Overcoming mutagenicity and ion channel activity: optimization of selective spleen tyrosine kinase inhibitors.
第一作者:
J Michael,Ellis
第一单位:
Department of Discovery Chemistry, ‡Department of Process Research, §Department of Immunology, ∥Department of Pharmacology, ⊥Department of Pharmacokinetics, Pharmacodynamics, and Drug Metabolism, #Department of Safety Assessment and Laboratory Animal Resources, and ▽Department of Discovery Pharmaceutical Sciences, Merck & Co., Inc. , 33 Avenue Louis Pasteur, Boston, Massachusetts 02115, United States.
作者:
医学主题词
酰胺类(Amides);结晶学, X线(Crystallography, X-Ray);剂量效应关系, 药物(Dose-Response Relationship, Drug);快速延迟整流钾通道(Ether-A-Go-Go Potassium Channels);人类(Humans);模型, 分子(Models, Molecular);分子结构(Molecular Structure);诱变力试验(Mutagenicity Tests);蛋白激酶抑制剂(Protein Kinase Inhibitors);蛋白酪氨酸激酶类(Protein-Tyrosine Kinases);脾(Spleen);构效关系(Structure-Activity Relationship)
DOI
10.1021/jm5018169
PMID
25625541
发布时间
2015-02-26
- 浏览28
Journal of medicinal chemistry
1929-39页
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