ChemicalBook--->CAS DataBase List--->143653-53-6

143653-53-6

143653-53-6 Structure

143653-53-6 Structure
IdentificationBack Directory
[Name]

abciximab
[CAS]

143653-53-6
[Synonyms]

Reopro
CentoRx
Rheopro
Unii-X85G7936gv
Immunoglobulin G1, (human-mouse monoclonal c7E3 clone p7E3VHhCgamma1 Fab fragment anti-human glycoprotein IIb/IIIa receptor), disulfide with human-mouse monoclonal c7E3 clone p7E3VkappahCkappa light chain
Chemical PropertiesBack Directory
[storage temp. ]

Store at -80°C
Safety DataBack Directory
[Hazardous Substances Data]

143653-53-6(Hazardous Substances Data)
Hazard InformationBack Directory
[Uses]

Monoclonal antibody (antithrombotic).
[Brand name]

ReoPro (Lilly).
[Clinical Use]

Antiplatelet agent:
Prevention of ischaemic cardiac complications in patients undergoing percutaneous coronary intervention
Short-term prevention of myocardial infarction in patients with unstable angina not responding to treatment or awaiting percutaneous coronary intervention.
[Enzyme inhibitor]

This antithrombotic (MW = 47455 g/mol; CAS 143653-53-6; also known as Reopro?) consists of an immunoglobulin G1 Fab fragment from a chimeric human-murine monoclonal antibody directed against the human platelet glycoprotein IIb/IIIa receptor. Abciximab also facilitates the dispersal of newly formed platelet aggregates in vitro, by partially displacing fibrinogen from activated GPIIb/IIIareceptors. In vivo, abciximab may destabilize coronary thrombi by preventing aggregate formation and dispersing mural thrombi. Target(s): coagulation factor Xa, in presence of heparin; glycoprotein IIb/IIIa receptor.
[Drug interactions]

Potentially hazardous interactions with other drugs
Heparin, anticoagulants, antiplatelets and thrombolytics: increased risk of bleeding.
[Metabolism]

Following IV administration, abciximab rapidly binds to the platelet GPIIb/IIIa receptors, and remains in the circulation for 15 days or more in a platelet-bound state. Metabolism is via proteolytic cleavage
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