会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明授权
    • Cyano-dicarboxylate
    • 氰基二羧酸酯
    • US4521344A
    • 1985-06-04
    • US531095
    • 1983-09-12
    • Jacob S. TouAlfred A. Schleppnik
    • Jacob S. TouAlfred A. Schleppnik
    • C07C51/56C07C57/34C07D307/60
    • C07C57/34C07C51/56
    • A phenylethyl substituted dimer of ethylene and maleic anhydride, named 7-phenyloctane-(1,2),(5,6)-dianhydride, is chemically synthesized by(a) alkylating alkyl 2,4-dihalobutyrate with alkyl 2-cyano-3-phenylbutyrate,(b) alkylating the resulting halide condensation product with a carboxylate selected from the group consisting of trialkyl ethane-1,1,2-tricarboxylate and dimethyl cyanoethane-1,2-dicarboxylate,(c) acid hydrolyzing the resulting tetra or pentaester accompanied by decarboxylating, and(d) dehydrating the resulting tetra-acid to yield the desired phenylethyl substituted dimer of ethylene and maleic anhydride,wherein the alkyls in the butyrate and carboxylate ester groups each contain from one to about four carbon atoms and halo is selected from the group consisting of bromo, chloro and iodo.
    • 乙烯和马来酸酐的苯基乙基取代二聚体,命名为7-苯辛基 - (1,2),(5,6) - 二氢化钠,是通过(a)使2,4-二卤代烷基烷基化与2-氰基-3- - 苯基丁酸酯,(b)将所得的卤化物缩合产物与选自三烷基乙烷-1,1,2-三羧酸三乙酯和二甲基氰基乙烷-1,2-二羧酸酯的羧酸烷基化,(c)酸水解所得四 五酸酯伴随着脱羧,和(d)使得到的四酸脱水得到乙烯和马来酸酐所需的苯基乙基取代的二聚体,其中丁酸酯和羧酸酯基团中的烷基各自含有1个至约4个碳原子,卤素是 选自溴,氯和碘。
    • 3. 发明授权
    • Cyano-polycarboxylates
    • 氰基 - 多羧酸盐
    • US4514340A
    • 1985-04-30
    • US531104
    • 1983-09-12
    • Jacob S. TouAlfred A. Schleppnik
    • Jacob S. TouAlfred A. Schleppnik
    • C07C51/56C07C57/34C07C121/66
    • C07C57/34C07C51/56
    • A phenylethyl substituted dimer of ethylene and maleic anhydride, named 7-phenyloctane-(1,2),(5,6)-dianhydride, is chemically synthesized by(a) alkylating alkyl 2,4-dihalobutyrate with alkyl 2-cyano-3-phenylbutyrate,(b) alkylating the resulting halide condensation product with a carboxylate selected from the group consisting of trialkyl ethane-1,1,2-tricarboxylate and dimethyl cyanoethane-1,2-dicarboxylate,(c) acid hydrolyzing the resulting tetra or pentaester accompanied by decarboxylating, and(d) dehydrating the resulting tetra-acid to yield the desired phenylethyl substituted dimer of ethylene and maleic anhydride,wherein the alkyls in the butyrate and carboxylate ester groups each contain from one to about four carbon atoms and halo is selected from the group consisting of bromo, chloro and iodo.
    • 乙烯和马来酸酐的苯基乙基取代二聚体,命名为7-苯辛基 - (1,2),(5,6) - 二氢化钠,是通过(a)使2,4-二卤代烷基烷基化与2-氰基-3- - 苯基丁酸酯,(b)将所得的卤化物缩合产物与选自三烷基乙烷-1,1,2-三羧酸三乙酯和二甲基氰基乙烷-1,2-二羧酸酯的羧酸烷基化,(c)酸水解所得四 五酸酯伴随着脱羧,和(d)使得到的四酸脱水得到乙烯和马来酸酐所需的苯基乙基取代的二聚体,其中丁酸酯和羧酸酯基团中的烷基各自含有1个至约4个碳原子,卤素是 选自溴,氯和碘。
    • 4. 发明授权
    • Chemical synthesis of ethylene/maleic anhydride dimer with phenylethyl
end group
    • 乙烯/马来酸酐二聚体与苯基乙基端基的化学合成
    • US4442298A
    • 1984-04-10
    • US413009
    • 1982-08-30
    • Jacob S. TouAlfred A. Schleppnik
    • Jacob S. TouAlfred A. Schleppnik
    • C07C51/56C07C57/34C07D307/60
    • C07C57/34C07C51/56
    • A phenylethyl substituted dimer of ethylene and maleic anhydride, names 7-phenyloctane-(1,2),(5,6)-dianhydride, is chemically synthesized by(a) alkylating alkyl 2,4-dihalobutyrate with alkyl 2-cyano-3-phenylbutyrate,(b) alkylating the resulting halide condensation product with a carboxylate selected from the group consisting of trialkyl ethane-1,1,2-tricarboxylate and dimethyl cyanoethane-1,2-dicarboxylate,(c) acid hydrolyzing the resulting tetra or pentaester accompanied by decarboxylating, and(d) dehydrating the resulting tetra-acid to yield the desired phenylethyl substituted dimer of ethylene and maleic anhydride,wherein the alkyls in the butyrate and carboxylate ester groups each contain from one to about four carbon atoms and halo is selected from the group consisting of bromo, chloro and iodo.The dimer has anti-tumor and anti-viral properties and can be used in silver halide emulsions.
    • 乙烯和马来酸酐的苯基乙基取代的二聚体名称为7-苯辛基 - (1,2),(5,6) - 二氢化物,是通过(a)使2,4-二卤代烷基烷基化与2-氰基-3- - 苯基丁酸酯,(b)将所得的卤化物缩合产物与选自三烷基乙烷-1,1,2-三羧酸三乙酯和二甲基氰基乙烷-1,2-二羧酸酯的羧酸烷基化,(c)酸水解所得四 五酸酯伴随着脱羧,和(d)使得到的四酸脱水得到乙烯和马来酸酐所需的苯基乙基取代的二聚体,其中丁酸酯和羧酸酯基团中的烷基各自含有1个至约4个碳原子,而卤素是 选自溴,氯和碘。 二聚体具有抗肿瘤和抗病毒性质,可用于卤化银乳剂。
    • 5. 发明授权
    • Method of removing n-terminal alanine residues from polypeptides with aeromonas aminopeptidase
    • 从氨基肽酶气单胞菌多肽中除去N-末端丙氨酸残基的方法
    • US06794159B1
    • 2004-09-21
    • US09541844
    • 2000-04-03
    • Jacob S. TouDouglas W. Taylor
    • Jacob S. TouDouglas W. Taylor
    • C12P2106
    • C12N9/48C07K14/61
    • This invention describes a method of removing N-terminal alanine residues from polypeptides, preferably recombinant proteins, using an aminopeptidase derived from the marine bacterium Aeromonas proteolytica. Accordingly, Aeromonas aminopeptidase (AAP; E.C. 3.4.11.10) can be used to remove N-terminal alanyl residues from derivatives of human somatotropin (hST, human growth hormone, or hGH), porcine somatotropin (pST), and bovine somatotropin (bST), for example, to yield proteins having their native amino acid sequences. The enzyme reactions can be carried out in free solution, or the AAP can be immobilized on a solid support, for reactions carried out in vitro. An efficient method for converting Ala-hGH to hGH, for example, comprises expression of Ala-hGH in E. coli, recovery of inclusion bodies, solubilization and refolding in detergent, detergent removal by ultrafiltration, selective precipitation, enzyme cleavage, followed by two column chromatography steps.
    • 本发明描述了使用衍生自海洋细菌嗜水气单胞菌的氨基肽酶从多肽,优选重组蛋白中除去N-末端丙氨酸残基的方法。 因此,气单胞菌氨基肽酶(AAP; EC 3.4.11.10)可用于从人类生长激素(hST,人生长激素或hGH),猪生长激素(pST)和牛生长激素(bST)的衍生物中除去N-末端丙氨酰残基, 例如,产生具有其天然氨基酸序列的蛋白质。 酶反应可以在游离溶液中进行,或者AAP可以固定在固体支持物上,用于在体外进行的反应。 例如,将Ala-hGH转化为hGH的有效方法包括在大肠杆菌中表达Ala-hGH,回收包涵体,在洗涤剂中溶解和重折叠,通过超滤去除洗涤剂,选择性沉淀,酶切,然后是两个 柱色谱步骤。
    • 7. 发明授权
    • Method of removing N-terminal alanine residues from polypeptides with Aeromonas aminopeptidase
    • 用气单胞菌氨肽酶从多肽中除去N-末端丙氨酸残基的方法
    • US06743600B1
    • 2004-06-01
    • US10018304
    • 2002-09-16
    • Jacob S. TouDouglas W. Taylor
    • Jacob S. TouDouglas W. Taylor
    • C12Q137
    • C12P21/06C07K14/61
    • This invention describes a method of removing N-terminal alanine residues from polypeptides, preferably recombinant proteins, using an aminopeptidase derived from the marine bacterium Aeromonas proteolytica. Accordingly, Aeromonas aminopeptidase (AAP; E.C. 3.4.11.10) can be used to remove N-terminal alanyl residues from derivatives of human somatotropin (hST, human growth hormone, or hGH), porcine somatotropin (pST), and bovine somtotropin (bST), for example, to yield proteins having their native amino acid sequences. The enzyme reactions can be carried out in free solution, or the AAP can be immobilized on a solid support, for reactions carried out in vitro. An efficient method for converting Ala-hGH to hGH, for example, comprises expression of Ala-hGH in E. coli, recovery of inclusion bodies, solubilization and refolding in detergent, detergent removal by ultrafiltration, selective precipitation, enzyme cleavage, followed by two column chromatography steps.
    • 本发明描述了使用衍生自海洋细菌嗜水气单胞菌的氨基肽酶从多肽,优选重组蛋白中除去N-末端丙氨酸残基的方法。 因此,气单胞菌氨基肽酶(AAP; EC 3.4.11.10)可用于从人类生长激素(hST,人生长激素或hGH),猪生长激素(pST)和牛嗜马逊托品(bST)的衍生物中除去N-末端丙氨酰残基, 例如,产生具有其天然氨基酸序列的蛋白质。 酶反应可以在游离溶液中进行,或者AAP可以固定在固体支持物上,用于在体外进行的反应。 例如,将Ala-hGH转化为hGH的有效方法包括在大肠杆菌中表达Ala-hGH,回收包涵体,在洗涤剂中溶解和重折叠,通过超滤去除洗涤剂,选择性沉淀,酶切,然后是两个 柱色谱步骤。