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Vinca Alkaloids

2000
Abstract Vincristine (VCR) and vinblastine (VBL), derivatives of the periwinkle plant (Vinca rosea), are important chemotherapeutic agents with similar neurotoxic actions. VCR, the subject here, is far more widely used than VBL and has Iqbal Z, Ochs S (1980) Uptake of Vinca alkaloids into mammalian nerve and its subcellular components.
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Radioimmunoassays for the vinca alkaloids, vinblastine and vincristine

Analytical Biochemistry, 1979
Abstract Radioimmunoassays for the chemotherapeutic alkaloids, vinblastine (VLB) and vincristine (VCR) were developed that could determine less than 1 pmol of each compound in the homologous hapten-antibody reaction. The anti-VCR serum bound VCR 200 times more effectively than VLB, demonstrating a high specificity in spite of the structural ...
J J, Langone   +2 more
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Plant Alkaloids: The Vinca Alkaloids

1989
Although a large number of compounds from a wide variety of plants have been tested for antitumor activity, none has played a more vital role in cancer chemotherapy than the vinca alkaloids. These compounds are present in minute quantities in the plant Catharanthus roseus G. Don (Vinca rosea Linn.), commonly called the periwinkle.
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Vinca alkaloids

Chemistry of Natural Compounds, 1977
V. M. Malikov, S. Yu. Yunusov
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[Vinca alkaloid and MDR1].

Gan to kagaku ryoho. Cancer & chemotherapy, 2008
Vinca alkaloids inhibit microtubule formation by binding to tubulin. There are four clinically available vinca alkaloids including vincristine, vinblastine, vindesine, and vinorelbine. P-glycoprotein(P-gp)is the one of the efflux adenosine triphosphate(ATP)-binding cassette family transporters and is the encoded product of MDR1 gene.
Nagio, Takigawa, Mitsune, Tanimoto
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The Vinca Alkaloids

1964
N, NEUSS   +3 more
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New Anticancer Vinca Alkaloids in the Last Decade - A Mini-Review

Current Organic Chemistry, 2021
Szabolcs Mayer   +2 more
exaly  

Vinca Alkaloids and Colchicine

1975
The vinca alkaloids and the colchicine derivatives, although of widely disparate chemical structure, may be considered to constitute a single class of agents in view of the many similarities in their biochemical and biological actions, most notably in their ability to produce metaphase arrest.
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