已经描述了由容易获得的邻甲酰基-芳基酮和芳基/(杂)芳基甲胺有效和碱介导的一锅区域特异性合成结构上多样化的异喹啉和苯并[ h ]异喹啉。通过这种发达的化学方法很容易获得具有挑战性的3-炔基/烯基异喹啉和双异喹啉,它们可进一步用于各种有机转化。操作简便,高原子经济性,广泛的底物范围,官能团耐受性和对大规模合成的适用性是此开发方法的优势。
已经描述了由容易获得的邻甲酰基-芳基酮和芳基/(杂)芳基甲胺有效和碱介导的一锅区域特异性合成结构上多样化的异喹啉和苯并[ h ]异喹啉。通过这种发达的化学方法很容易获得具有挑战性的3-炔基/烯基异喹啉和双异喹啉,它们可进一步用于各种有机转化。操作简便,高原子经济性,广泛的底物范围,官能团耐受性和对大规模合成的适用性是此开发方法的优势。
Design of an Anticancer Copper(II) Prodrug Based on the Lys199 Residue of the Active Targeting Human Serum Albumin Nanoparticle Carrier
作者:Yi Gou、Yao Zhang、Zhenlei Zhang、Jun Wang、Zuping Zhou、Hong Liang、Feng Yang
DOI:10.1021/acs.molpharmaceut.6b01074
日期:2017.6.5
which will decrease its anticancer activity relative to the original metal agent. Thus, to improve the delivery efficiency of the metal agent and simultaneously avoid decreasing its anticancer activity in vivo, we decided to develop an anticancer metal prodrug by regulating its pharmacophore ligand so that it would not be displaced by the Lys199 residue of the folic acid (FA)-functionalized HSA nanoparticle