Detailed description page of ThPDB2

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10308 details
Primary information
ID10308
Therapeutic IDTh1043
Protein NameRasburicase
Sequence>Th1043_Rasburicase SAVKAARYGKDNVRVYKVHKDEKTGVQTVYEMTVCVLLEGEIETSYTKADNSVIVATDSIKNTIYITAKQNPVTPPELFGSILGTHFIEKYNHIHAAHVNIVCHRWTRMDIDGKPHPHSFIRDSEEKRNVQVDVVEGKGIDIKSSLSGLTVLKSTNSQFWGFLRDEYTTLKETWDRILSTDVDATWQWKNFSGLQEVRSHVPKFDATWATAREVTLKTFAEDNSASVQATMYKMAEQILARQQLIETVEYSLPNKHYFEIDLSWHKGLQNTGKNAEVFAPQSDPNGLIKCTVGRSSLKSKL
Molecular Weight34109.5
Chemical FormulaC1521H2381N417O461S7
Isoelectric Point7.16
Hydrophobicity-0.465
Melting pointNA
Half-life18 hours
DescriptionRasburicase is a recombinant urate-oxidase enzyme produced by a genetically modified Saccharomyces cerevisiae< strain. The cDNA coding for rasburicase was cloned from a strain of Aspergillus flavus.
Indication/DiseaseFor treatment of hyperuricemia, reduces elevated plasma uric acid levels (from chemotherapy).
PharmacodynamicsDrugs used to treat lympohoid leukemia, non-Hodgkin's lymphoma and acute myelogenous leukemia often lead to the accumulation of toxic plasma levels of purine metabolites (i.e. uric acid). The injection of rasburicase reduces levels of uric acid and mitigates the toxic effects of chemotherapy induced tumor lysis.
Mechanism of ActionRasburicase catalyzes enzymatic oxidation of uric acid into an inactive and soluble metabolite (allantoin).
ToxicityNA
MetabolismNA
AbsorptionNA
NA
ClearanceNA
CategoriesAntigout Preparations, Detoxifying Agents for Antineoplastic Treatment, Enzymes, Enzymes and Coenzymes, Methemoglobinemia Associated Agents, Musculo-Skeletal System, Oxidoreductases, Recombinant Proteins, Uric Acid-specific Enzyme
Patents NumberNA
Date of IssueNA
Date of ExpiryNA
Drug InteractionCyanide Antidote Kit (amyl nitrite / sodium nitrite / sodium thiosulfate)
TargetNA
Brand NameFasturtec
CompanySanofi Aventis
Brand DescriptionSanofi Aventis
Prescribed ForFasturtec is used to treat and prevent high levels of uric acid in the blood in order to prevent kidney failure. It is used in adults and children with blood cancers who are at risk of a sudden rise in uric acid levels when they start to receive chemother
Chemical NameNA
FormulationNA
Physical Appearance Powder and solvent that are made upto make solution.
Route of AdministrationIntravenous administartion
Recommended DosageThe recommended dose is 0.2 mg per kilogram body weight in both children and adults, given as a daily infusion for up to seven days. The duration of treatment is adjusted depending on the patient’s blood levels of uric acid and the doctor’s judgment.
ContraindicationHypersensitivity
Side EffectsRash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; blue or gray skin color; chest pain; chills; coughing up blood; dark urine; fever; irregular heartbeat; numbness or tingling of the skin; persistent sore throat; severe dizziness; shortness of breath, trouble breathing, or wheezing; swelling of the hands or feet; weakness; yellowing of the eyes and skin.
Useful Link 1Link
Useful Link 2NA
RemarksNA