Cyclopropane-Based Stereochemical Diversity-Oriented Conformational Restriction Strategy : Histamine Analogs with the 4-Amino-2, 3-methano-1-(1H-imidazol-4-yl)butane Structure as Highly Potent Histamine H3 and/or H4 Receptor Ligands.
Cyclopropane-Based Stereochemical Diversity-Oriented Conformational Restriction Strategy : Histamine Analogs with the 4-Amino-2, 3-methano-1-(1H-imidazol-4-yl)butane Structure as Highly Potent Histamine H3 and/or H4 Receptor Ligands.
复制标题
基于环丙烷的立体化学多样性导向的构象限制策略：具有 4-Amino-2, 3-methano-1-(1H-imidazol-4-yl)butane 结构的组胺类似物作为高效组胺 H3 和/或 H4 受体配体。
DOI：
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发表时间：
2012
期刊：
影响因子：
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通讯作者：
S. Shuto
中科院分区：
文献类型：
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作者：
M. Watanabe;T. Kobayashi;T. Hirokawa;A. Yoshida;Y. Ito;S. Yamada;N. Orimoto;Y. Yamasaki;M. Arisawa;S. Shuto
