Johann Wolfgang Goethe University, Institute of Pharmaceutical Chemistry, Biocenter, Max-von-Laue-Strasse 9, 60438 Frankfurt am Main, Germany.
Org Lett. 2010 Jun 4;12(11):2578-81. doi: 10.1021/ol100419y.
Iron-containing ligands targeting the human histamine H(3) receptor (hH(3)R) were prepared. The compounds contain ferrocene sandwich complexes coupled via different linkers to a basic hH(3)R antagonist/inverse agonist pharmacophore. In a click chemistry approach, a triazole was successfully inserted as a new linking element. Two ferrocenylmethylamines and a ferrocenyltriazole were the most affine hH(3)R ligands within this series, showing receptor binding in the nano- and subnanomolar concentration range.
本文制备了含铁配体,用于靶向人组氨酸 H(3) 受体(hH(3)R)。这些化合物包含通过不同连接子偶联的二茂铁夹心复合物,连接到碱性 hH(3)R 拮抗剂/反向激动剂药效团。在点击化学方法中,成功插入三唑作为新的连接元素。在该系列中,两种二茂铁甲胺和一种二茂铁三唑是最亲和的 hH(3)R 配体,在纳摩尔和亚纳摩尔浓度范围内显示出受体结合。