Synthesis and SAR studies of benzimidazolone derivatives as histamine H3-receptor antagonists
作者:Qingbei Zeng、Stuart B. Rosenblum、Zhaoxia Yang、Yueheng Jiang、Kevin D. McCormick、Robert G. Aslanian、Luli Duguma、Joseph A. Kozlowski、Neng-Yang Shih、John A. Hey、Robert E. West、Walter A. Korfmacher、Michael Berlin、Christopher W. Boyce
DOI:10.1016/j.bmcl.2013.08.012
日期:2013.11
A novel series of benzimidazolone-containing histamineH3-receptor antagonists were prepared and their structure–activity relationship was explored. These benzimidazolone analogs demonstrate potent H3-receptor binding affinities, no P450 enzyme inhibition, and strong H3 functional activity. Compound 1o exhibits the best overall profile with H3Ki = 0.95 nM and rat AUC = 12.9 μM h.
制备了一系列新的含苯并咪唑酮的组胺H 3受体拮抗剂,并探讨了它们的结构-活性关系。这些苯并咪唑酮类似物显示出有效的H 3-受体结合亲和力,无P450酶抑制作用,并且具有强大的H 3功能活性。化合物1o表现出最佳的总体特征,H 3 K i = 0.95 nM,大鼠AUC = 12.9μMh。
Fluoride-mediated selective cross-coupling reactions of alkyl halides and trimethyl(perfluoroalkyl)silanes, Me3SiRf (Rf=CF3, C2F5) in the absence of any catalysts
作者:Wieland Tyrra、Dieter Naumann、Silke Quadt、Sigrid Buslei、Yurii L. Yagupolskii、Mikhail M. Kremlev
DOI:10.1016/j.jfluchem.2007.02.017
日期:2007.7
A temperature range of −18 °C to room temperature was found to be effective for selective fluoride-mediated cross-couplingreactions of trimethyl(perfluoroalkyl)silanes, Me3SiCF3 and Me3SiC2F5, and alkyl halides, RX (X = Br, I) in the absence of any catalyst.
已发现在−18°C到室温的温度范围内对于三甲基(全氟烷基)硅烷Me 3 SiCF 3和Me 3 SiC 2 F 5以及烷基卤化物RX( X = Br,I)在没有任何催化剂的情况下。
Hydroxy substituted polyfluorinated compounds
申请人:EASTMAN KODAK CO
公开号:US02700686A1
公开(公告)日:1955-01-25
Azo compounds containing a hydroxy substituted polyfluorinated group