Medicinal chemistry of combretastatin A4: present and future directions

GC Tron, T Pirali, G Sorba, F Pagliai… - Journal of medicinal …, 2006 - ACS Publications
A growing solid tumor relies on a developing vasculature to meet its needs in terms of
oxygen, nutrients, depuration, etc. This implies that if the vascular bed that has developed …

Plant-based anticancer molecules: a chemical and biological profile of some important leads

V Srivastava, AS Negi, JK Kumar, MM Gupta… - Bioorganic & medicinal …, 2005 - Elsevier
A number of natural products, with diverse chemical structures, have been isolated as
anticancer agents. Several potential lead molecules such as camptothecin, vincristine …

Indole, a core nucleus for potent inhibitors of tubulin polymerization

A Brancale, R Silvestri - Medicinal research reviews, 2007 - Wiley Online Library
Microtubules are the basic components of cell structure, which take part in a wide number of
pivotal cellular functions. Drugs that are able to modulate the microtubule assembly either by …

Tubulin inhibitors targeting the colchicine binding site: a perspective of privileged structures

W Li, H Sun, S Xu, Z Zhu, J Xu - Future medicinal chemistry, 2017 - Taylor & Francis
The vital roles of microtubule in mitosis and cell division make it an attractive target for
antitumor therapy. Colchicine binding site of tubulin is one of the most important pockets that …

A common pharmacophore for a diverse set of colchicine site inhibitors using a structure-based approach

TL Nguyen, C McGrath, AR Hermone… - Journal of medicinal …, 2005 - ACS Publications
Modulating the structure and function of tubulin and microtubules is an important route to
anticancer therapeutics, and therefore, small molecules that bind to tubulin and cause …

Insights into drug discovery from natural products through structural modification

J Chen, W Li, H Yao, J Xu - Fitoterapia, 2015 - Elsevier
Natural products (NPs) have played a key role in drug discovery and are still a prolific
source of novel lead compounds or pharmacophores for medicinal chemistry …

Concise synthesis and structure− activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin …

JP Liou, YL Chang, FM Kuo, CW Chang… - Journal of medicinal …, 2004 - ACS Publications
The synthesis and study of the structure− activity relationships of two new classes of
synthetic antitubulin compounds based on 1-aroylindole and 3-aroylindole skeletons are …

[PDF][PDF] Combretastatin A-4 analogs as anticancer agents

A Chaudhary, SN Pandeya, P Kumar… - Mini reviews in …, 2007 - researchgate.net
Cornbretastatin A-4 (CA-4) is one of the most potent antinnitotic and antiangiogenic agents
of natural origin. It has displayed potent antitunnor effect in a wide variety of preclinical …

Development of combretastatins as potent tubulin polymerization inhibitors

SNA Bukhari, GB Kumar, HM Revankar, HL Qin - Bioorganic chemistry, 2017 - Elsevier
The combretastatins are isolated from South African tree combretum caffrum kuntze. The
lead compound combretastatin A-4 has displayed remarkable cytotoxic effect in a wide …

Pharmaceutical design of antimitotic agents based on combretastatins

HP Hsieh, JP Liou, N Mahindroo - Current pharmaceutical …, 2005 - ingentaconnect.com
The design of novel anticancer agents based on the combretastatins, a group of antimitotic
agents isolated from the bark of the South African willow tree Combretum caffrum Kuntz, is of …