ChemicalBook--->CAS DataBase List--->120993-53-5

120993-53-5

120993-53-5 Structure

120993-53-5 Structure
IdentificationBack Directory
[Name]

Desirudin
[CAS]

120993-53-5
[Synonyms]

K-HIR02
Desirudin
[Molecular Formula]

C287H440N80O110S6
[MOL File]

120993-53-5.mol
[Molecular Weight]

6963.42
Hazard InformationBack Directory
[Uses]

Anticoagulant.
[Clinical Use]

Prophylaxis of DVT in patients undergoing orthopaedic surgery
[in vivo]

Desirudin (CGP 39393, 0.75-3.0 mg/kg, a bolus plus infusion administration, dogs model of cardiopulmonary bypass) is effective in Inhibiting clot formation[1]. Desirudin (0.01-1 mg/kg, Intravenous injections and subcutaneous injection, rat shunt model) inhibits thrombus development with ED50 values of 0.3 mg/kg (i.v.) and 1.0 mg/kg (s.c.), and inhibits venous stasis thrombosis with ED50 values of 0.01 mg/kg (i.v.) and 0.45 mg/kg (s.c.)[2].

Animal Model:Male mongrel dogs model of cardiopulmonary bypass[1]
Dosage:1.0 mg/kg + 0.75 mg/kg/h, 1.0 mg/kg + 1.50 mg/kg/h, 1.0 mg/kg + 2.25 mg/kg/h, 1.0 mg/kg + 3.0 mg/kg/h.
Administration:Administered as a bolus plus infusion
Result:Inhibited clot formation with no adverse hemodynamic or hematologic effects.
Animal Model:Rat shunt model of thrombus formation on a cotton-thread[2]
Dosage:0.01-1 mg/kg approximately
Administration:Intravenous injections, subcutaneous injection
Result:Inhibited thrombus development with ED50 values of 0.3 mg/kg (i.v.) and 1.0 mg/kg (s.c.). Inhibited venous stasis thrombosis with ED50 values of 0.01 mg/kg (i.v.) and 0.45 mg/kg (s.c.).
[Drug interactions]

Potentially hazardous interactions with other drugs
Anticoagulants, antiplatelets, fondaparinux, NSAIDs, heparin and dextran - increased risk of bleeding
[Metabolism]

Desirudin is metabolised and excreted by the kidney, and 40-50% of a dose is excreted unchanged in the urine
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