Advances in the Development of Novel Factor Xa Inhibitors: A Patent Review
- PMID: 29692238
- DOI: 10.2174/1389557518666180424120726
Advances in the Development of Novel Factor Xa Inhibitors: A Patent Review
Abstract
Development of new anticoagulants has been in constant demand throughout the world due to increasing rate of morbidity and mortality caused by thrombotic diseases. Factor Xa (FXa), one of the enzymes and validated target for anticoagulation, regulates the production of thrombin in the coagulation cascade. The importance of oral FXa inhibitors like rivaroxaban, apixaban and edoxaban in thromboembolic conditions is well supported by increasing number of patents and research publications during the recent years. Direct FXa inhibitors as antithrombotic agents offer selective, efficacious and orally active therapy with respect to the other traditional anticoagulants. Newly developed patented molecules are mainly structural bioisosteres of existing drugs and have exhibited better efficacy and safety profile. Development of antidotes for oral direct FXa inhibitors is in pipeline and their expected approval for therapeutic purposes will be further beneficial to anticoagulation therapy. This review is mainly focused on industrial and academic patents on the discovery of direct FXa inhibitors. The review covers patented compounds from December 2011 till date, describing various structural modifications along with biological activity data and advances in the process and formulation technologies of the reported FXa inhibitors.
Keywords: Anticoagulant; VTE; apixaban; factor Xa inhibitor; rivaroxaban; thrombosis..
Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.
Similar articles
-
Novel Anthranilamide-Based FXa Inhibitors: Drug Design, Synthesis and Biological Evaluation.Molecules. 2016 Apr 14;21(4):491. doi: 10.3390/molecules21040491. Molecules. 2016. PMID: 27089317 Free PMC article.
-
Synthesis and evaluation of anthranilamide-based derivatives as FXa inhibitors.Oncotarget. 2017 Jun 6;8(23):37186-37199. doi: 10.18632/oncotarget.16427. Oncotarget. 2017. PMID: 28415603 Free PMC article.
-
Nonhemostatic Activities of Factor Xa: Are There Pleiotropic Effects of Anti-FXa Direct Oral Anticoagulants?Angiology. 2019 Nov;70(10):896-907. doi: 10.1177/0003319719840861. Epub 2019 Apr 22. Angiology. 2019. PMID: 31010298 Review.
-
The emergence of factor Xa inhibitors for the treatment of cardiovascular diseases: a patent review.Expert Opin Ther Pat. 2012 Jun;22(6):645-61. doi: 10.1517/13543776.2012.680438. Epub 2012 Jun 3. Expert Opin Ther Pat. 2012. PMID: 22655676 Review.
-
Design, synthesis and biological evaluation of novel 2,3-dihydroquinazolin- 4(1H)-one derivatives as potential fXa inhibitors.Eur J Med Chem. 2017 Jan 5;125:411-422. doi: 10.1016/j.ejmech.2016.09.055. Epub 2016 Sep 19. Eur J Med Chem. 2017. PMID: 27689724
Cited by
-
Techniques for Detection of Clinical Used Heparins.Int J Anal Chem. 2021 May 6;2021:5543460. doi: 10.1155/2021/5543460. eCollection 2021. Int J Anal Chem. 2021. PMID: 34040644 Free PMC article. Review.
-
Assessing the Role of a Malonamide Linker in the Design of Potent Dual Inhibitors of Factor Xa and Cholinesterases.Molecules. 2022 Jul 2;27(13):4269. doi: 10.3390/molecules27134269. Molecules. 2022. PMID: 35807514 Free PMC article.
-
Innovative Three-Step Microwave-Promoted Synthesis of N-Propargyltetrahydroquinoline and 1,2,3-Triazole Derivatives as a Potential Factor Xa (FXa) Inhibitors: Drug Design, Synthesis, and Biological Evaluation.Molecules. 2020 Jan 23;25(3):491. doi: 10.3390/molecules25030491. Molecules. 2020. PMID: 31979319 Free PMC article.
-
Inhibition of dimeric SARS-CoV-2 Mpro displays positive cooperativity and a mixture of covalent and non-covalent binding.iScience. 2025 May 28;28(7):112773. doi: 10.1016/j.isci.2025.112773. eCollection 2025 Jul 18. iScience. 2025. PMID: 40655098 Free PMC article.
-
Discovery and development of Factor Xa inhibitors (2015-2022).Front Pharmacol. 2023 Feb 21;14:1105880. doi: 10.3389/fphar.2023.1105880. eCollection 2023. Front Pharmacol. 2023. PMID: 36909153 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources