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Synthesis and structure–activity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors
- Source :
- Bioorganic & Medicinal Chemistry Letters. 15:5154-5159
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- A novel triazole-containing chemical series was shown to inhibit tubulin polymerization and cause cell cycle arrest in A431 cancer cells with EC(50) values in the single digit nanomolar range. Binding experiments demonstrated that representative active compounds of this class compete with colchicine for its binding site on tubulin. The syntheses and structure-activity relationship studies for the triazole derivatives are described herein.
- Subjects :
- Cell cycle checkpoint
Stereochemistry
Clinical Biochemistry
Pharmaceutical Science
Antineoplastic Agents
macromolecular substances
Microtubules
Biochemistry
Chemical synthesis
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
Tumor Cells, Cultured
Humans
Colchicine
Structure–activity relationship
Binding site
Molecular Biology
Molecular Structure
biology
Organic Chemistry
1,2,4-Triazole
Triazoles
Tubulin Modulators
Tubulin
Epidermoid carcinoma
chemistry
biology.protein
Molecular Medicine
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....6565f9e235a9b3bc40e1659b52b776c9
- Full Text :
- https://doi.org/10.1016/j.bmcl.2005.08.056