Synthesis and Biological Evaluation of Benzo[b]furans as Inhibitors of Tubulin Polymerization and Inducers of Apoptosis. Issue 1 (7th November 2013)

• Record Type: Journal Article
• Authors: Kamal, Ahmed; Reddy, N. V. Subba; Nayak, V. Lakshma; Reddy, V. Saidi; Prasad, B.; Nimbarte, Vijaykumar D.; Srinivasulu, Vunnam; Vishnuvardhan, M. V. P. S.; Reddy, C. Suresh
• Is Part Of: ChemMedChem. Volume 9:Issue 1(2014:Jan.)
• Page Start: 117
• Page End: 128
• Publication Date: 2013-11-07
• Subjects: Pharmaceutical chemistry -- Periodicals; 615.19005
• DOI: 10.1002/cmdc.201300366
• Languages: English
• ISSNs: 1860-7179

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A series of benzo[<italic>b</italic>]furans was synthesized with modification at the 5‐position of the benzene ring by introducing C‐linked substituents (aryl, alkenyl, alkynyl, etc.). These compounds were evaluated for their antiproliferative activities, inhibition of tubulin polymerization, and cell‐cycle effects. Some compounds in this series displayed excellent activity in the nanomolar range against lung cancer (A549) and renal cell carcinoma (ACHN) cancer cell lines. (6‐Methoxy‐5‐((4‐methoxyphenyl)ethynyl)‐3‐methylbenzofuran‐2‐yl)(3, 4, 5‐trimethoxyphenyl)methanone (<bold>26</bold>) and (<italic>E</italic>)‐3‐(6‐methoxy‐3‐methyl‐2‐(1‐(3, 4, 5‐trimethoxyphenyl)vinyl)benzofuran‐5‐yl)prop‐2‐en‐1‐ol (<bold>36</bold>) showed significant activity in the A549 cell line, with IC<sub>50</sub> values of 0.08 and 0.06 μ<sc>M</sc>, respectively. G<sub>2</sub>/M cell‐cycle arrest and subsequent apoptosis was observed in the A549 cell line after treatment with these compounds. The most active compound in this series, <bold>36</bold>, also inhibited tubulin polymerization with a value similar to that of combretastatin A‐4 (1.95 and 1.86 μ<sc>M</sc>, respectively). Furthermore, detailed biological studies such as Hoechst 33258 staining, DNA fragmentation and caspase‐3 assays, and western blot analyses with the pro‐apoptotic protein Bax and the anti‐apoptotic protein Bcl‐2 also suggested that these compounds induce cell death by apoptosis. Molecular docking studies indicated that compound <bold>36</bold> interacts and binds efficiently with the tubulin protein.</p> </abstract>