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公开(公告)号:US20240197764A1
公开(公告)日:2024-06-20
申请号:US18504922
申请日:2023-11-08
申请人: NAGAOKA CO., LTD.
IPC分类号: A61K31/7032 , A61K36/61 , A61P3/06
CPC分类号: A61K31/7032 , A61K36/61 , A61P3/06
摘要: A method for inhibiting body fat accumulation comprises a process of taking 3.38 mg or more of oenothein B indicated by the following formula (I) as an effective amount per day.
G in the formula (I) represents a structure of the following formula (II).-
公开(公告)号:US20180332878A1
公开(公告)日:2018-11-22
申请号:US15983762
申请日:2018-05-18
申请人: NAGAOKA CO., LTD.
CPC分类号: A23L27/2024 , A23F3/405 , A23F5/465 , A23G1/32 , A23L2/56 , A23L27/86 , A23V2002/00 , C12G3/06
摘要: A bitter taste inhibitor according to the present disclosure contains isobutyl angelate as an active and a given solvent or a given excipient.
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公开(公告)号:US20180332879A1
公开(公告)日:2018-11-22
申请号:US15983852
申请日:2018-05-18
申请人: NAGAOKA CO., LTD.
发明人: Seiji HASHIMOTO , Kimihiro HIGASHI , Syunsuke YOSHINAGA , Tatsunori TAKIMOTO , Jyunji TOBARI , Nozomu HIRATA , Hirokazu KANENO
摘要: A improving agent for improving aftertaste having high-intensity sweeteners according to the present disclosure contains isobutyl angelate as an active ingredient. A method for improving a sweet taste according to the present disclosure includes adding 0.001 to 1 ppm of isobutyl angelate to an oral composition containing a high-intensity sweetener.
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公开(公告)号:US20140290290A1
公开(公告)日:2014-10-02
申请号:US14301156
申请日:2014-06-10
申请人: NAGAOKA & CO. LTD.
IPC分类号: B01D9/00
CPC分类号: B01D9/0013 , A23L27/203 , B01D9/0036 , C07B2200/07 , C07C29/78 , C07C35/12 , C07C2601/14 , C11B9/022
摘要: Embodiments are provided that provide for efficient production of highly pure natural I-menthol. In some embodiments, a method for preparing natural I-menthol involves providing crude mentha oil in a crystallizer and gradually reducing the temperature of the crystallizer in a step-wise manner, thereby producing highly pure crystals in less than two weeks. The methods disclosed herein are suitable for pharmaceutical GMP.
摘要翻译: 提供了提供高纯度天然I-薄荷醇的有效生产的实施方案。 在一些实施方案中,制备天然I-薄荷醇的方法包括在结晶器中提供粗薄荷油,并逐步地逐渐降低结晶器的温度,从而在不到两周的时间内产生高纯度的晶体。 本文公开的方法适用于药物GMP。
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