CRYSTALLINE CARBOHYDRATE DERIVATIVE
    24.
    发明申请
    CRYSTALLINE CARBOHYDRATE DERIVATIVE 有权
    碳水化合物衍生物

    公开(公告)号:US20110166339A1

    公开(公告)日:2011-07-07

    申请号:US13054314

    申请日:2009-07-15

    IPC分类号: C07H5/06

    CPC分类号: C07H5/06 C07H1/00

    摘要: α-Lactosamine hydrochloride, substantially free of β-lactosamine hydrochloride; a method of preparing α-lactosamine hydrochloride monohydrate from an anomeric mixture of lactosamine hydrochloride, including: preparing a solution including the anomeric mixture of lactosamine hydrochloride, water and at least one water-miscible organic solvent at a temperature of 0-100° C., and cooling the solution to cause crystallisation of α-lactosamine hydrochloride monohydrate; a method of preparing anhydrous α-lactosamine hydrochloride; and use of α-lactosamine hydrochloride as a food supplement or intermediate in synthesis.

    摘要翻译: α-乳糖胺盐酸盐,基本上不含β-乳糖胺盐酸盐; 一种从乳糖胺盐酸盐的端基异构体混合物制备α-乳糖胺盐酸盐一水合物的方法,包括:在0-100℃的温度下制备包括乳糖胺盐酸盐,水和至少一种水混溶性有机溶剂的端基异构体混合物的溶液 ,并冷却该溶液以引起α-乳糖胺盐酸盐一水合物的结晶; 制备无水α-乳糖胺盐酸盐的方法; 并使用盐酸α-乳糖胺作为食品添加剂或中间体。

    MIXTURE OF HMOs
    28.
    发明申请

    公开(公告)号:US20230000886A1

    公开(公告)日:2023-01-05

    申请号:US17780869

    申请日:2020-11-27

    申请人: Glycom A/S

    IPC分类号: A61K31/702 A61P1/12

    摘要: The invention relates to a human milk oligosaccharide (HMO) for use in, a synthetic composition comprising an HMO for use in, and a method for prophylactically reducing gastrointestinal IBS symptom severity and/or symptom occurrence in a lac-tose-intolerant, IBS patient; reintroducing a source of lactose into the diet of a lactose-intolerant, IBS patient while prophylactically reducing gastrointestinal IBS symptom severity and/or symptom occurrence in the IBS patient; and/or reducing the severity and/or occurrence of non-gastrointestinal symptoms in a lactose-intolerant, IBS patient.

    Synthetic composition for treating metabolic disorders

    公开(公告)号:US11529364B2

    公开(公告)日:2022-12-20

    申请号:US17093337

    申请日:2020-11-09

    申请人: GLYCOM A/S

    摘要: A method for treating metabolic disorders in non-infant includes administering to an obese non-infant human during a treatment period an effective amount of a mixture of two or more synthetic neutral human milk oligosaccharides (HMOs) selected from 2′-fucosyllactose (2′FL), 3-fucosyllactose (3-FL), difucosyllactose (DFL), lacto-N-fucopentaose I (LNFP-I), lacto-N-tetraose (LNT), and lacto-N-neotetraose (LNnT), and optionally one or more excipients. The method further includes increasing in the gastrointestinal microbiota of the non-infant human during the treatment period, the relative abundance of Bifidobacterium adolescentis and reducing in the non-infant human during the treatment period, a precursor condition for a metabolic disorder associated with development of one or more of obesity-induced pre-diabetes and type 2 diabetes, the precursor condition selected from gut permeability, metabolic endotoxemia, low-grade metabolic inflammation, and body fat percentage.