Anticancer Drug Design Using Scaffolds of β-Lactams, Sulfonamides, Quinoline, Quinoxaline and Natural Products. Drugs Advances in Clinical Trials
Authors: Balderas-Renteria, I.; Gonzalez-Barranco, P.; Garcia, A.; K. Banik, B.; Rivera, G.
Source: Current Medicinal Chemistry, Volume 19, Number 26, September 2012 , pp. 4377-4398(22)
Publisher: Bentham Science Publishers
Abstract:
Eleven years after the start of a new millennium characterized by amazing scientific development, the cure for cancer remains a major challenge for humanity. In this regard, scientific efforts have focused on the search for new therapeutic targets that involve specific recognition and stop the spread of cancer cells, as well as the development of new therapeutic options that show greater specificity and better therapeutic efficacy. This review includes recent published literature about new anticancer drug design using scaffolds of β-lactams, sulfonamides, quinoline, quinoxaline and natural products, and focuses on the structure-activity relationships of scaffolds that have been reported to potently inhibit cell growth of human tumor cell lines. It describes not only those synthetic or natural compounds aimed at specific molecular targets of cancer cells in vitro, but also compounds currently in clinical trials.Keywords: Cancer; drugs; lactams; natural products; quinoline; quinoxaline; sulfonamide; targets; clinical trials; anticancer
Document Type: Research article
DOI: http://dx.doi.org/10.2174/092986712803251593
Publication date: 2012-09-01
- Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews written by leaders in the field covering a range of the current topics in medicinal chemistry. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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- In this Subject: Pharmacology
- By this author: Balderas-Renteria, I. ; Gonzalez-Barranco, P. ; Garcia, A. ; K. Banik, B. ; Rivera, G.

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