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Bioorg Med Chem Lett ; 15(10): 2491-4, 2005 May 16.
Article in English | MEDLINE | ID: mdl-15863303

ABSTRACT

To overcome pharmacokinetic and solubility problems observed in early clinical trials with the potent anticancer compound CHS828, we synthesised a series of prodrugs with improved properties. The best compound obtained was EB1627, with a tetraethyleneglycol moiety attached to the parent drug via a carbonate linkage. This compound was found soluble enough to be given i.v. and the drug was rapidly released in vivo exerting a very potent inhibitory activity alone and in combination with known cytostatics (etoposide) in animal models in vivo.


Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Prodrugs/chemistry , Antineoplastic Agents/pharmacokinetics , Cell Line, Tumor , Clinical Trials as Topic , Drug Screening Assays, Antitumor , Humans , Prodrugs/pharmacokinetics
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