Drug intelligence / Profile preview

vindesine

Development stage
Phase 4
Lead developer
Eli Lilly
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

Vindesine is a semisynthetic vinca alkaloid derived from vinblastine and the plant Catharanthus roseus. It acts as an antimitotic chemotherapy agent by binding to β-tubulin subunits of microtubules at the so-called "vinca site," inhibiting microtubule dynamics. This leads to mitotic arrest in metaphase and subsequent cell death. Vindesine is cell cycle phase-specific (S phase) and is used primarily for treating various malignancies including acute lymphocytic leukemia (ALL), lymphoma (including Hodgkin's disease), melanoma, breast cancer, and non-small cell lung cancer. Major side effects include myelosuppression and neurotoxicity.

Brand names
Eldisine
Other names
desacetylvinblastine amidevindesinavindesinumvindesine sulfate
02

Targets

TUBB (Tubulin (alpha and beta subunits))

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