized from amino acids such as tyrosine, with a long history in medication [ 24 , 25 ].
Several new cytotoxic secondary metabolites are isolated from plants each year and constitute a source of new possibilities to explore in order to fight against cancerous diseases. Although some natural compounds have unique anticancer effects, their use in clinical practice is not possible due to their physico-chemical properties e.
On the other hand, plant occurring secondary metabolites often can be excellent leads for drug development.
Thus, modifying the chemical structure of these more promising compounds is one strategic way to increase their anticancer action and selectivity, improve their absorption, distribution, metabolism and excretion properties and decrease their toxicity and side effects [ 26 , 27 ]. Herein we will present the most significant achievements in the area of plant secondary metabolites, some already in clinical use and others in clinical trials as anticancer agents, as well as their most efficient derivatives obtained by structural modifications.
Metabolites Used in Cancer Therapy During the last few decades, a wide range of cytotoxic agents was discovered from plants, but very few of these managed to reach clinical use after successfully running through the entire long, selective, expensive and bureaucratic process from their chemical identification to their effectiveness in therapeutic cancer treatment.
Each of these compounds has their histories of success and limitations, which has been told by many authors and which are hereinafter counted in a historical, molecular, pharmaceutical and clinical point of view.
Vincristine Vincristine 1 has a non-symmetrical dimeric structure, composed of a two indole-type nucleus linked by a carbon—carbon bond, the vindoline portion and the catharanthine type portion Figure 1. In fact, it was one of the first plant-derived anticancer agents approved by this agency [ 19 ].
It is a naturally-occurring alkaloid extracted from the leaves of Catharanthus roseus L. Don formerly Vinca rosea L. Its incorporation in the treatment regimen increases the survival rate to eighty percent [ 28 ].
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Advanced embedding details, examples, and help! Publication date Topics Cancer , Cancer , Cancer. Publisher New York: Collection inlibrary ; printdisabled ; internetarchivebooks ; delawarecountydistrictlibrary ; china ; americana. Digitizing sponsor Internet Archive.
Contributor Internet Archive. Language English. Bookplateleaf