Azole Derivatives As Histamine H3 Receptor Antagonists, Part 2: C–C and C–S Coupled Heterocycles
Bioorganic & medicinal chemistry letters(2010)
摘要
With a small series of compounds we demonstrated the variability in the core region of the human histamine H(3) receptor (hH(3)R) antagonist structural blueprint by introducing polar azole groups (oxazole, oxadiazole, thiazole and triazole). Additional variations achieved by coupling different residues to the heterocyclic core structure led to further optimisation of in vitro receptor binding of the novel azole derivatives.
更多查看译文
关键词
GPCR,Histamine,H3,Pharmacophore,Medicinal chemistry,Bioisosteric replacement
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要