catharanthine/breast neoplasms

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NakalaMajaribio ya klinikiHati miliki

Chagua aina ya aina

5 matokeo

[Structural analysis of vinorelbine in solution determined by nuclear magnetic resonance spectrometry].

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Ingia / Ingia

An active partnership between the National Centre for Scientific Research (CNRS) and the laboratories Pierre Fabre is underpinning the development of a new molecule, vinorelbine, whose tartrate received marketing authorization in France in 1989, under the name of Navelbine. This medicine was first

Efficacy and tolerability of vinorelbine in the cancer therapy.

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Ingia / Ingia

Vinorelbine (VRN) is one of the most representative compounds of its class: the vinca alkaloids. VRN interferes with microtubule assembly. VRN shows a better therapeutic index than the parent compound vincristine and vinblastine probably because of its higher affinity for mitotic microtubules. VNR

The current and future place of vinorelbine in cancer therapy.

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Ingia / Ingia

Vinorelbine is a new semisynthetic vinca alkaloid that differs chemically from vinblastine by a substitution of the catharanthine moiety. The antitumour activity of vinorelbine against murine tumours, human malignant cell lines and human tumour xenografts in nude mice is evidence of its powerful

Vinorelbine: a new promising drug in Hodgkin's disease.

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Ingia / Ingia

Vinorelbine is a new semisynthetic vinca alkaloid that differs chemically from vinblastine by a substitution of the catharanthine moiety. The powerful cytostatic activity of vinorelbine against murine tumors, human malignant cell lines and human tumor xenografts in nude mice has been demonstrated.

Vinflunine: a new microtubule inhibitor agent.

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Ingia / Ingia

Vinflunine (Javlor) is the first fluorinated microtubule inhibitor belonging to the Vinca alkaloids family. Vinflunine is obtained by semisynthesis using superacidic chemistry to selectively introduce two fluorine atoms at the 20' position of the catharanthine moiety. This compound has been selected

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Herbal & Natural Medicine

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