Inhibitors of tubulin polymerization: Synthesis and biological evaluation of hybrids of vindoline, anhydrovinblastine and vinorelbine with thiocolchicine, podophyllotoxin and baccatin III

Bioorganic & Medicinal Chemistry
2008.0

Abstract

A series of novel hybrid compounds obtained by the attachment of anhydrovinblastine, vinorelbine, and vindoline to thiocolchicine, podophyllotoxin, and baccatin III are described. Two types of diacyl spacers are introduced. The influence of the hybrid compounds on tubulin polymerization is reported. The results highlight the importance of the length of the spacer. Immunofluorescence microscopy and flow cytometry measurements that compound with the best in vitro activity could disrupt microtubule networks in cell and prevent the formation of the proper spindle apparatus, thereby causing cell cycle arrest in the G2/M phase. The newly synthesized compounds were tested in the human lung cancer cell line A549.

Knowledge Graph

Similar Paper

Inhibitors of tubulin polymerization: Synthesis and biological evaluation of hybrids of vindoline, anhydrovinblastine and vinorelbine with thiocolchicine, podophyllotoxin and baccatin III
Bioorganic & Medicinal Chemistry 2008.0
Synthesis and biological evaluation of novel anticancer bivalent colchicine–tubulizine hybrids
Bioorganic & Medicinal Chemistry 2012.0
Synthesis and Biological Evaluation of Vinca Alkaloids and Phomopsin Hybrids
Journal of Medicinal Chemistry 2009.0
Synthesis of tetrazole–isoxazoline hybrids as a new class of tubulin polymerization inhibitors
MedChemComm 2012.0
Synthesis and biological evaluation of podophyllotoxin congeners as tubulin polymerization inhibitors
Bioorganic & Medicinal Chemistry 2014.0
Design, synthesis and biological evaluation of 2-phenylquinoline-4-carboxamide derivatives as a new class of tubulin polymerization inhibitors
Bioorganic & Medicinal Chemistry 2017.0
Design, synthesis and biological evaluation of millepachine derivatives as a new class of tubulin polymerization inhibitors
Bioorganic & Medicinal Chemistry 2013.0
Synthesis and biological evaluation of a series of podophyllotoxins derivatives as a class of potent antitubulin agents
Bioorganic & Medicinal Chemistry 2012.0
9-Benzylidene-naphtho[2,3-b]thiophen-4-ones as Novel Antimicrotubule AgentsSynthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization
Journal of Medicinal Chemistry 2006.0
Synthesis and biological evaluation of 4-aza-2,3-dihydropyridophenanthrolines as tubulin polymerization inhibitors
Bioorganic & Medicinal Chemistry Letters 2014.0