Outline of gelatinase inhibitors as anti-cancer agents: A patent mini-review for 2010-present
European Journal of Medicinal Chemistry, ISSN: 0223-5234, Vol: 213, Page: 113044
2021
- 26Citations
- 23Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations26
- Citation Indexes26
- 26
- CrossRef9
- Captures23
- Readers23
- 23
Review Description
Matrix metalloproteinases (MMPs) are involved in several pathological and physiological functions. Gelatinases (MMP-2 and -9) have significant attention as therapeutic targets against cancer. Gelatinase inhibitors have demonstrated their effectiveness in several diseases including cancer. However, it is quite a challenging task to develop inhibitors as a therapeutic agent. This review summarizes the patent dedicated to the medicinal chemistry of gelatinase inhibitor reported over last decades. We examine the patent being pursued for gelatinase inhibitor development to highlight the key issues. The main aim is to provide the scientific community with an overview of the patented gelatinase inhibitors to allow further development. During early 2000s, some MMP inhibitors failed to pass the clinical trials. Hence, the lessons learned from early evidence and recent knowledge in that field will rejuvenate the development of selective inhibitors. Various studies and patents have continued in the recent years to expand knowledge. Continuously, our research team has been involved in the design of potent and selective gelatinase inhibitors for the past few years. This study is a part of our efforts. This study may be beneficial in the design and development of better gelatinase inhibitors in the future.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0223523420310163; http://dx.doi.org/10.1016/j.ejmech.2020.113044; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85097088284&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/33279289; https://linkinghub.elsevier.com/retrieve/pii/S0223523420310163; https://dx.doi.org/10.1016/j.ejmech.2020.113044
Elsevier BV
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