Cyclooxygenase-2 (COX-2) as a Target of Anticancer Agents: A Review of Novel Synthesized Scaffolds Having Anticancer and COX-2 Inhibitory Potentialities

Cancer is a serious threat to human beings and is the second-largest cause of death all over the globe. Chemotherapy is one of the most common treatments for cancer; however, drug resistance and severe adverse effects are major problems associated with anticancer therapy. New compounds with multi-ta...

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Bibliographic Details
Main Authors: Noor ul Amin Mohsin (Author), Sana Aslam (Author), Matloob Ahmad (Author), Muhammad Irfan (Author), Sami A. Al-Hussain (Author), Magdi E. A. Zaki (Author)
Format: Book
Published: MDPI AG, 2022-11-01T00:00:00Z.
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LEADER 00000 am a22000003u 4500
001 doaj_25bce8b65f8e44bd82dd6f2c7741a1e3
042 |a dc 
100 1 0 |a Noor ul Amin Mohsin  |e author 
700 1 0 |a Sana Aslam  |e author 
700 1 0 |a Matloob Ahmad  |e author 
700 1 0 |a Muhammad Irfan  |e author 
700 1 0 |a Sami A. Al-Hussain  |e author 
700 1 0 |a Magdi E. A. Zaki  |e author 
245 0 0 |a Cyclooxygenase-2 (COX-2) as a Target of Anticancer Agents: A Review of Novel Synthesized Scaffolds Having Anticancer and COX-2 Inhibitory Potentialities 
260 |b MDPI AG,   |c 2022-11-01T00:00:00Z. 
500 |a 10.3390/ph15121471 
500 |a 1424-8247 
520 |a Cancer is a serious threat to human beings and is the second-largest cause of death all over the globe. Chemotherapy is one of the most common treatments for cancer; however, drug resistance and severe adverse effects are major problems associated with anticancer therapy. New compounds with multi-target inhibitory properties are targeted to surmount these challenges. Cyclooxygenase-2 (COX-2) is overexpressed in cancers of the pancreas, breast, colorectal, stomach, and lung carcinoma. Therefore, COX-2 is considered a significant target for the synthesis of new anticancer agents. This review discusses the biological activity of recently prepared dual anticancer and COX-2 inhibitory agents. The most important intermolecular interactions with the COX-2 enzyme have also been presented. Analysis of these agents in the active area of the COX-2 enzyme could guide the introduction of new lead compounds with extreme selectivity and minor side effects. 
546 |a EN 
690 |a drug design 
690 |a hybrid molecules 
690 |a cancer cell lines 
690 |a molecular docking 
690 |a COX-2 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 15, Iss 12, p 1471 (2022) 
787 0 |n https://www.mdpi.com/1424-8247/15/12/1471 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/25bce8b65f8e44bd82dd6f2c7741a1e3  |z Connect to this object online.