Synthesis and Aldose Reductase-Inhibitory Activity of Benzo[b]furan Derivatives Possessing a Carboxymethylsulfamoyl Group
スポンサーリンク
概要
- 論文の詳細を見る
Various benzo[b]futran derivatives with a carboxymethylsulfamoyl group were prepared and evaluated for aldose reductase-inhibitory potency. Most of the compounds displayed significant inhibitory activities (IC_<50>, 10^<-8>-10^<-7>M). Among the test compounds, the compounds having a carboxymethylsulfamoyl group at the 3- or 4-position exhibited the greatest inhibitory potency. Structure-activity trends of the tested compounds are discussed.
- 公益社団法人日本薬学会の論文
- 1989-09-25
著者
-
大石 義孝
Central Research Institute, Kaken Pharmaceutical Co., Ltd.,
-
大石 義孝
Central Research Institute Kaken Pharmaceutical Co. Ltd.
-
矢嶋 基之
Central Research Institute Kaken Pharmaceutical Co. Ltd.
-
永原 美知子
Central Research Institute, Kaken Pharmaceutical Co., Ltd.,
-
向井 輝夫
Central Research Institute, Kaken Pharmaceutical Co., Ltd.,
-
梶川 憲男
Central Research Institute, Kaken Pharmaceutical Co., Ltd.,
-
梶川 憲男
Central Research Institute Kaken Pharmaceutical Co. Ltd.
-
永原 美知子
Central Research Institute Kaken Pharmaceutical Co. Ltd.
-
向井 輝夫
Central Research Institute Kaken Pharmaceutical Co. Ltd.
関連論文
- Synthesis and Evaluation of (Piperidinomethylene)bis(phosphonic acid) Derivatives as Anti-osteoporosis Agents
- Elimination of 3-Hydroxy-2-nitro-2,3-dihydrobenzo[b]furans to 2-Nitrobenzo[b]furans
- A TYPICAL ELcB PROCESS IN THE ELIMINATION OF 3-HYDROXY-2-NITRO-2,3-DIHYDROBENZO [b] FURANS TO 2-NITROBENZO [b] FURANS
- Reactions of Salicylaldehydes with Bromonitromethane
- Synthesis and Antiallergic Activity of Novel Azaazulene Derivatives
- Preparations of 5-Alkylmethylidene-3-carboxymethylrhodanine Derivatives and Their Aldose Reductase Inhibitory Activity
- Stereoselective Synthesis of (E)-11-(2-Chloroethylidene)-6,11-dihydrodibenzo[b, e]thiepin
- Reaction of Epichlorohydrin with Hydroxybenzo[b]furan
- Preparation of 5-Alkyl-3-carboxymethylrhodanines and Their Aldose Reductase Inhibitory Activity
- Synthesis and Aldose Reductase-Inhibitory Activity of Benzo[b]furan Derivatives Possessing a Carboxymethylsulfamoyl Group