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公开(公告)号：US20110014141A1
公开(公告)日：2011-01-20
申请号：US12819807
申请日：2010-06-21
CPC分类号： A61Q19/02 , A61K8/0208 , A61K8/19 , A61K8/347 , A61K8/35 , A61K8/362 , A61K8/365 , A61K8/368 , A61K8/41 , A61K8/44 , A61K8/466 , A61K8/4926 , A61K8/494 , A61K8/4946 , A61K8/498 , A61K8/4986 , A61K8/60 , A61K8/602 , A61K8/64 , A61K8/671 , A61K8/673 , A61K8/676 , A61K8/678 , A61K8/68 , A61K8/735 , A61K8/736 , A61K8/86 , A61K8/97 , A61K8/9706 , A61K8/982 , A61K36/06 , A61K36/23 , A61K36/258 , A61K36/484 , A61K36/515 , A61Q19/00 , A61K2300/00
摘要： The objective of the present invention was to enhance the skin whitening effects and blackening prevention effects and supply safe and stable topical agents for dermatological use. For that purpose 4-Hydroxyphenyl-α-D-glucopyranoside was combined with auxiliary agents such as ascorbic acid and its derivatives, crude drugs and its extracts, hydroxycarboxylic acid and its salts, oil soluble glycyrrhiza extract, gentian extract, phenol derivatives and their salts, placenta extract, kojic acid and its derivatives, glucosamine and its derivatives, azelaic acid and its derivatives, retinol and its derivatives, pyridoxin and its derivatives, tocopherol and its derivatives, chitosan and its decomposition products, caffeic acid derivatives, hydroxycinnamate and its derivatives, Umbelliferae plant extracts, mycelial cultures and their extracts, plant leaves and their extracts.
摘要翻译： 本发明的目的是增强皮肤美白效果和防止黑化作用，并提供用于皮肤病学用途的安全和稳定的外用剂。 为此目的，将4-羟基苯基-α-D-吡喃葡萄糖苷与助剂如抗坏血酸及其衍生物，生药及其提取物，羟基羧酸及其盐，油溶性甘草提取物，龙胆提取物，苯酚衍生物及其盐 ，胎盘提取物，曲酸及其衍生物，葡糖胺及其衍生物，壬二酸及其衍生物，视黄醇及其衍生物，吡哆酮及其衍生物，生育酚及其衍生物，壳聚糖及其分解产物，咖啡酸衍生物，羟基肉桂酸酯及其衍生物 ，伞形植物提取物，菌丝体培养物及其提取物，植物叶及其提取物。
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公开(公告)号：US07033800B2
公开(公告)日：2006-04-25
申请号：US10240057
申请日：2001-03-28
CPC分类号： C12P19/44 , C12P19/445
摘要： A method of producing a phenol derivative glycoside is provided. The method comprises the step of allowing a saccharide and a phenol derivative to react with each other in the presence of an enzyme to produce the phenol derivative glycoside. The enzyme is selected from the group consisting of neopullulanase, cyclomaltodextrinase, maltogenic α-amylase, and saccharifying amylase having cyclodextrin synthesizing capability.
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公开(公告)号：US09376467B2
公开(公告)日：2016-06-28
申请号：US14004058
申请日：2012-02-28
申请人： Yusuke Kono , Shuji Fujita , Hideaki Suzuki , Mari Okumoto , Takashi Nakae , Kazuhiro Chiba
发明人： Yusuke Kono , Shuji Fujita , Hideaki Suzuki , Mari Okumoto , Takashi Nakae , Kazuhiro Chiba
摘要： The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.
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4.发明申请NOVEL CROSS-LINKED PEPTIDES CONTAINING NON-PEPTIDE CROSS-LINKED STRUCTURE, METHOD FOR SYNTHESIZING CROSS-LINKED PEPTIDES, AND NOVEL ORGANIC COMPOUND USED IN METHOD 有权含有非肽交联结构的新型交联肽，合成交联肽的方法和方法中使用的新型有机化合物公开(公告)号：US20130345393A1
公开(公告)日：2013-12-26
申请号：US14004058
申请日：2012-02-28
申请人： Yusuke Kono , Shuji Fujita , Hideaki Suzuki , Mari Okumoto , Takashi Nakae , Kazuhiro Chiba
发明人： Yusuke Kono , Shuji Fujita , Hideaki Suzuki , Mari Okumoto , Takashi Nakae , Kazuhiro Chiba
摘要： The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.
摘要翻译： 本发明的目的是提供一种含有新型非肽交联结构的交联肽及其合成方法。 提供具有新型非肽交联结构的交联肽，用于合成交联肽的有用中间体，以及合成新型交联肽和中间体的方法。 交联肽的特征在于在交联结构中具有-NR-键。 通过使用交联肽的合成方法，可以自由地设计交联，可以自由地进行交联。
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公开(公告)号：US20230019988A1
公开(公告)日：2023-01-19
申请号：US17782330
申请日：2020-12-04
申请人： Takashi NAKAE , Paul KAPPOCK , Yoshiyuki IWASE , Josef SCHROER , Jurgen RIEGLER , Peter VAN AKEN , ARXADA AG
发明人： Takashi Nakae , Paul Kappock , Yoshiyuki Iwase , Josef Schroeer , Jurgen Riegler , Peter Van Aken
IPC分类号： C09D133/08 , C09D7/61 , C09D5/14 , C09D5/16
摘要： The present invention relates to antifouling compositions comprising compounds of formula IA and/or IB that are highly effective against marine biofouling of surfaces of ships and marine structures, their use for inhibiting marine biofouling, as well as antifouling paints comprising said compositions.
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