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Block of cyclic nucleotide-gated channels by tetracaine derivatives: role of apolar interactions at two distinct locations

T Strassmaier, SR Kirk, T Banerji, JW Karpen

文献索引:Strassmaier, Timothy; Kirk, Sarah R.; Banerji, Tapasree; Karpen, Jeffrey W. Bioorganic and Medicinal Chemistry Letters, 2008 , vol. 18, # 2 p. 645 - 649

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被引用次数: 2

摘要

A series of new tetracaine derivatives was synthesized to explore the effects of hydrophobic character on blockade of cyclic nucleotide-gated (CNG) channels. Increasing the hydrophobicity at either of two positions on the tetracaine scaffold, the tertiary amine or the butyl tail, yields blockers with increased potency. However, shape also plays an important role. While gradual increases in length of the butyl tail lead to increased potency, ...