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Amifostine

产品号 DB01143 公司名称 DrugBank
CAS号 20537-88-6 公司网站 http://www.ualberta.ca/
分子式 C5H15N2O3PS 电 话 (780) 492-3111
分子量 214.222961 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 1014

产品价格信息

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产品别名

标题
Amifostine
IUPAC标准名
({2-[(3-aminopropyl)amino]ethyl}sulfanyl)phosphonic acid
IUPAC传统名
amifostine
商标名
Ethyol
别名
Ethiofos
SAPEP
Gammaphos
WR-1065
Amifostine Ethiofos
Aminopropylaminoethyl Thiophosphate
Apaetp
amifostine

产品登记号

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

产品性质

疏水性(logP) -1.9
溶解度 1000 mg/mL

产品详细信息

详细说明 (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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参考文献

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