机译:DNA模板的小分子文库的体外选择揭示了一类大环激酶抑制剂。
Department of Chemistry and Chemical Biology and the Howard Hughes Medical Institute,Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138;
rnDepartment of Chemistry and Chemical Biology and the Howard Hughes Medical Institute,Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138;
rnDepartment of Chemistry and Chemical Biology and the Howard Hughes Medical Institute,Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138;
rnDepartment of Chemistry and Chemical Biology and the Howard Hughes Medical Institute,Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138;
rnDepartment of Chemistry and Chemical Biology and the Howard Hughes Medical Institute,Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138;
机译:DNA模板的小分子文库的体外选择揭示了一类大环激酶抑制剂。
机译:从DNA编码的小分子文库×蛋白质文库选择中发现共价激酶抑制剂
机译:吲哚美辛文库的合成和生物学评估揭示了一类新的与血管生成有关的激酶抑制剂。
机译:具有构象多样性的小肽致癌致癌物质文库的新合成:IGF-1R抑制剂的发现
机译:迭代分支途径:一种通过DNA模板合成实现访问各种小分子文库的策略。
机译:DNA模板的小分子文库的体外选择揭示了一类大环激酶抑制剂。
机译:DNA模板的小分子文库的体外选择揭示了一类大环激酶抑制剂。