-
1.发明授权Multipurpose method for constructing an error-control code for multilevel memory cells operating with a variable number of storage levels, and multipurpose error-control method using said error-control code 失效用于构建以可变数量的存储级别操作的多级存储器单元的错误控制代码的多用途方法，以及使用所述错误控制代码的多用途错误控制方法公开(公告)号：US07047478B2
公开(公告)日：2006-05-16
申请号：US10015949
申请日：2001-11-02
申请人： Stefano Gregori , Pietro Ferrari , Guido Torelli
发明人： Stefano Gregori , Pietro Ferrari , Guido Torelli
CPC分类号： H03M13/00 , G11C2211/5641
摘要： Described is an error control method for multilevel memory cells operating with a variable number of storage levels. The method includes: receiving a first information word having k input symbols each in a first base; converting the first information word into a second base by converting the input symbols into input symbols in the second base; encoding the converted first information word into a first codeword having k+n coded symbols in the second base; and writing the first codeword into the multilevel memory cells. The encoding step may include generating a generating matrix and multiplying the first information word by the generating matrix to produce the first codeword.
摘要翻译： 描述了对具有可变数量的存储级别操作的多级存储器单元的错误控制方法。 该方法包括：在第一基站中接收具有k个输入符号的第一信息字; 通过将输入符号转换为第二基底中的输入符号将第一信息字转换成第二基底; 将转换的第一信息字编码为在第二基底中具有k + n个编码符号的第一码字; 以及将所述第一码字写入所述多层存储器单元。 编码步骤可以包括生成生成矩阵并将第一信息字乘以生成矩阵以产生第一码字。
-
2.发明授权
公开(公告)号：US5164484A
公开(公告)日：1992-11-17
申请号：US778764
申请日：1991-10-21
申请人： Adriano Malabarba , Pietro Ferrari , Aldo Trani , Giorgio Tarzia
发明人： Adriano Malabarba , Pietro Ferrari , Aldo Trani , Giorgio Tarzia
IPC分类号： C07K9/00
CPC分类号： C07K9/008 , Y10S930/19 , Y10S930/27
摘要： The present invention is directed to new de-(acetylglucosaminyl)-di(dehydro)deoxy teicoplanin derivatives which possess antibiotic activity mainly against gram positive bacteria.The new compounds are obtained by chemical modification of a teicoplanin antibiotic substance.
摘要翻译： 本发明涉及具有主要抗革兰氏阳性细菌的抗生素活性的新的脱（乙酰葡糖胺基） - 二（脱氢）脱氧替考拉宁衍生物。 新化合物通过替考拉宁抗生素物质的化学修饰获得。
-
公开(公告)号：US5854036A
公开(公告)日：1998-12-29
申请号：US716259
申请日：1996-09-10
IPC分类号： C12Q1/42 , A61K31/34 , A61K35/74 , A61P25/24 , A61P25/26 , C07D307/94 , C07G99/00 , C12P17/04 , C12R1/645
CPC分类号： C07D307/94 , C12P17/04
摘要： The present invention concerns novel compounds obtained by fermenting a microorganism of the genus Memnonoiella or Stachybotrys, which compounds are inhibitors of the enzyme inositol monophosphatase (EC 3.1.3.25). The present invention also relates to the use of these novel compounds in treating manic depression and pharmaceutical formulations comprising said compounds as active ingredient; a further object is the use of these compounds in an analytical method for detecting inositol monophosphatase.
摘要翻译： PCT No.PCT / EP95 / 01045 Sec。 371日期：1996年9月10日 102（e）1996年9月10日PCT 1995年3月21日PCT PCT。 公开号WO95 / 26344 日期1995年10月5日本发明涉及通过发酵Memnonoiella或Stachybotrys的微生物获得的新型化合物，该化合物是肌醇单磷酸酶的抑制剂（EC 3.1.3.25）。 本发明还涉及这些新化合物在治疗躁狂抑郁症中的用途以及包含所述化合物作为活性成分的药物制剂; 另一个目的是在检测肌醇单磷酸酶的分析方法中使用这些化合物。
-
公开(公告)号：US5843890A
公开(公告)日：1998-12-01
申请号：US462997
申请日：1995-06-05
IPC分类号： A61K31/44 , A61K38/00 , A61P3/00 , A61P31/00 , C07D513/22 , C07K5/078 , C12P17/18 , C12P21/04 , C12R1/01 , A61K35/70
CPC分类号： C07K5/06139 , A61K38/00
摘要： The present invention is directed to new antibiotic substances denominated antibiotic GE 2270 factors B.sub.1, B.sub.2, C.sub.1, C.sub.2, D.sub.1, D.sub.2, E and T, the addition salts thereof, the pharmaceutical compositions thereof and their use as medicaments, particularly in the treatment of infectious diseases involving microorganisms susceptible to them and their use as animal growth promoters.
-
5.发明授权O.sup.56 -alkyl derivatives of aglycone and pseudo aglycones of teicoplanin 失效糖精苷的O-末端烷基衍生物和替考拉宁的假糖基苷
公开(公告)号：US5185320A
公开(公告)日：1993-02-09
申请号：US707247
申请日：1991-05-22
申请人： Aldo Trani , Pierfausto Seneci , Pietro Ferrari , Romeo Ciabatti
发明人： Aldo Trani , Pierfausto Seneci , Pietro Ferrari , Romeo Ciabatti
IPC分类号： C07K9/00
CPC分类号： C07K9/008
摘要： The present invention is directed to a new class of teicoiplanin derivatives, a process for preparing them and their use as pharmaceutically active substances.
摘要翻译： 本发明涉及一类新的替米卡因衍生物，其制备方法及其作为药物活性物质的用途。
-
公开(公告)号：US4908351A
公开(公告)日：1990-03-13
申请号：US304421
申请日：1989-01-24
IPC分类号： C12P21/02 , A61K38/00 , A61P31/04 , C07H17/00 , C07K1/02 , C07K1/113 , C07K1/22 , C07K9/00 , C07K14/195 , C07K14/41 , A61K37/02 , C07K5/12
CPC分类号： C07K9/008
摘要： The present invention is directed to a new antibiotic substance denominated antibiotic A 42867 pseudoaglycon, a pharmaceutically acceptable salt thereof, a process for its preparation from antibiotic A 42867 and pharmaceutical compositions containing the new substance of the invention.
-
7.发明授权Antibiotic GE 2270 factors B.sub.1, B.sub.2, C.sub.1, C.sub.2, D.sub.1, D.sub.2, E and T 失效抗生素GE 2270因子B1，B2，C1，C2，D1，D2，E和T
公开(公告)号：US5747295A
公开(公告)日：1998-05-05
申请号：US460177
申请日：1995-06-02
IPC分类号： A61K31/44 , A61K38/00 , A61P3/00 , A61P31/00 , C07D513/22 , C07K5/078 , C12P17/18 , C12P21/04 , C12R1/01 , C12P1/00
CPC分类号： C07K5/06139 , A61K38/00
摘要： The present invention is directed to new antibiotic substances denominated antibiotic GE 2270 factors B.sub.1, B.sub.2, C.sub.1, C.sub.2, D.sub.1, D.sub.2, E and T, the addition salts thereof, the pharmaceutical compositions thereof and their use as medicaments, particularly in the treatment of infectious diseases involving microorganisms susceptible to them and their use as animal growth promoters.
摘要翻译： 本发明涉及新型抗生素物质GE 2270因子B1，B2，C1，C2，D1，D2，E和T，其加成盐，其药物组合物及其作为药物的用途，特别是用于治疗 涉及对它们敏感的微生物的感染性疾病及其作为动物生长促进剂的用途。
-
8.发明授权
公开(公告)号：US4789661A
公开(公告)日：1988-12-06
申请号：US102198
申请日：1987-07-17
申请人： Adriano Malabarba , Aldo Trani , Pietro Ferrari , Giorgio Tarzia
发明人： Adriano Malabarba , Aldo Trani , Pietro Ferrari , Giorgio Tarzia
CPC分类号： C07K9/008 , Y10S930/19 , Y10S930/27
摘要： The present invention is directed to new de-(acetylglucosaminyl-di(dehydro)deoxy teicoplanin derivatives which possess antibiotic activity mainly against gram positive bacteria.The new compounds are obtained by chemical modification of a teicoplanin antibiotic substance.
摘要翻译： 本发明涉及具有主要抗革兰氏阳性菌的抗生素活性的新的脱（乙酰葡糖胺基 - 二（脱氢）脱氧替考拉宁衍生物），新化合物是通过化学改性替考拉宁抗生素物质获得的。
-
公开(公告)号：US4782042A
公开(公告)日：1988-11-01
申请号：US945732
申请日：1986-12-23
IPC分类号： C12P21/00 , A61K35/74 , A61K38/00 , A61P31/04 , C07K1/113 , C07K1/12 , C07K7/06 , C07K7/64 , C07K9/00 , C12P21/02 , C12R1/03 , A61K37/02 , C07K5/12
CPC分类号： C07K9/008 , Y10S930/19 , Y10S930/27
摘要： The present invention concerns a new antibiotic substance denominated antibiotic A 40926 mannosyl aglycon and the addition salts thereof, a process for preparing it from antibiotic A 40926 complex or a factor thereof, and its use in the treatment of infectious disease involving microorganisms susceptible to it.
摘要翻译： 本发明涉及一种新型的抗生素物质A40926甘露糖基糖苷配基及其加成盐，其由抗生素A40926复合物或其因子制备的方法及其用于治疗涉及对其敏感的微生物的感染性疾病。
-
10.发明授权Water-soluble alkanoyloxy and alkoxycarbonyloxy rifampicin derivatives, process for its preparation, intermediates, and its pharmaceutical composition as antibacterials 失效水溶性烷酰氧基和烷氧基羰氧基利福平衍生物，其制备方法，中间体及其作为抗菌剂的药物组合物
公开(公告)号：US4585589A
公开(公告)日：1986-04-29
申请号：US626358
申请日：1984-06-29
IPC分类号： A61K31/495 , A61P31/04 , C07D498/08
CPC分类号： C07D498/08
摘要： The present invention is directed to new water soluble rifampicin derivatives which are suitable for preparing aqueous solutions for oral or parenteral administration. The new derivatives of the invention are 4 and/or 8 alkanoyl or alkanoyloxyalkyl esters of rifampicin and possess essentially the same antibacterial activity of this widely known antibiotic substance.
摘要翻译： 本发明涉及适用于制备用于口服或肠胃外给药的水溶液的新的水溶性利福平衍生物。 本发明的新衍生物是利福平的4种和/或8种烷酰基或烷酰氧基烷基酯，并且具有与该广为人知的抗生素物质基本相同的抗菌活性。
-
-
-
-
-
-
-
-
-
搜索结果
11 条记录 (耗时 0.025 秒)
