机译:通过使用优化的潜入硫酯固相接头,通过可推广的方法的合成和生物学评价通过概括的方法进行倍增方法
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Biol Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Biol Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Christopher Newport Univ Dept Mol Biol &
Chem Newport News VA 23606 USA;
Christopher Newport Univ Dept Mol Biol &
Chem Newport News VA 23606 USA;
Christopher Newport Univ Dept Mol Biol &
Chem Newport News VA 23606 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Biol Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
Christopher Newport Univ Dept Mol Biol &
Chem Newport News VA 23606 USA;
Hobart &
William Smith Coll Dept Biol Geneva NY 14456 USA;
Hobart &
William Smith Coll Dept Chem Geneva NY 14456 USA;
机译:通过使用优化的潜入硫酯固相接头,通过可推广的方法的合成和生物学评价通过概括的方法进行倍增方法
机译:使用MultiSep虚拟筛选方法鉴定潜在组蛋白脱甲酰化酶1(HDAC1)抑制剂,包括SVM模型,药物模型,分子对接和生物学评估
机译:CD [L-脯氨酸] 2的合成,表征和评价,一种新型组蛋白脱乙酰酶抑制剂,其在A549细胞中诱导组蛋白脱乙酰酶同种型的表观遗传改性
机译:L-2-氨基-7 / 8-溴烷酸衍生物作为组蛋白脱乙酰酶抑制剂的合成,评价和分子建模研究
机译:组蛋白脱乙酰基酶抑制剂Largazole及其类似物的合成及生物学评价
机译:新型基于香豆素的异羟肟酸酯衍生物作为具有抗肿瘤活性的组蛋白脱乙酰基酶(Hdac)抑制剂的设计合成和生物学评估
机译:通过使用优化的潜入硫酯固相接头,通过可推广的方法的合成和生物学评价通过概括的方法进行倍增方法