Bioactivatable derivatives of 8-substituted cAMP-analogues
摘要:
Four 8-substituted derivatives of cAMP were converted into their membrane-permeant acetoxymethyl esters (AM-esters). The activity of these bioactivatable compounds to induce chloride secretion of T-84 cells was up to 100-fold increased compared to the non-modified cAMP derivatives. (C) 1997 Elsevier Science Ltd.
Bioactivatable derivatives of 8-substituted cAMP-analogues
作者:Jens Kruppa、Stephen Keely、Frank Schwede、Carsten Schultz、Kim E. Barrett、Bernd Jastorff
DOI:10.1016/s0960-894x(97)00136-4
日期:1997.1
Four 8-substituted derivatives of cAMP were converted into their membrane-permeant acetoxymethyl esters (AM-esters). The activity of these bioactivatable compounds to induce chloride secretion of T-84 cells was up to 100-fold increased compared to the non-modified cAMP derivatives. (C) 1997 Elsevier Science Ltd.