Skip to main content
An official website of the United States government
Government Funding Lapse
Because of a lapse in government funding, the information on this website may not be up to date, transactions submitted via the website may not be processed, and the agency may not be able to respond to inquiries until appropriations are enacted.

The NIH Clinical Center (the research hospital of NIH) is open. For more details about its operating status, please visit cc.nih.gov.

Updates regarding government operating status and resumption of normal operations can be found at opm.gov.

thiotepa

View Patient Information
A polyfunctional, organophosphorus alkylating agent and a stable derivative of N,N',N''-triethylenephosphoramide (TEPA), with antineoplastic activity. Upon administration, thiotepa is converted into highly reactive ethylenimine groups, which covalently bind to nucleophilic groups in DNA and demonstrate a preference for the N7 position of guanine bases. This induces crosslinking of alkylated guanine bases in double-stranded DNA, interferes with both DNA replication and cell division, and results in both the induction of apoptosis and the inhibition of cell growth.
Synonym:thiofosfamide
thiophosphamide
thiophosphoamide
thiophosphoramide
triethylene thiophosphoramide
triethylenethiophosphoramide
US brand name:Tepadina
Tepylute
Abbreviation:TESPA
TSPA
Code name:SH 105
SH-105
SH105
WR 45312
Chemical structure:1,1',1''-phosphinothioyldynetrisaziridine
1,1',1"-phosphinothioylidynetrisaziridine
N,N',N''-triethylenethiophosphoramide
tris(1-aziridinyl)phosphine sulfide
Search NCI's Drug Dictionary