Defining The Molecular Requirements For The Selective Delivery Of Polyamine Conjugates Into Cells Containing Active Polyamine Transporters
Several N1-substituted polyamines containing various spacer units between nitrogen centers were synthesized as their respective HCl salts. The N1-substituents included benzyl, naphthalen-1-ylmethyl, anthracen-9-ylmethyl, and pyren-1-ylmethyl. The polyamine spacer units ranged from generic (4,4-triamine, 4,3-triamine, and diaminooctane) spacers to more exotic [2-(ethoxy)ethanoxy-containing diamine, hydroxylated 4,3-triamine, and cyclohexylene-containing triamine] spacers. Two control compounds were also evaluated: N-(anthracen-9-ylmethyl)-butylamine and N-(anthracen-9-ylmethyl)-butanediamine. Biological activities in L1210 (murine leukemia), α-difluoromethylornithine (DFMO)-treated L1210, and Chinese hamster ovary (CHO) and its polyamine transport-deficient mutant (CHO-MG) cell lines were investigated via IC50 cytotoxicity determinations. K i values for spermidine uptake were also determined in L1210 cells. Of the series studied, the N1-benzyl-4,4-triamine system 6 had significantly higher IC50 values (lower cytotoxicity) in the L1210, CHO, and CHO-MG cell lines. A cellular debenzylation process was observed in L1210 cells with 6 and generated "free" homospermidine. The size of the N1-arylmethyl substituent had direct bearing on the observed cytotoxicity in CHO-MG cells. The N1-naphthalenylmethyl, N′-anthracenylmethyl, and N′-pyrenylmethyl 4,4-triamines had similar toxicity (IC50s: ∼0.5 μM) in CHO cells, which have an active polyamine transporter (PAT). However, this series had IC50 values of > 100 μM, 66.7 μM, and 15.5 μM, respectively, in CHO-MG cells, which are PAT-deficient. The observed lower cytotoxicity in the PAT-deficient CHO-MG cell line supported the premise that the conjugates use PAT for cellular entry. In general, moderate affinities for the polyamine transporter were observed for the N-arylmethyl 4,4-triamine series with their L1210 Ki values all near 3 μM. In summary, the 4,4-triamine motif was shown to facilitate entry of polyamine conjugates into cells containing active polyamine transporters.
Journal of Medicinal Chemistry
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Wang, Chaojie; Delcros, Jean Guy; and Cannon, Laura, "Defining The Molecular Requirements For The Selective Delivery Of Polyamine Conjugates Into Cells Containing Active Polyamine Transporters" (2003). Scopus Export 2000s. 1512.