Substance

ID:290

Names and Identifiers
IUPAC name
3-[(5-{[6-carboxy-4,5-dihydroxy-3-(sulfooxy)oxan-2-yl]oxy}-6-(hydroxymethyl)-3-(sulfoamino)-4-(sulfooxy)oxan-2-yl)oxy]-6-({5-acetamido-4,6-dihydroxy-2-[(sulfooxy)methyl]oxan-3-yl}oxy)-4-hydroxy-5-(sulfooxy)oxane-2-carboxylic acid
IUPAC Traditional name
heparin
Synonyms
Ardeparin
Brand Name
Normiflo
Registration numbers
PubChem CID
PubChem SID
Properties
Physical Property
Solubility
Soluble
Molecule Details
Drug Groups
approved; withdrawn
Description
Ardeparin, marketed under the US trade name Normiflo, is a low molecular weight heparin (LMWH) anticoagulant used for the prevention of postoperative venous thrombosis. Ardeparin is derived via peroxide degradation of heparin extracted from porcine intestinal mucosa. Its molecular weight ranges from 2000 to 15,000 with an average molecular weight of 5500 to 6500. Normiflo was withdrawn from the US market in March 2000.
Indication
For prevention of deep vein thrombosis, which may result in pulmonary embolism, following knee surgery.
Pharmacology
Ardeparin, an anticoagulant, is a fractionated heparin. It acts at multiple sites in the normal coagulation system to inhibit reactions that lead to the clotting of blood and the formation of fibrin clots both in vitro and in vivo.
Toxicity
Symptoms of overdose may include excessive bleeding and bruising.
Affected Organisms
Humans and other mammals
Biotransformation
Liver and the reticulo-endothelial system are the sites of biotransformation.
Absorption
Well absorbed following subcutaneous administration, with a mean bioavailability of 92% (based on anti-factor Xa activity).
Half Life
Elimination half-life for anti-factor Xa activity averages 3.3 hours following a single intravenous dose, while elimination half-life for anti-factor IIa activity averages 1.2 hours following a single intravenous dose.
External Links
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data