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Cyclophosphamide

Catalog No. DB00531 Name DrugBank
CAS Number 6055-19-2 Website http://www.ualberta.ca/
M. F. C7H15Cl2N2O2P Telephone (780) 492-3111
M. W. 261.085961 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 413

SYNONYMS

IUPAC name
2-[bis(2-chloroethyl)amino]-1,3,2$l^{5}-oxazaphosphinan-2-one
IUPAC Traditional name
cyclophosphamide
Brand Name
ASTA
Cyclophosphamid
Cytoxan Lyoph
Enduxan
Hexadrin
Endoxan R
Asta B 518
CPA
Claphene
Cyclophosphamidum
Cyclophosphan
Cyclophosphoramide
Cyklofosfamid
Endoxana
Lyophilized Cytoxan
Neosar
Zyklophosphamid
CP
CTX
CY
Clafen
Cyclophosphamide Monohydrate
Cyclophosphamide Sterile
Cyclophosphane
Cyclostin
Cytophosphan
Cytoxan
Endoxan
Endoxan-Asta
Endoxanal
Genoxal
Mitoxan
Procytox
Rcra Waste Number U058
Semdoxan
Sendoxan
Senduxan
Revimmune
Endoxane
Synonyms
cyclophosphamide

DATABASE IDS

PubChem CID 2907
CAS Number 6055-19-2
PubChem SID 46505441

PROPERTIES

Hydrophobicity(logP) 0.8
Solubility Soluble. 1-5 g/100 mL at 23 oC

DETAILS

Description (English)
Item Information
Drug Groups approved; investigational
Description Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the liver to form the active aldophosphamide. It has been used in the treatment of lymphoma and leukemia. Its side effect, alopecia, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. [PubChem]
Indication For management of malignant lymphomas, multiple myeloma,leukemias, mycosis fungoides (advanced disease), neuroblastoma (disseminated disease), adenocarcinoma of the ovary, retinoblastoma and carcinoma of the breast
Pharmacology Cyclophosphamide is an antineoplastic in the class of alkylating agents and is used to treat various forms of cancer. Alkylating agents are so named because of their ability to add alkyl groups to many electronegative groups under conditions present in cells. They stop tumor growth by cross-linking guanine bases in DNA double-helix strands - directly attacking DNA. This makes the strands unable to uncoil and separate. As this is necessary in DNA replication, the cells can no longer divide. In addition, these drugs add methyl or other alkyl groups onto molecules where they do not belong which in turn inhibits their correct utilization by base pairing and causes a miscoding of DNA. Alkylating agents are cell cycle-nonspecific. Alkylating agents work by three different mechanisms all of which achieve the same end result - disruption of DNA function and cell death.
Toxicity infection, myelosuppression, and cardiac toxicity
Affected Organisms
Humans and other mammals
Biotransformation hepatic
Absorption 90-100%
Half Life 3-12 hours
Protein Binding >60%
Elimination It is eliminated primarily in the form of metabolites, but from 5% to 25% of the dose is excreted in urine as unchanged drug.
References
Brock N: The history of the oxazaphosphorine cytostatics. Cancer. 1996 Aug 1;78(3):542-7. [Pubmed]
Brock N: Oxazaphosphorine cytostatics: past-present-future. Seventh Cain Memorial Award lecture. Cancer Res. 1989 Jan 1;49(1):1-7. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

REFERENCES

  • Brock N: The history of the oxazaphosphorine cytostatics. Cancer. 1996 Aug 1;78(3):542-7. Pubmed
  • Brock N: Oxazaphosphorine cytostatics: past-present-future. Seventh Cain Memorial Award lecture. Cancer Res. 1989 Jan 1;49(1):1-7. Pubmed