19130-96-2OCC1NCC(O)C(O)C1OLXBIFEVIBLOUGU-UHFFFAOYSA-N1-deoxynojirimycin (unspec. stereochemistry) has been reported in Bacillus subtilis, Commelina, and other organisms with data available.
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
解説デオキシノジリマイシン,1,5-dideoxy-1,5-imino-glucitol.C6H13NO4(163.17).クワMorusやJacobinia suberectaから単離され,また,種々の桿(かん)状菌が生産するアルカロイド.α-グルコシダーゼ阻害剤.抗高血糖症活性があり,家畜の飼料などに添加される.抗HIV活性も報告されている.融点206°.[α]D+44.7°(水).
用途糖たん白質糖鎖合成過程、生物機能の解析ツール。
天然物の起源1-Deoxynojirimycin (DNJ), a product of fermentation, exists in mulberry leaves and Commelina communis (dayflower) as well as is isolated from several bacterial strains such as Bacillus and Streptomyces species. Mulberry, a common deciduous plant, belongs to the genus Morus (Moraceae family). Numerous researchers have reported the DJN contents in different parts and various varieties of mulberry. Various mulberry varieties contain DNJ contents ranging between 0.68 and 2.78 mg/gm, while this fraction varies between 1.57 and 3.48 mg/gm in different Chinese mulberry leaves. Moreover, mulberry shoots contain the highest contents of DNJ, followed by young mulberry leaves. Mature leaves of mulberry contain the least content of DNJ. All the mulberry leave groups showed a 1–2-fold increase in DNJ contents compared to unfermented mulberry leaf powder extract (UFMLE). Additionally, fermented mulberry leaf powder extract exhibited higher α-glucosidase activity than UFMLE. DNJ-rich food products can be prepared by fermenting mulberry leaves using the above-mentioned fermenting agents[6].
使用An alpha-glucosidase inhibitor. Interferes with normal processing of N-linked glycoproteins.(+)-1-Deoxynojirimycin acts as an inhibitor of alfa-glucosidase I and II and maltase-glucoamylase. It also inhibits mammalian glucosidase, intestinal and lysosmal, beta-glucosidase from sweet almonds, pancreatic alfa-amylase and amyloglucosidase. Further, it serves as a enzyme enhancer for the treatment of Fabry and Pompe disease.
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19130-96-2CHEMBL11510化学的特性White Crystalline Solid
定義ChEBI: An optically active form of 2-(hydroxymethyl)piperidine-3,4,5-triol having 2R,3R,4R,5S-configuration.