出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/07/25 16:18:36」(JST)
Systematic (IUPAC) name | |
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4-[bis(chloroethyl)amino]phenylalanine
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Clinical data | |
Trade names | Alkeran |
AHFS/Drugs.com | monograph |
MedlinePlus | a682220 |
Legal status |
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Routes of administration |
Oral, intravenous |
Pharmacokinetic data | |
Bioavailability | 25% to 89% |
Metabolism | hydrolysis |
Biological half-life | 1.5 ± 0.8 hours |
Excretion | Renal, significantly metabolised |
Identifiers | |
CAS Registry Number | 148-82-3 Y |
ATC code | L01AA03 |
PubChem | CID: 4053 |
IUPHAR/BPS | 7620 |
DrugBank | DB01042 Y |
ChemSpider | 405297 Y |
UNII | Q41OR9510P Y |
KEGG | D00369 Y |
ChEBI | CHEBI:28876 Y |
ChEMBL | CHEMBL852 Y |
Synonyms | 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]-propanoic acid |
Chemical data | |
Formula | C13H18Cl2N2O2 |
Molecular mass | 305.2 g/mol |
SMILES
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InChI
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Y (what is this?) (verify) |
Melphalan (trade name Alkeran, in former USSR also known as Sarcolysin) is a chemotherapy drug belonging to the class of nitrogen mustard alkylating agents.
An alkylating agent adds an alkyl group (CnH2n+1) to DNA. It attaches the alkyl group to the guanine base of DNA, at the number 7 nitrogen atom of the imidazole ring.
Otherwise known as L-Phenylalanine Mustard, or L-PAM, melphalan is a phenylalanine derivative of mechlorethamine.
Melphalan chemically alters through alkylation of the DNA nucleotide guanine, and causes linkages between strands of DNA. This chemical alteration inhibits DNA synthesis and RNA synthesis, functions necessary for cells to survive. These changes cause cytotoxicity in both dividing and non-dividing tumor cells.[1]
It is used to treat multiple myeloma,[2] ovarian cancer, AL amyloidosis, and occasionally malignant melanoma.
The agent was first investigated as a possible drug for use in melanoma. It was not found to be effective, but has been found to be effective in the treatment of myeloma.
Melphalan is currently being used to treat ocular retinoblastoma, a pediatric solid tumor. This is accomplished via transarterial catheter based slow pulsed infusion into the ophthalmic artery.[3]
Oral or intravenous; dosing varies by purpose and route of administration as well as patient weight.
Melphalan Prescribing Information: Alkeran[4]
Melphalan Patient Information: MedlinePlus[5]
Melphalan Material Safety Data Sheet (MSDS): Sequoia Research Products[6]
Common side effects include:
Less common side effects include:
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リンク元 | 「メルファラン」「L-フェニルアラニンマスタード」 |
関連記事 | 「PAM」「PA」「L」「P」 |
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