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136 related items for PubMed ID: 8431930
1. Syntheses of modified 2-chloro-4-nitrophenyl beta-maltopentaosides as useful substrates for assay of human alpha amylase. Tokutake S, Uchida R, Kotani K, Saito K, Yamaji N. Carbohydr Res; 1993 Jan 15; 238():109-33. PubMed ID: 8431930 [Abstract] [Full Text] [Related]
2. Syntheses of subtractively modified 2-chloro-4-nitrophenyl beta-maltopentaosides and their application to the differential assay of human alpha-amylases. Tokutake S, Oguma T, Tobe K, Kotani K, Saito K, Yamaji N. Carbohydr Res; 1993 Jan 15; 238():193-213. PubMed ID: 8431933 [Abstract] [Full Text] [Related]
4. Preparation of non-reducing-end substituted p-nitrophenyl alpha-maltopentaoside (FG5P) as a substrate for a coupled enzymatic assay for alpha-amylases. Omichi K, Ikenaka T. J Biochem; 1985 Apr 15; 97(4):977-82. PubMed ID: 3161874 [Abstract] [Full Text] [Related]
5. Systematic synthesis of sulfur-containing p-nitrophenyl alpha-maltopentaoside derivatives for a differential assay of human alpha-amylases. Ozawa K, Taki Y, Ishida H, Yamagata Y, Satomura S, Kiso M, Hasegawa A. Biosci Biotechnol Biochem; 1993 May 15; 57(5):821-8. PubMed ID: 7763778 [Abstract] [Full Text] [Related]
6. Studies on the substrate specificity of Taka-amylase A1. XIV. Preparation of 6-deoxy-6-halogenomaltotrioses and their hydrolysis by Taka-amylase A. Omichi K, Matsushima Y. J Biochem; 1978 Oct 15; 84(4):835-41. PubMed ID: 309468 [Abstract] [Full Text] [Related]
9. Alpha-amylase assay with use of a benzyl derivative of p-nitrophenyl alpha-maltopentaoside, BG5P. Satomura S, Sakata Y, Omichi K, Ikenaka T. Clin Chim Acta; 1988 Jun 15; 174(3):315-23. PubMed ID: 3134147 [Abstract] [Full Text] [Related]
10. Synthesis of O-alpha-D-glucopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-D-glucopyranose as a substrate analogue of alpha amylase. Takeo K, Nakagen M, Teramoto Y, Nitta Y. Carbohydr Res; 1990 Jul 01; 201(2):261-75. PubMed ID: 2224882 [Abstract] [Full Text] [Related]
11. Chemical synthesis of 6'-alpha-maltosyl-maltotriose, a branched oligosaccharide representing the branch point of starch. Motawia MS, Olsen CE, Enevoldsen K, Marcussen J, Møller BL. Carbohydr Res; 1995 Nov 07; 277(1):109-23. PubMed ID: 8548783 [Abstract] [Full Text] [Related]
12. Synthesis of methyl glycoside derivatives of tri- and penta-saccharides related to the antithrombin III-binding sequence of heparin, employing cellobiose as a key starting-material. Ichikawa Y, Monden R, Kuzuhara H. Carbohydr Res; 1988 Jan 15; 172(1):37-64. PubMed ID: 3349502 [Abstract] [Full Text] [Related]
13. Transglycosylation reaction of maltotriose-forming amylase from Streptomyces griseus. Usui T, Murata T, Yabuuchi Y, Ogawa K. Carbohydr Res; 1993 Dec 16; 250(1):57-66. PubMed ID: 7511484 [Abstract] [Full Text] [Related]
16. Synthesis of heparin fragments. A chemical synthesis of the pentasaccharide O-(2-deoxy-2-sulfamido-6-O-sulfo-alpha-D-glucopyranosyl)-(1-4 )-O-(beta-D-glucopyranosyluronic acid)-(1-4)-O-(2-deoxy-2-sulfamido-3,6-di-O-sulfo-alpha-D-glu copyranosyl)-(1-4)-O-(2-O-sulfo-alpha-L-idopyranosyluronic acid)-(1-4)-2-deoxy-2-sulfamido-6-O-sulfo-D-glucopyranose decasodium salt, a heparin fragment having high affinity for antithrombin III. Petitou M, Duchaussoy P, Lederman I, Choay J, Sinaÿ P, Jacquinet JC, Torri G. Carbohydr Res; 1986 Mar 15; 147(2):221-36. PubMed ID: 3708627 [Abstract] [Full Text] [Related]
18. Inspection of active sites of human salivary alpha-amylase isozymes by means of non-reducing-end substituted maltooligosaccharides with 2-pyridylamino residue. Omichi K, Ikenaka T. J Biochem; 1986 Apr 15; 99(4):1245-52. PubMed ID: 3486866 [Abstract] [Full Text] [Related]
19. Synthesis of some oligosaccharides containing the O-(2-acetamido-2-deoxy- beta-D-glucopyranosyl)-(1----2)-O-alpha-D-mannopyranosyl unit. Potential substrates for UDP-GlcNAc:alpha-D-mannopyranosyl-(1----6)-N-acetyl-beta-D- glucosaminyltransferase (GnT-V). Khan SH, Abbas SA, Matta KL. Carbohydr Res; 1989 Oct 31; 193():125-39. PubMed ID: 2532953 [Abstract] [Full Text] [Related]
20. Synthesis and utility of sulfated chromogenic carbohydrate model substrates for measuring activities of mucin-desulfating enzymes. Clinch K, Evans GB, Furneaux RH, Rendle PM, Rhodes PL, Roberton AM, Rosendale DI, Tyler PC, Wright DP. Carbohydr Res; 2002 Jun 12; 337(12):1095-111. PubMed ID: 12062525 [Abstract] [Full Text] [Related] Page: [Next] [New Search]