Recent Advances in B-RAF Inhibitors as Anticancer Agents

2022 ◽  
pp. 105597
Author(s):  
Pathan Shahebaaz Khan ◽  
Patil Rajesh ◽  
Patil Rajendra ◽  
Manohar G. Chaskar ◽  
Arote Rohidas ◽  
...  
2018 ◽  
Vol 18 (15) ◽  
pp. 1265-1269 ◽  
Author(s):  
Sreekanth Thota ◽  
Daniel Alencar Rodrigues ◽  
Eliezer J. Barreiro

2012 ◽  
Vol 13 (11) ◽  
pp. 1432-1444 ◽  
Author(s):  
Yang Liu ◽  
Yijing Li ◽  
Shenghui Yu ◽  
Guisen Zhao

Yakhak Hoeji ◽  
2021 ◽  
Vol 65 (5) ◽  
pp. 344-348
Author(s):  
Gyubi Kim ◽  
Hansol Joo ◽  
Jong-Wha Jung

ChemInform ◽  
2005 ◽  
Vol 36 (51) ◽  
Author(s):  
R. Geney ◽  
J. Chen ◽  
I. Ojima

Author(s):  
Dharambir Kashyap ◽  
Hardeep Singh Tuli ◽  
Mukerrem Betul Yerer ◽  
Anil K. Sharma ◽  
Harpal Singh Buttar ◽  
...  

Folia Medica ◽  
2021 ◽  
Vol 63 (1) ◽  
pp. 7-14
Author(s):  
Ishan Panchal ◽  
Archana Navale ◽  
Ashish Shah ◽  
Sandip Badeliya ◽  
Rati Tripathi

Cancer refers to the group of diseases characterized by uncontrolled growth of abnormal cells. It spreads throughout the body which makes this disease one of the huge global threats to mankind. Intensive research over the years has established deregulation of mam-malian target of rapamycin pathway in cancer. This has led to the development of mammalian target of rapamycin inhibitors. Several inhibitors of the mammalian target of rapamycin are under preclinical and early clinical trials. Researchers have investigated a series of furoquinoline, phenyl sulphonylureas, 4-acrylamido-quinoline, pyrazolochalcones, imidazole [4,5-b] pyridine, thienopyrimidine, aminopyrimidin scaffolds in the last three years. This review provides comprehensive information and critical discussions on designing of novel selective inhibitors of mammalian target of rapamycin with superior activity in the treatment of cancer. 


2022 ◽  
Vol 25 ◽  
pp. 24-40
Author(s):  
Emilio Mateev ◽  
Maya Georgieva ◽  
Alexander Zlatkov

With the significant increase of patients suffering from different types of cancer, it is evident that prompt measures in the development of novel and effective agents need to be taken. Pyrrole moiety has been found in various active compounds with anti-inflammatory, antiseptic, antibacterial, lipid-lowering and anticancer properties. Recent advances in the exploration of highly active and selective cytotoxic structures containing pyrrole motifs have shown promising data for future investigations. Accordingly, this review presents an overview of recent developments in the pyrrole derivatives as anticancer agents, with a main focus towards the key moieties required for the anti-tumor activities. Pyrrole molecules comprising prominent targeting capacities against microtubule polymerization, tyrosine kinases, cytochrome p450 family 1, histone deacetylase and bcl-2 proteins were reported. In addition, several mechanisms of action, such as apoptosis, cell cycle arrest, inhibiting kinases, angiogenesis, disruption of cell migration, modulation of nuclear receptor responsiveness and others were analyzed. Furthermore, in most of the discussed cases we provided synthesis schemes of the mentioned molecules. Overall, the utilization of pyrrole scaffold for the design and synthesis of novel anticancer drugs could be a promising approach for future investigations.  


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