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  2. Direct factor Xa inhibitors - Wikipedia

    en.wikipedia.org/wiki/Direct_factor_Xa_inhibitors

    A specialist may request a quantitative factor Xa assay in a situation of overdose. [2] Andexanet alfa, a specific antidote to reverse the anticoagulant activity of direct Xa inhibitors in the event of major bleeding, was approved by the FDA in 2018. [9] It is also available in the UK. [10]

  3. Low-molecular-weight heparin - Wikipedia

    en.wikipedia.org/wiki/Low-molecular-weight_heparin

    Results are given in units/mL of anti-factor Xa, such that high values indicate high levels of anticoagulation and low values indicate low levels of anticoagulation in the plasma sample. [ 17 ] LMWHs have a targeted therapeutic window of approximately 0.6–1.2 IU/ml. LMWH has a potency of 70 units/mg of anti-factor Xa activity and a ratio of ...

  4. Factor X - Wikipedia

    en.wikipedia.org/wiki/Factor_X

    The first crystal structure of human factor Xa was deposited in May 1993. To date, 191 crystal structures of factor Xa with various inhibitors have been deposited in the protein data bank. The active site of factor Xa is divided into four subpockets as S1, S2, S3 and S4. The S1 subpocket determines the major component of selectivity and binding.

  5. Tinzaparin sodium - Wikipedia

    en.wikipedia.org/wiki/Tinzaparin_sodium

    200 min. for Anti-Xa activity, 257. min for Anti-IIa activity [3] Identifiers; ... Anti-factor Xa levels can be measured, and are often used to monitor tinzaparin.

  6. Enoxaparin sodium - Wikipedia

    en.wikipedia.org/wiki/Enoxaparin_sodium

    Distribution: Volume of distribution (anti-Factor Xa activity) = 4.3 liters [17] Metabolism: Enoxaparin is metabolized in the liver into low molecular weight species by either or both desulfation and depolymerization. [17] Elimination: A single dose of a subcutaneous injection of enoxaparin has an elimination half-life of 4.5 hours. [17]

  7. Antithrombin - Wikipedia

    en.wikipedia.org/wiki/Antithrombin

    Antithrombin inactivates its physiological target enzymes, Thrombin, Factor Xa and Factor IXa with rate constants of 7–11 x 10 3, 2.5 x 10 3 M −1 s −1 and 1 x 10 M −1 s −1 respectively. [5] [24] The rate of antithrombin-thrombin inactivation increases to 1.5 - 4 x 10 7 M −1 s −1 in the presence of heparin, i.e. the reaction is ...

  8. Discovery and development of direct Xa inhibitors - Wikipedia

    en.wikipedia.org/wiki/Discovery_and_development...

    Factor Xa was identified as a promising target for the development of new anticoagulants in the early 1980s. In 1987 the first factor Xa inhibitor, the naturally occurring compound antistasin, was isolated from the salivary glands of the Mexican leech Haementeria officinalis. Antistasin is a polypeptide and a potent Xa inhibitor.

  9. Heparin - Wikipedia

    en.wikipedia.org/wiki/Heparin

    Fondaparinux targets anti-factor Xa activity rather than inhibiting thrombin activity, to facilitate a more subtle regulation of coagulation and an improved therapeutic index. It is a synthetic pentasaccharide, whose chemical structure is almost identical to the AT binding pentasaccharide sequence that can be found within polymeric heparin and ...