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Fondaparinux

CAS No.
816468-88-9
Chemical Name:
Fondaparinux
Synonyms
Sr 90107;Fondaparinux;Unii-J177fow5jl;Natural heparin pentasaccharide;alpha-D-Glucopyranoside, methyl o-2-deoxy-6-o-sulfo-2-(sulfoamino)-alpha-D-glucopyranosyl-(1-4)-o-beta-D-glucopyranuronosyl-(1-4)-o-2-deoxy-3,6-di-o-sulfo-2-(sulfoamino)-alpha-D-glucopyranosyl-(1-4)-o-2-o-sulfo-alpha-L-idopyranuronosyl-(1-4)-2-deoxy-2-(sulfoamino)-, 6-(hydrogen sulfate)
CBNumber:
CB6975195
Molecular Formula:
C31H53N3O49S8
Molecular Weight:
1508.26322
MDL Number:
MFCD00941363
MOL File:
816468-88-9.mol

Fondaparinux Properties

FDA UNII J177FOW5JL
ATC code B01AX05

Fondaparinux Chemical Properties,Uses,Production

Mechanism of action

The development of fondaparinux, a synthetically derived pentasaccharide that binds specifically to and activates antithrombin III, is a further refinement on the mechanism of action of heparin. Fondaparinus and a related analogue, idraparinux, are specific, indirect inhibitors of activated factor Xa via their activation of antithrombin. Fondaparinux has strategically located sulfonates that bind to antithrombin. Fondaparinux is structurally related to the antithrombotic binding site of heparin. Unlike heparin or LMWHs, however, these inhibitors have no effect on thrombin, because they lack the longer saccharide chains required for binding to thrombin. The highly sulfated heparins exhibit nonselective binding to a number of additional proteins, resulting in decreased bioavailability and significant variation in activity.

Pharmacokinetics

Fondaparinux is administered via subcutaneous injection with a single daily dose and shows complete absorption. The drug is highly bound to antithrombin III (~94%), with no significant binding to other plasma proteins. Because of the predictable anticoagulant effect, the drug does not require routine coagulation monitoring. The drug is not metabolized and is excreted in the urine unchanged within 72 hours in patients with normal renal function. Fondaparinux has an elimination half-life of 17 hours. Presently, no clinically significant drug interactions have been reported.

Clinical Use

Fondaparinux is the first selective factor Xa inhibitor that is approved for the prophylaxis of DVT, which may occur in patients undergoing hip fracture surgery or hip or knee replacement surgery (59).

Side effects

The most common side effect is major and minor bleeding, and the patient must be carefully monitored. The drug is not to be used when spinal anesthesia or spinal puncture is employed because of the potential for developing a blood clot in the spine. Fondaparinux has not been reported to cause thrombocytopenia, a condition seen with heparin. It is 100% bioavailable, with little or no protein binding.

Fondaparinux Preparation Products And Raw materials

Raw materials

Preparation Products

Fondaparinux Suppliers

Global( 4)Suppliers
Supplier Tel Email Country ProdList Advantage
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12338 58
alpha-D-Glucopyranoside, methyl o-2-deoxy-6-o-sulfo-2-(sulfoamino)-alpha-D-glucopyranosyl-(1-4)-o-beta-D-glucopyranuronosyl-(1-4)-o-2-deoxy-3,6-di-o-sulfo-2-(sulfoamino)-alpha-D-glucopyranosyl-(1-4)-o-2-o-sulfo-alpha-L-idopyranuronosyl-(1-4)-2-deoxy-2-(sulfoamino)-, 6-(hydrogen sulfate) Natural heparin pentasaccharide Sr 90107 Unii-J177fow5jl Fondaparinux 816468-88-9