A perspective on the role of quantitative structure-activity and structure-property relationships in herbicide discovery

2012 ◽  
Vol 68 (4) ◽  
pp. 513-518 ◽  
Author(s):  
Robert D Clark
2007 ◽  
Vol 62 (22) ◽  
pp. 6222-6233 ◽  
Author(s):  
Mordechai Shacham ◽  
Olaf Kahrs ◽  
Georgi St. Cholakov ◽  
Roumiana P. Stateva ◽  
Wolfgang Marquardt ◽  
...  

2019 ◽  
Vol 18 (13) ◽  
pp. 1796-1814 ◽  
Author(s):  
Sk. Abdul Amin ◽  
Nilanjan Adhikari ◽  
Tarun Jha ◽  
Shovanlal Gayen

Camptothecin (CPT), obtained from Camptotheca acuminata (Nyssaceae), is a quinoline type of alkaloid. Apart from various traditional uses, it is mainly used as a potential cytotoxic agent acting against a variety of cancer cell lines. Though searches have been continued for last six decades, still it is a demanding task to design potent and cytotoxic CPTs. Different CPT analogs are synthesized to enhance the cytotoxic potential as well as to increase the pharmacokinetic properties of these analogs. Some of these analogs were proven to be clinically effective in different cancer cell lines. In this article, different CPT analogs have been highlighted extensively to get a detail insight about the structure-property relationships as well as different quantitative structure-activity relationships (QSARs) modeling of these analogs are also discussed. This study may be beneficial for designing newer CPT analogs in future.


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