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1. 发明申请

US20050080015A1 Carboline-3-carboxylic acid modified related sequences of Ala-Arg-Pro-Ala-Lys, their synthesis and use as thromobolytic agent 有权
标题翻译：羧酸修饰的Ala-Arg-Pro-Ala-Lys相关序列，它们的合成和用作溶血剂
公开(公告)号：US20050080015A1
公开(公告)日：2005-04-14
申请号：US10680293
申请日：2003-10-08
申请人： Shiqi Peng , Ming Zhao , Chao Wang , Yangfen Wu
发明人： Shiqi Peng , Ming Zhao , Chao Wang , Yangfen Wu
IPC分类号： A61K38/00 , C07K14/75 , A61K38/08 , C07K7/06
CPC分类号： C07K14/75 , A61K38/00
摘要： The present invention relates to the protected intermediates and the deprotected products of P6A, related to the protected pseudopeptides introducing the protected intermediateds of P6A to 3S-(2-Boc)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid and the deprotected pseudopeptides, related to the protected pseudopeptides introducing the protected intermediateds of P6A to 3S-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid benzyl ester, related to the methods for their preparation, and related to their use as the thrombolytic agents.
摘要翻译：本发明涉及受保护的中间体和P6A的去保护产物，其与被保护的假肽相关，引入受保护的中间体P6A至3S-（2-Boc）-1,2,3,4-四氢-β-咔啉-3 羧酸和去保护的假肽，与保护的假肽相关，引入受保护的中间体P6A至3S-1,2,3,4-四氢-β-咔啉-3-羧酸苄酯，涉及其制备方法，并且与它们作为溶栓剂的用途有关。

2. 发明授权

US07138491B2 Carboline-3-carboxylic acid modified related sequences of Ala-Arg-Pro-Ala-Lys, their synthesis and use as thromobolytic agent 有权
标题翻译：羧酸修饰的Ala-Arg-Pro-Ala-Lys相关序列，它们的合成和用作溶血剂
公开(公告)号：US07138491B2
公开(公告)日：2006-11-21
申请号：US10680293
申请日：2003-10-08
申请人： Shiqi Peng , Ming Zhao , Chao Wang , Yangfen Wu
发明人： Shiqi Peng , Ming Zhao , Chao Wang , Yangfen Wu
IPC分类号： A61K38/00
CPC分类号： C07K14/75 , A61K38/00
摘要： The present invention relates to the protected intermediates and the deprotected products of P6A, related to the protected pseudopeptides introducing the protected intermediateds of P6A to 3S-(2-Boc)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid and the deprotected pseudopeptides, related to the protected pseudopeptides introducing the protected intermediateds of P6A to 3S-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid benzyl ester, related to the methods for their preparation, and related to their use as the thrombolytic agents.
摘要翻译：本发明涉及受保护的中间体和P6A的去保护产物，其与被保护的假肽相关，引入受保护的中间体P6A至3S-（2-Boc）-1,2,3,4-四氢-β-咔啉-3 羧酸和去保护的假肽，与保护的假肽相关，引入受保护的中间体P6A至3S-1,2,3,4-四氢-β-咔啉-3-羧酸苄酯，涉及其制备方法，并且与它们作为溶栓剂的用途有关。

3. 发明申请

US20050043396A1 5-Benzoylamino-1,3-dioxacyclanes, the method for preparing the same and their use as PKC inhibitor 审中-公开
标题翻译： 5-苯甲酰氨基-1,3-二氧环己烷，其制备方法及其作为PKC抑制剂的用途
公开(公告)号：US20050043396A1
公开(公告)日：2005-02-24
申请号：US10674148
申请日：2003-09-29
申请人： Hayley Zen , Shiqi Peng , Lanrong Bi , Ming Zhao , Chao Wang
发明人： Hayley Zen , Shiqi Peng , Lanrong Bi , Ming Zhao , Chao Wang
IPC分类号： C07D273/06 , C07D319/06 , C07D321/12 , A61K31/335
CPC分类号： C07D319/06 , C07D273/06 , C07D321/12
摘要： The present invention discloses a series of benzoylamino-1,3-dioxacyclane compounds, of which compounds 1-21 were prepared via transacetalisation reaction between N-benzoylaminoglycol and 1,1,3,3-tetramethoxypropane; while compounds 22-48 were prepared via stereospecific acetalisation reaction between N-benzoylamino glycol and aromatic aldehyde, and if necessary, the nitro groups were reduced and further be salified with propane diacid and L-Arg or L-Lys. These compounds possess the structural type of PKC inhibitor and positive anti-inflammatory effect, and can be applied in medical fields as PKC inhibitor for corresponding therapy.
摘要翻译：本发明公开了一系列苯甲酰基氨基-1,3-二氧杂环烷化合物，其中化合物1-21是通过N-苯甲酰氨基甘氨酸与1,1,3,3-四甲氧基丙烷之间的转化反应制备的; 而化合物22-48通过N-苯甲酰氨基二醇和芳族醛之间的立体特异性缩醛化反应制备，并且如果需要，硝基还原，并进一步用丙烷二酸和L-Arg或L-Lys进行成盐。这些化合物具有PKC抑制剂的结构型和阳性消炎作用，可作为PKC抑制剂用于医学领域，用于相应的治疗。

4. 发明授权

US06306837B1 Heavy metal chelating agent for oral administration, its synthesis and its uses in medicine and health protection 有权
标题翻译：一种用于口服给药的新型重金属螯合剂，其合成及其在医药和保健中的应用
公开(公告)号：US06306837B1
公开(公告)日：2001-10-23
申请号：US09473737
申请日：1999-12-28
申请人： Shiqi Peng , Chao Wang , Ming Zhao , Xingwei Li , Yancheng Wu , Taigang Mo
发明人： Shiqi Peng , Chao Wang , Ming Zhao , Xingwei Li , Yancheng Wu , Taigang Mo
IPC分类号： A61K3170
CPC分类号： C07H15/12 , Y10S514/836
摘要： The present invention relates to a new kind of heavy metal chelating agents and a preparation process and uses thereof. The said heavy metal chelating agents are expressed in &agr;-[D(+)glucose-1-yl-amino]-&bgr;3-mercapto-(S)-propanoic acid (abbreviated to NGP,I) and/or N,N′-di[D(+)glucose-1-yl]-L-cystine (abbreviated to NGCD,II). In the process of preparation, glucose and cysteine are reacted with a base, with a reducing agent, and the obtained products are acidified to give NGP,I, which can be used in and/or as drugs, health foods and food additives for accelerating the excretion of heavy metals including Pb, Cd, Hg, Al, Sb, As, etc. The structural feature of the compounds of the present invention is that they contain glucose and cysteirie in their molecules. Compared with the heavy metal-excreting drugs of prior art, the compounds of the present invention have four advantages, namely suitability for oral administration, high ability to accelerate the excretion of heavy metals, high selectivity and less toxicity.
摘要翻译：本发明涉及一种新型的重金属螯合剂及其制备方法和用途。所述重金属螯合剂在α-[D（+）葡萄糖-1-基 - 氨基]-β-巯基 - （S） - 丙酸（缩写为NGP，I）和/或N，二[D（+）葡萄糖-1-基] -L-胱氨酸（缩写为NGCD，II）。在制备过程中，葡萄糖和半胱氨酸与碱反应，还原剂，将所得产物酸化，得到NGP，I，可用于和/或作为药物的保健食品和食品添加剂加速重金属的排泄，包括Pb，Cd，Hg，Al，Sb，As等。本发明化合物的结构特征是它们在其分子中含有葡萄糖和半胱氨酸。与现有技术的重金属排泄物相比，本发明的化合物具有四个优点，即口服适用性，加速重金属排泄能力高，选择性低，毒性小。

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