JP2010100583A5 - - Google Patents

Info

Publication number

JP2010100583A5

JP2010100583A5 JP2008274969A JP2008274969A JP2010100583A5 JP 2010100583 A5 JP2010100583 A5 JP 2010100583A5 JP 2008274969 A JP2008274969 A JP 2008274969A JP 2008274969 A JP2008274969 A JP 2008274969A JP 2010100583 A5 JP2010100583 A5 JP 2010100583A5

Authority

JP

Japan

Prior art keywords

branched

glucan

lipid metabolism

triacetylglucitol

trimethyl

Prior art date

2008-10-24

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Withdrawn

Links

• Espacenet
• Global Dossier
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• 229920000310 Alpha glucan Polymers 0.000 claims 6
• 230000037356 lipid metabolism Effects 0.000 claims 6
• 239000003795 chemical substances by application Substances 0.000 claims 5
• 239000000654 additive Substances 0.000 claims 3
• YWIOPJFBNBTWHB-ADOMMUCPSA-N (3r,4s,5r,6s)-4-acetyl-3,4,5,6,7-pentahydroxy-3-(1-hydroxyethyl)-5,6-dimethylnonane-2,8-dione Chemical compound CC(O)[C@](O)(C(C)=O)[C@](O)(C(C)=O)[C@](C)(O)[C@@](C)(O)C(O)C(C)=O YWIOPJFBNBTWHB-ADOMMUCPSA-N 0.000 claims 2
• XWUPIZKXCKBFLR-LANFKUMOSA-N (4r,5s,6r,7s)-4-acetyl-3,4,5,6,7,8-hexahydroxy-5,6,7-trimethyldecane-2,9-dione Chemical compound CC(=O)C(O)[C@](C)(O)[C@@](C)(O)[C@](C)(O)[C@@](O)(C(C)=O)C(O)C(C)=O XWUPIZKXCKBFLR-LANFKUMOSA-N 0.000 claims 2
• 230000000996 additive effect Effects 0.000 claims 2
• 239000003814 drug Substances 0.000 claims 2
• 238000004128 high performance liquid chromatography Methods 0.000 claims 2
• -1 methylated glucitol acetate Chemical class 0.000 claims 2
• XJIAPQKWLOVXHV-SWGNABGMSA-N (3r,4r,5r,6s)-5-acetyl-3,4,5,6,7-pentahydroxy-3-(1-hydroxyethyl)-4,6-dimethylnonane-2,8-dione Chemical compound CC(O)[C@](O)(C(C)=O)[C@@](C)(O)[C@@](O)(C(C)=O)[C@@](C)(O)C(O)C(C)=O XJIAPQKWLOVXHV-SWGNABGMSA-N 0.000 claims 1
• FXFDAYNOUDHHNT-OQMZOEMTSA-N (4r,5r,6r,7s)-4,6-diacetyl-3,4,5,6,7,8-hexahydroxy-5,7-dimethyldecane-2,9-dione Chemical compound CC(=O)C(O)[C@](C)(O)[C@](O)(C(C)=O)[C@](C)(O)[C@@](O)(C(C)=O)C(O)C(C)=O FXFDAYNOUDHHNT-OQMZOEMTSA-N 0.000 claims 1
• SERLAGPUMNYUCK-DCUALPFSSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 claims 1
• 108010001682 Dextranase Proteins 0.000 claims 1
• WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
• AYRXSINWFIIFAE-SCLMCMATSA-N Isomaltose Natural products OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)[C@@H](O)[C@@H](O)[C@@H]1O AYRXSINWFIIFAE-SCLMCMATSA-N 0.000 claims 1
• FXAGBTBXSJBNMD-UHFFFAOYSA-N acetic acid;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound CC(O)=O.OC(=O)CC(O)(C(O)=O)CC(O)=O FXAGBTBXSJBNMD-UHFFFAOYSA-N 0.000 claims 1
• 238000004458 analytical method Methods 0.000 claims 1
• 239000000470 constituent Substances 0.000 claims 1
• 235000013325 dietary fiber Nutrition 0.000 claims 1
• 230000029087 digestion Effects 0.000 claims 1
• 229940079593 drug Drugs 0.000 claims 1
• 239000008103 glucose Substances 0.000 claims 1
• 235000010439 isomalt Nutrition 0.000 claims 1
• 239000000905 isomalt Substances 0.000 claims 1
• HPIGCVXMBGOWTF-UHFFFAOYSA-N isomaltol Natural products CC(=O)C=1OC=CC=1O HPIGCVXMBGOWTF-UHFFFAOYSA-N 0.000 claims 1
• DLRVVLDZNNYCBX-RTPHMHGBSA-N isomaltose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1 DLRVVLDZNNYCBX-RTPHMHGBSA-N 0.000 claims 1
• 239000007788 liquid Substances 0.000 claims 1
• 238000000034 method Methods 0.000 claims 1
• 230000011987 methylation Effects 0.000 claims 1
• 238000007069 methylation reaction Methods 0.000 claims 1
• 238000002156 mixing Methods 0.000 claims 1
• 239000007787 solid Substances 0.000 claims 1