Entry 1 |
(1) Primary information |
---|
ID | 1142 |
ThPP ID | Th1020 |
Therapeutic Peptide/Protein Name | Asparaginase |
Sequence | Elspar Sequence: QMSLQQELRYIEALSAIVETGQKMLEAGESALD view full sequnce in fasta |
Functional Classification | Ic |
Molecular Weight | 31731.9 |
Chemical Formula | C1377H2208N382O442S17 |
Isoelectric Point | 4.67 |
Hydrophobicity | 0.059 |
Melting Point (℃) | N.A. |
Half Life | 8-30 hours |
Description | L-asparagine amidohydrolase from E. coli |
Indication/Disease | To treat acute lympocytic leukemia and non-Hodgkins lymphoma |
Pharmacodynamics | In most patients with acute leukemia, the malignant cells are dependent on an exogenous source of asparagine for survival. Normal cells, however, are able to synthesize asparagine and thus are affected less by the rapid depletion produced by treatment with the enzyme asparaginase. Elspar exploits a metabolic defect in asparagine synthesis of some malignant cells. |
Mechanism of Action | Asparaginase converts asparagine to aspartic acid and ammonia. It facilitates production of oxalo-acetate which is needed for general cellular metabolism. Some malignant cells lose the ability to produce asparagine and thus the loss of exogenous sources of asparagine leads to cell death. |
Toxicity | N.A. |
Metabolism | N.A. |
Absorption | N.A. |
Volume of Distribution | N.A. |
Clearance | N.A. |
Categories | Antineoplastic Agents |
Patents Number | N.A. |
Date of Issue | N.A. |
Date of Expiry | N.A. |
Drug Interaction | Trastuzumab may increase the risk of neutropenia and anemia. Monitor closely for signs and symptoms of adverse events. |
Target | L-asparagine |
Information of corresponding available drug in the market |
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Brand Name | Elspar |
Company | Merck & Co. Inc |
Brand Discription | Elspar contains the enzyme L-asparagine amidohydrolase, type EC-2, derived from Escherichia coli. Elspar activity is expressed in terms of International Units according to the recommendation of the International Union of Biochemistry. One International Un |
Prescribed for | To treat acute lymphocytic leukemia. It is used along with other cancer medicines. Elspar is an antineoplastic agent that works by decreasing the amount of asparagine in the body, which kills certain leukemia cells |
Chemical Name | N.A. |
Formulation | Each vial contains 10,000 International Units of asparaginase and 80 mg of mannitol. |
Physcial Appearance | Lyophilized plug or powder |
Route of Administration | Intravenous or intramuSubcutaneousular. Intravenou |
Recommended Dosage | The recommended dose of Elspar is 6,000 International Units/m_ intramuscularly (IM) or intravenously (IV) three times a week. |
Contraindication | Allergic |
Side Effects | Fever, chills (see flu like symptoms), Nausea and vomiting, Allergic reaction, (sudden onset of wheezing, itching, rash, face swelling, agitation, low blood pressure). You will be monitored closely for this reaction, Poor appetite, Stomach cramping |
Useful Link | http://www.rxlist.com/elspar-drug.htm |
PubMed ID | 17554375, 14499708, 25098829, 24436152, 23794007, 22499236, 20824725 |
3-D Structure | Th1020 (View) or (Download) |
Entry 2 |
(2) Primary information |
---|
ID | 1143 |
ThPP ID | Th1020 |
Therapeutic Peptide/Protein Name | Asparaginase |
Sequence | Elspar Sequence: QMSLQQELRYIEALSAIVETGQKMLEAGESALD view full sequnce in fasta |
Functional Classification | Ic |
Molecular Weight | 31731.9 |
Chemical Formula | C1377H2208N382O442S17 |
Isoelectric Point | 4.67 |
Hydrophobicity | 0.059 |
Melting Point (℃) | N.A. |
Half Life | 8-30 hours |
Description | L-asparagine amidohydrolase from E. coli |
Indication/Disease | To treat acute lympocytic leukemia and non-Hodgkins lymphoma |
Pharmacodynamics | In most patients with acute leukemia, the malignant cells are dependent on an exogenous source of asparagine for survival. Normal cells, however, are able to synthesize asparagine and thus are affected less by the rapid depletion produced by treatment with the enzyme asparaginase. Elspar exploits a metabolic defect in asparagine synthesis of some malignant cells. |
Mechanism of Action | Asparaginase converts asparagine to aspartic acid and ammonia. It facilitates production of oxalo-acetate which is needed for general cellular metabolism. Some malignant cells lose the ability to produce asparagine and thus the loss of exogenous sources of asparagine leads to cell death. |
Toxicity | N.A. |
Metabolism | N.A. |
Absorption | N.A. |
Volume of Distribution | N.A. |
Clearance | N.A. |
Categories | Antineoplastic Agents |
Patents Number | N.A. |
Date of Issue | N.A. |
Date of Expiry | N.A. |
Drug Interaction | N.A. |
Target | N.A. |
Information of corresponding available drug in the market |
---|
Brand Name | N.A. |
Company | N.A. |
Brand Discription | N.A. |
Prescribed for | N.A. |
Chemical Name | N.A. |
Formulation | N.A. |
Physcial Appearance | N.A. |
Route of Administration | N.A. |
Recommended Dosage | N.A. |
Contraindication | N.A. |
Side Effects | Mouth sores, Pancreatitis (inflammation of the pancreas) in up to 10% of patients. Mainly noted in blood tests that return to normal after therapy is discontinued. Rarely may be severe causing symptoms. Symptoms of acute pancreatitis include: (pain in the upper abdomen that worsens with eating, swollen and tender abdomen, nausea, vomiting, fever, and rapid pulse). |
Useful Link | http://www.rxlist.com/elspar-drug/indications-dosage.htm |
PubMed ID | 17554375, 14499708, 25098829, 24436152, 23794007, 22499236, 20824725 |
3-D Structure | Th1020 (View) or (Download) |
Entry 3 |
(3) Primary information |
---|
ID | 1144 |
ThPP ID | Th1020 |
Therapeutic Peptide/Protein Name | Asparaginase |
Sequence | Elspar Sequence: QMSLQQELRYIEALSAIVETGQKMLEAGESALD view full sequnce in fasta |
Functional Classification | Ic |
Molecular Weight | 31731.9 |
Chemical Formula | C1377H2208N382O442S17 |
Isoelectric Point | 4.67 |
Hydrophobicity | 0.059 |
Melting Point (℃) | N.A. |
Half Life | 8-30 hours |
Description | L-asparagine amidohydrolase from E. coli |
Indication/Disease | To treat acute lympocytic leukemia and non-Hodgkins lymphoma |
Pharmacodynamics | In most patients with acute leukemia, the malignant cells are dependent on an exogenous source of asparagine for survival. Normal cells, however, are able to synthesize asparagine and thus are affected less by the rapid depletion produced by treatment with the enzyme asparaginase. Elspar exploits a metabolic defect in asparagine synthesis of some malignant cells. |
Mechanism of Action | Asparaginase converts asparagine to aspartic acid and ammonia. It facilitates production of oxalo-acetate which is needed for general cellular metabolism. Some malignant cells lose the ability to produce asparagine and thus the loss of exogenous sources of asparagine leads to cell death. |
Toxicity | N.A. |
Metabolism | N.A. |
Absorption | N.A. |
Volume of Distribution | N.A. |
Clearance | N.A. |
Categories | Antineoplastic Agents |
Patents Number | N.A. |
Date of Issue | N.A. |
Date of Expiry | N.A. |
Drug Interaction | N.A. |
Target | N.A. |
Information of corresponding available drug in the market |
---|
Brand Name | N.A. |
Company | N.A. |
Brand Discription | N.A. |
Prescribed for | N.A. |
Chemical Name | N.A. |
Formulation | N.A. |
Physcial Appearance | N.A. |
Route of Administration | N.A. |
Recommended Dosage | N.A. |
Contraindication | N.A. |
Side Effects | Central neurotoxicity: excessive sleepiness, depression, hallucinations, agitation, disorientation or seizure, stupor, confusion and/or coma. |
Useful Link | http://www.drugs.com/cdi/elspar.html |
PubMed ID | 17554375, 14499708, 25098829, 24436152, 23794007, 22499236, 20824725 |
3-D Structure | Th1020 (View) or (Download) |