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Imiglucerase: profile and news
Genzyme Reports Financial Results for Fourth Quarter of 2005 and ... Feb 15, 2006 Genzyme Reports Financial Results for Fourth Quarter of 2005 and ... Feb 15, 2006 Other information Indication For treatment of Gaucher's disease (deficiency in glucocerebrosidase) Pharmacology Gaucher disease is characterized by a functional deficiency in Beta-glucocerebrosidase enzymatic activity and the resultant accumulation of lipid glucocerebroside in tissue macrophages which become engorged and are termed Gaucher cells. Gaucher cells are typically found in liver, spleen and bone marrow. This can lead to an enlarged spleen and liver (hepatosplenomegaly). Secondary hematologic sequelae include severe anemia and thrombocytopenia. Injections of alglucerase into Gaucher disease patients leads to elevated serum levels of the enzyme and reduction in the accumulation of glucocerebroside Mechanism Of Action Alglucerase catalyzes the hydrolysis of the glycolipid, glucocerebroside, to glucose and ceramide as part of the normal degradation pathway for membrane lipids. Drug Category Enzyme replacement Brand Names/Synonyms Glucosylceramidase precursor;Beta-glucocerebrosidase;Acid beta-glucosidase;D-glucosyl-N-acylsphingosine glucohydrolase;Alglucerase;Imiglucerase; Ceredase (Genzyme Corp) Dosage Forms Not Available Absorption Not Available Interactions Not Available Chemical IUPAC Name Human Beta-glucocerbrosidase Chemical Formula C2532H3854N672O711S16 Half Life 3.6-10.4 min Drug Type Approved Drug # Accession No BIOD00037 CAS Registry Number 37228-64-1; 143003-46-7 |
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