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Amifostine

Catalog No. DB01143 Name DrugBank
CAS Number 20537-88-6 Website http://www.ualberta.ca/
M. F. C5H15N2O3PS Telephone (780) 492-3111
M. W. 214.222961 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 1014

SYNONYMS

IUPAC name
({2-[(3-aminopropyl)amino]ethyl}sulfanyl)phosphonic acid
IUPAC Traditional name
amifostine
Brand Name
Ethyol
Synonyms
Ethiofos
SAPEP
Gammaphos
WR-1065
Amifostine Ethiofos
Aminopropylaminoethyl Thiophosphate
Apaetp
amifostine

DATABASE IDS

PubChem SID 46505305
PubChem CID 2141
CAS Number 20537-88-6

PROPERTIES

Hydrophobicity(logP) -1.9
Solubility 1000 mg/mL

DETAILS

Description (English)
Item Information
Drug Groups approved; investigational
Description A phosphorothioate proposed as a radiation-protective agent. It causes splenic vasodilation and may block autonomic ganglia. [PubChem]
Indication For reduction in the cumulative renal toxicity in patients with ovarian cancer (using cisplatin) and moderate to severe xerostomia in patients undergoing post-operative radiation treatment for head and neck cancer.
Pharmacology Amifostine is an organic thiophosphate cytoprotective agent indicated to reduce the cumulative renal toxicity associated with repeated administration of cisplatin in patients with advanced ovarian cancer or non-small cell lung cancer and also to reduce the incidence of moderate to severe xerostomia in patients undergoing post-operative radiation treatment for head and neck cancer. Amifostine is a prodrug that is dephosphorylated by alkaline phosphatase in tissues to a pharmacologically active free thiol metabolite, believed to be responsible for the reduction of the cumulative renal toxicity of cisplatin and for the reduction of the toxic effects of radiation on normal oral tissues. Healthy cells are preferentially protected because amifostine and metabolites are present in healthy cells at 100-fold greater concentrations than in tumour cells.
Toxicity Rat LD50: 826 mg/kg
Affected Organisms
Humans and other mammals
Biotransformation Amifostine is rapidly dephosphorylated by alkaline phosphatase in tissues primarily to the active free thiol metabolite and, subsequently, to a less active disulfide metabolite.
Half Life 8 minutes
Elimination After a 10-second bolus dose of 150 mg/m2 of ETHYOL, renal excretion of the parent drug and its two metabolites was low during the hour following drug administration, averaging 0.69%, 2.64% and 2.22% of the administered dose for the parent, thiol and disulfide, respectively.
References
Santini V, Giles FJ: The potential of amifostine: from cytoprotectant to therapeutic agent. Haematologica. 1999 Nov;84(11):1035-42. [Pubmed]
External Links
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REFERENCES

  • Santini V, Giles FJ: The potential of amifostine: from cytoprotectant to therapeutic agent. Haematologica. 1999 Nov;84(11):1035-42. Pubmed