Drug intelligence / Profile preview

avanbulin

Development stage
Unknown
Lead developer
Glioblastoma Foundation
Modality
Prodrugs/Conditional Activator Small Molecules → Small Molecules, Multivalent & Scaffold-Based Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral (as Prodrug Lisavanbulin), Intravenous (preclinical/experimental)
01

Overview

Avanbulin (BAL27862) is a novel synthetic small molecule that acts as a potent microtubule-destabilizing agent by binding to the colchicine site on tubulin. It inhibits tubulin polymerization, disrupts the microtubule network essential for cell division, and induces apoptosis in cancer cells. Avanbulin demonstrates activity against tumor models resistant to standard microtubule-targeting agents such as taxanes and vinca alkaloids. The drug has been shown to overcome resistance mediated by P-glycoprotein overexpression and various tubulin modifications. Its unique mechanism of action results in distinct effects on microtubule organization compared to other agents in its class[1][2][4][6][9]. Avanbulin is the active moiety of lisavanbulin (BAL101553), an orally available prodrug developed for clinical use[3][5][7].

Other names
avanbulinBAL27862BAL-27862BAL 27862
02

Targets

TUBB (Tubulin (alpha and beta subunits))

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