Recent advances of tubulin inhibitors targeting the colchicine binding site for cancer therapy

M Hawash - Biomolecules, 2022 - mdpi.com
Cancer accounts for numerous deaths each year, and it is one of the most common causes
of death worldwide, despite many breakthroughs in the discovery of novel anticancer …

An overview of tubulin inhibitors that interact with the colchicine binding site

Y Lu, J Chen, M Xiao, W Li, DD Miller - Pharmaceutical research, 2012 - Springer
Tubulin dynamics is a promising target for new chemotherapeutic agents. The colchicine
binding site is one of the most important pockets for potential tubulin polymerization …

[图书][B] Anticancer agents from natural products

GM Cragg, DGI Kingston, DJ Newman - 2005 - taylorfrancis.com
Plants, marine organisms, and microorganisms have evolved complex chemical defense
and signaling systems that are designed to protect them from predators and provide other …

Indole molecules as inhibitors of tubulin polymerization: potential new anticancer agents

SA Patil, R Patil, DD Miller - Future medicinal chemistry, 2012 - Taylor & Francis
Agents that interfere with tubulin function have a broad anti-tumor spectrum and they
represent one of the most significant classes of anticancer agents. In the past few years …

Discovery of 7-Hydroxy-6-methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan (BNC105), a Tubulin Polymerization Inhibitor with Potent Antiproliferative and …

BL Flynn, GS Gill, DW Grobelny… - Journal of medicinal …, 2011 - ACS Publications
A structure–activity relationship (SAR) guided design of novel tubulin polymerization
inhibitors has resulted in a series of benzo [b] furans with exceptional potency toward cancer …

Synthesis and evaluation of azetidinone analogues of combretastatin A-4 as tubulin targeting agents

NM O'Boyle, M Carr, LM Greene, O Bergin… - Journal of medicinal …, 2010 - ACS Publications
The synthesis and antiproliferative activity of a new series of rigid analogues of
combretastatin A-4 are described which contain the 1, 4-diaryl-2-azetidinone (β-lactam) ring …

Toward highly potent cancer agents by modulating the C-2 group of the arylthioindole class of tubulin polymerization inhibitors

G La Regina, R Bai, WM Rensen… - Journal of medicinal …, 2013 - ACS Publications
New arylthioindole derivatives having different cyclic substituents at position 2 of the indole
were synthesized as anticancer agents. Several compounds inhibited tubulin polymerization …

ZrCl4-Mediated Regio- and Chemoselective Friedel–Crafts Acylation of Indole

SK Guchhait, M Kashyap, H Kamble - The Journal of Organic …, 2011 - ACS Publications
An efficient method for regio-and chemoselective Friedel–Crafts acylation of indole using
acyl chlorides in the presence of ZrCl4 has been discovered. It minimizes/eliminates …

Acylation of indoles via photoredox catalysis: a route to 3-acylindoles

L Gu, C Jin, J Liu, H Zhang, M Yuan, G Li - Green Chemistry, 2016 - pubs.rsc.org
A visible-light-induced synthesis of 3-acylindoles from simple indoles and α-oxo acids at
room temperature has been discovered. The reaction tolerates a wide range of functional …

Synthesis of 3-Acylindoles by Visible-Light Induced Intramolecular Oxidative Cyclization of o-Alkynylated N,N-Dialkylamines

P Zhang, T Xiao, S Xiong, X Dong, L Zhou - Organic letters, 2014 - ACS Publications
A visible-light photoredox synthesis of 3-acylindoles through intramolecular oxidative
cyclization of o-alkynylated N, N-dialkylamines is developed. The reaction proceeds …