-
公开(公告)号：US3974140A
公开(公告)日：1976-08-10
申请号：US604480
申请日：1975-08-13
IPC分类号： A61K31/43 , C07C275/60 , C07D499/64 , C07D499/68 , C07D499/70
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D499/68
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
摘要翻译： 6-（α-3-酰基 - 脲基乙酰胺基） - 青霉烷酸及其药学上可接受的无毒盐，其中存在于3-位的氮原子的氢原子被取代，对革兰氏阳性和革兰氏阴性有效 感染，特别是克雷伯杆菌感染。
-
公开(公告)号：US3936442A
公开(公告)日：1976-02-03
申请号：US426308
申请日：1973-12-19
IPC分类号： A61K31/43 , C07C275/60 , C07D499/64 , C07D499/58
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D499/68
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
摘要翻译： 6-（α-3-酰基 - 脲基乙酰胺基） - 青霉烷酸及其药学上可接受的无毒盐，其中存在于3-位的氮原子的氢原子被取代，对革兰氏阳性和革兰氏阴性有效 感染，特别是克雷伯杆菌感染。
-
公开(公告)号：US4016282A
公开(公告)日：1977-04-05
申请号：US568384
申请日：1975-04-16
IPC分类号： A61K31/43 , C07C275/60
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D499/68
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
摘要翻译： 6-（α-3-酰基 - 脲基乙酰胺基） - 青霉烷酸及其药学上可接受的无毒盐，其中存在于3-位的氮原子的氢原子被取代，对革兰氏阳性和革兰氏阴性有效 感染，特别是克雷伯杆菌感染。
-
4.发明授权Ureidoacetamido-penicillins for treating bacterial infections 失效用于治疗细菌感染的UREIDOACETAMIDO-PENICILLIN
公开(公告)号：US3978223A
公开(公告)日：1976-08-31
申请号：US568419
申请日：1975-04-16
IPC分类号： A61K31/43 , C07C275/60
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D499/68
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
-
公开(公告)号：US3959258A
公开(公告)日：1976-05-25
申请号：US425966
申请日：1973-12-19
IPC分类号： A61K31/43 , C07C275/60 , C07D233/38 , C07D261/18 , C07D307/68 , C07D333/24 , C07D333/38 , C07D499/68 , C07F7/08
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D233/38 , C07D261/18 , C07D307/68 , C07D333/24 , C07D333/38 , C07D499/68 , C07F7/08
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
-
公开(公告)号：US3980792A
公开(公告)日：1976-09-14
申请号：US568477
申请日：1975-04-16
IPC分类号： A61K31/43 , C07C275/60
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D499/68
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
-
公开(公告)号：US3939149A
公开(公告)日：1976-02-17
申请号：US426188
申请日：1973-12-19
IPC分类号： A61K31/43 , C07C275/60 , C07D499/64 , C07D499/46
CPC分类号： C07D499/64 , A61K31/43 , C07C275/60 , C07D499/68
摘要： 6-(.alpha.-3-Acyl-ureidoacetamido)-penicillanic acids and pharmaceutically acceptable non-toxic salts thereof in which the hydrogen atom of the nitrogen atom present in the 3-position is substituted, are effective against Gram-positive and Gram-negative infections, particularly Klebsiella aerobacter infections.
-
公开(公告)号：US3978056A
公开(公告)日：1976-08-31
申请号：US502770
申请日：1974-09-03
IPC分类号： C07D233/38 , C07D275/02 , C07D333/34 , C07D499/00 , C07D499/64 , C07D499/46
CPC分类号： C07D275/02 , C07D233/38 , C07D333/34 , C07D499/00
摘要： Arylmethyl- and cyclohexenylmethyl- penicillins, substituted on the .alpha.-carbon atom of the side chain by a 2,3-disubstituted imidazolidinylcarbamide or a 2,3-disubstituted imidazolidinylthiocarbamido group, or by the corresponding 2,3-disubstituted 1,3-diazacyclohexylcarbamido or thiocarbamido groups are anti-bacterial agents.
摘要翻译： 通过2,3-二取代的咪唑烷基酰胺或2,3-二取代的咪唑烷基硫代氨基甲酰基取代在侧链的α-碳原子上的芳基甲基 - 和环己烯基甲基 - 青霉素，或通过相应的2,3-二取代的1,3-二氮杂环己基氨基甲酰基 或硫代氨基甲酰基是抗菌剂。
-
公开(公告)号：US4009272A
公开(公告)日：1977-02-22
申请号：US605742
申请日：1975-08-18
IPC分类号： C07D499/00 , A61K31/505
CPC分类号： C07D499/00
摘要： Penicillins of the formula ##STR1## or pharmaceutically acceptable non-toxic salts thereof, wherein C* is a carbon atom constituting a center of chirality;A is a moiety of the formula ##STR2## wherein X is ##STR3## Y is ##STR4## WHEREIN Aryl is an aryl moiety; Z is ##STR5## Q.sub.1 is ##STR6## Q.sub.2 is ##STR7## R is straight-chain or branched alkyl of 1 to 5 carbon atoms; R.sub.1 is alkyl of 1 to 10 carbon atoms, cycloalkyl of 3 to 10 carbon atoms, alkenyl of 2 to 10 carbon atoms, cycloalkenyl of 3 to 10 carbon atoms, vinyl, arylvinyl, mono-, di-, or tri-halo-lower alkyl, H.sub.2 N--, R--NH--, (R).sub.2 N--, aryl--NH--, aryl-lower alkylamino, alkoxy of 1 to 8 carbon atoms, aralkoxy of 1 to 8 carbon atoms in the alkoxy portion, cycloalkoxy of 3 to 7 carbon atoms, aryloxy, R--O--V--, R--S--V--, N=C--V--, R--O--CO--V--, H.sub.2 N--CO--V--, R--NH--CO--V--, R--O--CO--NH--, R--SO.sub.2 --NH--, (R).sub.2 N--CO--V--, wherein R is as above defined, ##STR8## provided that when X is --SO.sub.2 --, R.sub.1 is not alkoxy, aralkoxy, cycloalkoxy or aryloxy, and further provided that R.sub.1 can also be hydrogen when X is --CO--;V is a divalent organic radical of 1 to 3 carbon atoms;n is 0, 1 or 2;R.sub.2 and R.sub.3 are the same or different and are each hydrogen, alkyl of 1 to 8 carbon atoms, alkenyl of 2 to 8 carbon atoms, vinyl, allyl, propenyl, cycloalkyl of 3 to 6 carbon atoms, cycloalkenyl of 3 to 6 carbon atoms, mono-, di- or tri-halo lower alkyl or aryl;R.sub.4, r.sub.5 and R.sub.6 are the same or different and are each hydrogen, nitro, cyano, (R).sub.2 N--, (R).sub.2 N--CO--, R--CO--NH--, R--O--CO--, R--CO--O--, R--, R--O--, wherein R is as above defined, H.sub.2 N--SO.sub.2 --, chlorine, bromine, iodine, fluorine, or trifluoromethyl;G is hydrogen or straight or branched chain alkyl of 1 to 5 carbon atoms; andB is a moiety of the formula ##STR9## wherein R.sub.7, R.sub.8 and R.sub.9 are the same or different and are each hydrogen, halogen, nitro, hydroxy, R--, R--O--, R--S--, R--SO--, R--SO.sub.2 --, (R).sub.2 N--, R--CO--NH--, or R--CO--O--, wherein R is as above defined;the arrow in the divalent linking group Q.sub.2 means that the linkage of two atoms by the free valencies of this group must take place as indicated by the arrow;exhibit activity against both Gram-positive and Gram-negative bacteria.This is a division of Ser. No. 502,956, filed Sept. 3, 1974, now U.S. Pat. No. 3,974,142, which in turn is continuation-in-part of our then copending but now abandoned applications Ser. Nos. 299,246 and 300,776, each of which was filed Oct. 20, 1972.
-
公开(公告)号：US3974142A
公开(公告)日：1976-08-10
申请号：US502956
申请日：1974-09-03
IPC分类号： C07D233/38 , C07D275/02 , C07D333/34 , C07D499/00 , C07D499/64 , C07D499/46
CPC分类号： C07D275/02 , C07D233/38 , C07D333/34 , C07D499/00
摘要： Arylmethyl- and cyclohexenylmethyl- penicillins, substituted on the .alpha.carbon atom of the side chain by a 2,3-disubstituted imidazolidinylcarbamido or a 2,3-disubstituted imidazolidinylthiocarbamido group, or by the corresponding 2,3-disubstituted 1,3-diazacyclohexylcarbamido or thiocarbamido groups are anti-bacterial agents.
摘要翻译： 通过2,3-二取代的咪唑烷基氨基甲酰基或2,3-二取代的咪唑烷基硫代氨基甲酰基取代在侧链的α碳原子上的芳基甲基 - 和环己烯基甲基 - 青霉素，或通过相应的2,3-二取代的1,3-二氮杂环己基氨基甲酰基或 硫代氨基甲酰基是抗菌剂。
-
-
-
-
-
-
-
-
-
搜索结果
33 条记录 (耗时 0.045 秒)