出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/10/15 17:02:03」(JST)
Systematic (IUPAC) name | |
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N-isopropyl-4-[(2-methylhydrazino)methyl]benzamide | |
Clinical data | |
Trade names | Matulane |
AHFS/Drugs.com | monograph |
MedlinePlus | a682094 |
Pregnancy cat. | D (AU) D (US) |
Legal status | ℞ Prescription only |
Routes | Oral (Gel Capsule), intravenous |
Pharmacokinetic data | |
Bioavailability | ? |
Metabolism | Hepatic, Renal |
Half-life | 10 minutes |
Excretion | Renal |
Identifiers | |
CAS number | 671-16-9 Y |
ATC code | L01XB01 |
PubChem | CID 4915 |
DrugBank | DB01168 |
ChemSpider | 4746 Y |
UNII | 35S93Y190K Y |
KEGG | D08423 Y |
ChEBI | CHEBI:71417 N |
ChEMBL | CHEMBL1321 Y |
Chemical data | |
Formula | C12H19N3O |
Mol. mass | 221.299 g/mol |
SMILES
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InChI
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Procarbazine (Matulane (US), Natulan (Canada), Indicarb (India) is an antineoplastic chemotherapy drug for the treatment of Hodgkin's lymphoma and certain brain cancers (such as Glioblastoma multiforme). It is a member of a group of medicines called alkylating agents. It gained FDA Approved in July 1969. The drug is metabolized and activated in the liver. It also inhibits MAO thus increasing the effects of sympathomimetics, TCAs, and tyramine.
Its mechanism of action is not fully understood. Metabolism yields azo-procarbazine and hydrogen peroxide[citation needed] which results in the breaking of DNA strands.
When used to treat Hodgkin's Lymphoma (HL), it is often delivered as part of the BEACOPP regimen that includes Bleomycin, Etoposide, Adriamycin, Cyclophosphamide, Vincristine (tradename Oncovin), Prednisone, and Procarbazine. The first combination chemotherapy developed for Hodgkin's Lymphoma, MOPP also included Procarbazine (ABVD has supplanted MOPP as standard first line treatment for HL, with BEACOPP as an alternative for advanced/unfavorable HL). Alternatively, when used to treat certain brain tumors (malignant gliomas), it is often dosed as PCV when combined with Lomustine (often called CCNU) and Vincristine.
When combined with ethanol, procarbazine may cause a disulfiram-like reaction in some patients. It also inhibits the liver's CYP450 microsomal system, which leads to an increased effect of barbiturates, phenothiazenes, and narcotics normally metabolized by the CYP450 enzymes. Has monamine oxidase inhibition properties (MAOI), and should not be taken with most antidepressants and certain migraine medications.
Inhibits MAO in the gastrointestinal system thus can cause hypertensive crises if associated with the ingestion of tyramine-rich foods such as aged cheeses.
Procarbazine rarely causes chemotherapy-induced peripheral neuropathy,[1] a progressive, enduring, often irreversible tingling numbness, intense pain, and hypersensitivity to cold, beginning in the hands and feet and sometimes involving the arms and legs.[2]
Adult: as part of the BEACOPP chemotherapy regimen: 100 mg/m²/day given for 7 days. Dose should be adjusted for renal (kidney) disease or hepatic (liver) disease.
50 mg capsules.
This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (August 2010) |
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リンク元 | 「プロカルバジン」 |
拡張検索 | 「procarbazine hydrochloride」 |
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