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Chlorambucil

Catalog No. DB00291 Name DrugBank
CAS Number 305-03-3 Website http://www.ualberta.ca/
M. F. C14H19Cl2NO2 Telephone (780) 492-3111
M. W. 304.21216 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 176

SYNONYMS

IUPAC name
4-{4-[bis(2-chloroethyl)amino]phenyl}butanoic acid
IUPAC Traditional name
chlorambucil
Brand Name
Linfolizin
Amboclorin
Ecloril
Elcoril
Leukeran
Leukeran Tablets
Leukersan
Leukoran
Pepstatin
Ambochlorin
Linfolysin
Synonyms
Chloroambucil
Chlorobutine
Chlorobutin
Chlorbutine
Chlorbutin
Chloraminophen
Phenylbutyric Acid Nitrogen Mustard
Chlocambucil
Chloraminophene

DATABASE IDS

PubChem CID 2708
PubChem SID 46506842
CAS Number 305-03-3

PROPERTIES

Hydrophobicity(logP) 3.9
Solubility 1.24E+004 mg/L

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A nitrogen mustard alkylating agent used as antineoplastic agent for the treatment of various malignant and nonmalignant diseases. Although it is less toxic than most other nitrogen mustards, it has been listed as a known carcinogen in the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (Merck Index, 11th ed)
Indication For treatment of chronic lymphatic (lymphocytic) leukemia, childhood minimal-change nephrotic syndrome, and malignant lymphomas including lymphosarcoma, giant follicular lymphoma, Hodgkin's disease, non-Hodgkin's lymphomas, and Waldenstr?m’s Macroglobulinemia.
Pharmacology Chlorambucil is an antineoplastic in the class of alkylating agents that 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.
Affected Organisms
Humans and other mammals
Half Life 1.5 hours
Protein Binding 99%
Elimination Chlorambucil is extensively metabolized in the liver primarily to phenylacetic acid mustard. The pharmacokinetic data suggests that oral chlorambucil undergoes rapid gastrointestinal absorption and plasma clearance and that it is almost completely metabolized, having extremely low urinary excretion.
References
Rai KR, Peterson BL, Appelbaum FR, Kolitz J, Elias L, Shepherd L, Hines J, Threatte GA, Larson RA, Cheson BD, Schiffer CA: Fludarabine compared with chlorambucil as primary therapy for chronic lymphocytic leukemia. N Engl J Med. 2000 Dec 14;343(24):1750-7. [Pubmed]
Yang K, Tan J, Wu T: Alkylating agents for Waldenstrom's macroglobulinaemia. Cochrane Database Syst Rev. 2009 Jan 21;(1):CD006719. [Pubmed]
Foon KA, Hallek MJ: Changing paradigms in the treatment of chronic lymphocytic leukemia. Leukemia. 2010 Mar;24(3):500-11. Epub 2009 Dec 24. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com

REFERENCES

  • Rai KR, Peterson BL, Appelbaum FR, Kolitz J, Elias L, Shepherd L, Hines J, Threatte GA, Larson RA, Cheson BD, Schiffer CA: Fludarabine compared with chlorambucil as primary therapy for chronic lymphocytic leukemia. N Engl J Med. 2000 Dec 14;343(24):1750-7. Pubmed
  • Yang K, Tan J, Wu T: Alkylating agents for Waldenstrom's macroglobulinaemia. Cochrane Database Syst Rev. 2009 Jan 21;(1):CD006719. Pubmed
  • Foon KA, Hallek MJ: Changing paradigms in the treatment of chronic lymphocytic leukemia. Leukemia. 2010 Mar;24(3):500-11. Epub 2009 Dec 24. Pubmed