| Literature DB >> 21164526 |
Elisabeth Perzborn1, Susanne Roehrig, Alexander Straub, Dagmar Kubitza, Frank Misselwitz.
Abstract
The activated serine protease factor Xa is a promising target for new anticoagulants. After studies on naturally occurring factor Xa inhibitors indicated that such agents could be effective and safe, research focused on small-molecule direct inhibitors of factor Xa that might address the major clinical need for improved oral anticoagulants. In 2008, rivaroxaban (Xarelto; Bayer HealthCare) became the first such compound to be approved for clinical use. This article presents the history of rivaroxaban's development, from the structure-activity relationship studies that led to its discovery to the preclinical and clinical studies, and also provides a brief overview of other oral anticoagulants in advanced clinical development.Entities:
Mesh:
Substances:
Year: 2010 PMID: 21164526 DOI: 10.1038/nrd3185
Source DB: PubMed Journal: Nat Rev Drug Discov ISSN: 1474-1776 Impact factor: 84.694