Title of article
Synthesis of acyloxymethyl ester prodrugs of the transferable protein farnesyl transferase substrate farnesyl methylenediphosphonate
Author/Authors
Jerry M. Troutman، نويسنده , , Kareem A.H. Chehade، نويسنده , , Katarzyna Kiegiel، نويسنده , , Douglas A. Andres، نويسنده , , H. Peter Spielmann، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
4
From page
4979
To page
4982
Abstract
Three isoprenoid diphosphate analogues of farnesyl diphosphate (FPP) where the diphosphate has been replaced by methylene diphosphonate and the negative charges masked by frangible pivaloyloxymethyl (POM) esters were prepared. Farnesyl methylenediphosphonate is a sub-micromolar substrate for protein farnesyl transferase. The tripivaloyloxymethyl esters of isoprenoid methylenediphosphonate have significantly increased lipophilicity and may act as important farnesyl diphosphate prodrugs.
Keywords
e-mail: hps@uky.edu , Prodrugs.* Corresponding author. Tel.: +1-859-2574790 , Bisphosphonates , fax: +1-859-2578940 , Farnesylation
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2004
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
794911
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