References
- Schmidt DD, Frommer W, Muller L, Truscheit E. 1979. Glucosidase-inhibitoren aus Bazillen. Naturwissenshaften 66: 584-585 https://doi.org/10.1007/BF00368825
- Yagi M, Kouno T, Aoyagi Y, Murai H. 1976. The structure of moranoline a piperidine alkaloid from Morus species. Nippon Nogeikagaku Kaish 50: 571-572 https://doi.org/10.1271/nogeikagaku1924.50.11_571
- Bischoff H. 1995. The mechanism of a-glucosidase inhibition in the management of diabetes. Chin Invest Med 18: 303-311
- Lembcke B, Folsch UR, Creutzfeldt W. 1985. Effect of 1-deoxynojirimycin derivatives on small intestinal disaccharidase activities and on active transport in vitro. Digestion 31: 120-127 https://doi.org/10.1159/000199188
- Asano N, Nash RJ, Molyneux RJ, George WJ. 2000. Sugar-mimic glycosidase inhibitors: natural occurrence, biological activity and prospects for therapeutic application. Tetrahedron: Asymmetry 11: 1645-1680 https://doi.org/10.1016/S0957-4166(00)00113-0
- Breitmeier D, Gunther S, Heymann H. 1997. Acarbose and 1-deoxynojirimycin inhibit maltose and maltooligosaccharide hydrolysis of human small intestinal glucoamylase-maltase in two different substrate-induced modes. Arch Biochem Biophys 346: 7-14 https://doi.org/10.1006/abbi.1997.0274
- Park SW, Song YD, Lee EJ, Lim SK, Kim KR, Lee HC, Huh KB, Chung YS. 1994. Effect of acarbose in NIDDM insufficiently treated with diet alone. Korean Diabetes J 18: 263-269
- Watanabe K, Uchino H, Ohmura C, Tanaka Y, Onuma T, Kawamori R. 2004. Different effects of two a-glucosidase inhibitors, acarbose and voglibose, on serum 1,5-anhydroglucitol (1,5AG) level. J Diabetes Complications 18: 183-186 https://doi.org/10.1016/S1056-8727(03)00055-2
-
Asano N, Kato A, Kizu H, Matsui KM, Watson A, Nash RJ. 1996. Calystegine
$B_4$ , a novel trehalase inhibitor from Scopolia japonica. Carbohydr Res 293: 195-382 https://doi.org/10.1016/0008-6215(96)00204-2 - Aasno N, Yamashita T, Yasuda K, Ikeda K. 2001. Polyhydroxylated alkaloids isolated from mulberry trees (Morus alba L.) and silkworms (Bombyx mori L.). J Agric Food Chem 49: 4208-4213 https://doi.org/10.1021/jf010567e
- Aasno N, Nishida M, Miyauchi M, Ikeda K. 2000. Polyhydroxylated pyrrolidine and piperidine alkaloids from Adenophora triphylla var. japonica (Campanulaceae). Phytochemistry 53: 397-382 https://doi.org/10.1016/S0031-9422(99)00555-5
- Evans SV, Fellow LE, Shing TKM, Fleet GWJ. 1985. Glycosidase inhibition by plant alkaloids which are structural analogues of monosaccharides. Phytochemistry 24: 1953-1955 https://doi.org/10.1016/S0031-9422(00)83099-X
- Murao S, Miyata S. 1980. Isolation and characterization of a new trehalase inhibitor, S-GI. Agric Biol Chem 44: 219-221 https://doi.org/10.1271/bbb1961.44.219
- Yamada H, Oya I, Nagai T. 1993. Screening of a-glucosidase II inhibitor from Chinese herbs and its application on the quality control of mulberry bark. Shoyakugaku Zasshi 47: 47-55
- Ezure Y, Maruo S, Miyazaki K, Kawamata M. 1985. Moranoline (1-deoxynojirimycin) fermentation and its improvement. Agric Biol chem 49: 1119-1125 https://doi.org/10.1271/bbb1961.49.1119
- Hardick DJ, Hutchinson DW, Trew SJ, Wellington EMH. 1992. Glucose is a precursor of 1-deoxynojirimycin and 1-deoxymannonojirimycin in Streptomyces subrutilus. Tetrahedron 48: 6285-6296 https://doi.org/10.1016/S0040-4020(01)88220-X
- Hardick DJ, Hutchinson DW. 1993. The biosynthesis of 1-deoxynojirimycin in Bacillus subtilis var niger. Biochemistry 49: 6707-6716 https://doi.org/10.1016/S0040-4020(01)81840-8
- Paek NS, Kang DS, Choi YJ, Lee JJ, Kim TH, Kim KW. 1997. Production of 1-deoxynojirimycin by Streptomyces sp. SID9135. J Microbiol Biochnol 7: 262-266
- Scofield AM, Fellow LE, Nash RJ, Fleet GWJ. 1986. Inhibition of mammalian digestive disaccharidases by polyhydroxy alkaloids. Life Sci 39: 29-32 https://doi.org/10.1016/0024-3205(86)90046-9
- Werner F, Lutz M, Delf S, Krause HP. 1981. Inhibitors, obtained from bacilli, for glycoside hydrolases. US Patent 4307194
- Kim JW, Kim SU, Lee HS. 2003. Determination of 1-deoxynojirimycin in Morus alba L. leaves by derivatization with 9-fluorenylmethyl chloroformate followed by reversedphase high-performance liquid chromatography. Chromatography 1002: 93-99 https://doi.org/10.1016/S0021-9673(03)00728-3
- Kim MS, Choue RW, Chung SH, Koo SJ. 1998. Blood glucose lowering effects of mulberry leaves and silkworm extracts on mice fed with high-carbohydrate diet. Korean J Nutrition 31: 117-125
- Kim SH, Kim KS, Lee JH, Chung EK, Park YS, Park YJ, Lee HY. 1997. Comparison of glucose-lowering activity of the extracts from Kangwon-do mountain mulberry leaves (Mori Folium) and silk worm. Kor J Appl Microbiol Biotechnol 25: 391-395
- Lee HS, Chung KS, Kim SY, Ryu KS, Lee WC. 1998. Effect of several sericultural products on blood glucose lowering for alloxan-induced hyperglycemic mice. Korean J Seric Sci 40: 38-42
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