Lahiri S, Gupta J K, Mondal A K
J Pharm Sci. 1975 Jan;64(1):172-4. doi: 10.1002/jps.2600640144.
A number of indanamines substituted at the terminal amino nitrogen with various aliphatic, alicyclic, heterocyclic, and aromatic ring systems were synthesized and screened for hypoglycemic activity. None was found to possess significant activity compared to tolbutamide.
合成了一系列在末端氨基氮上被各种脂肪族、脂环族、杂环和芳环系统取代的茚胺，并对其降血糖活性进行了筛选。与甲苯磺丁脲相比，未发现有任何一种具有显著活性。
