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公开(公告)号:US5175301A
公开(公告)日:1992-12-29
申请号:US406515
申请日:1989-09-13
申请人: Isao Minamida , Koichi Iwanaga , Tetsuo Okauchi
发明人: Isao Minamida , Koichi Iwanaga , Tetsuo Okauchi
IPC分类号: C07D213/61 , A01N33/18 , A01N35/08 , A01N43/40 , A01N43/42 , A01N43/60 , A01N43/78 , A01N47/24 , A01N55/00 , C07C211/22 , C07C211/29 , C07C229/34 , C07C243/10 , C07C311/50 , C07D20060101 , C07D213/24 , C07D213/38 , C07D213/40 , C07D213/42 , C07D213/64 , C07D213/70 , C07D213/74 , C07D213/77 , C07D215/12 , C07D215/38 , C07D239/26 , C07D241/12 , C07D277/20 , C07D277/22 , C07D277/28 , C07D277/32 , C07D277/38 , C07D277/42 , C07D295/13 , C07D295/30 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07F7/08
CPC分类号: C07D213/40 , A01N35/08 , A01N43/40 , A01N43/42 , A01N43/60 , A01N43/78 , A01N47/24 , A01N55/00 , C07C211/29 , C07D213/38 , C07D213/42 , C07D213/61 , C07D213/64 , C07D213/70 , C07D213/74 , C07D215/12 , C07D241/12 , C07D277/28 , C07D277/32 , C07D277/42 , C07D401/06 , C07F7/0812
摘要: .alpha.-Unsaturated amines of the formula: ##STR1## wherein X.sup.1 and X.sup.2 are such that one is an electron-attracting group with the other being a hydrogen atom or an electron-attracting group; R.sup.1 is a group attached through a nitrogen atom; R.sup.2 is a hydrogen atom or a group attached through a carbon, nitrogen or oxygen atom; n is an integer equal to 0, 1 or 2; A is a heterocyclic group or a cyclic hydrocarbon group, and salts thereof and their agrochemical use as insecticidal and/or miticidal agents are described.
摘要翻译: 具有下式的α-不饱和胺:其中X1和X2使得一个是吸电子基团,另一个是吸电子基团或吸电子基团; R1是通过氮原子连接的基团; R2是氢原子或通过碳,氮或氧原子连接的基团; n是等于0,1或2的整数; A是杂环基或环状烃基,其盐及其作为杀虫剂和/或杀螨剂的农药用途被描述。
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公开(公告)号:US4963542A
公开(公告)日:1990-10-16
申请号:US353216
申请日:1989-05-17
申请人: Mitsuo Numata , Isao Minamida , Susumu Tsushima
发明人: Mitsuo Numata , Isao Minamida , Susumu Tsushima
IPC分类号: A61K31/545 , C07D501/24 , C07D501/34 , C07D501/36 , C07D501/38 , C07D501/46
CPC分类号: C07D501/34 , C07D501/24
摘要: Disclosed 2-(syn)-hydroxyimino-acetamide derivatives of the formula: ##STR1## wherein Y is hydrogen, hydroxyl, an acyloxy, carbamoyloxy, a quaternary ammonium or a nitrogen-containing heterocyclic ring-substituted thio group; or pharmaceutically acceptable salts or esters thereof are useful as antibacterial agents. Also disclosed are processes for producing them.
摘要翻译: 公开的下式的2-(顺式) - 羟基亚氨基 - 乙酰胺衍生物:其中Y是氢,羟基,酰氧基,氨基甲酰氧基,季铵或含氮杂环取代的硫基; 或其药学上可接受的盐或酯可用作抗菌剂。 还公开了用于生产它们的方法。
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公开(公告)号:US4517361A
公开(公告)日:1985-05-14
申请号:US480791
申请日:1983-03-31
IPC分类号: C07D277/34 , C07D277/36 , C07D501/24 , C07D501/34 , C07D501/36 , C07D501/28
CPC分类号: C07D501/24 , C07D277/34 , C07D277/36
摘要: A compound of the formula: ##STR1## wherein R.sup.1 represents hydrogen or an alkyl group, X represents oxygen or sulfur or a group of formula -NR.sup.2 (where R.sup.2 is hydrogen or an alkyl group and in the case of alkyl, it may form a ring jointed with R.sup.1), and Y represents acetoxy group or a group of formula -SR.sup.3 (where R.sup.3 is a nitrogen-containing heterocyclic group), or a pharmaceutically acceptable salt thereof, is found to have a broad antimicrobial spectrum and, in particular, effective against gram-negative bacteria including Escherichia coli, Klebsiella pneumoniae, Proteus vulgaris, Proteus morganii, as well as gram positive ones. Thus, these compounds may be used for antimicrobial agents in therapeutical purposes.
摘要翻译: 下式的化合物:其中R 1表示氢或烷基,X表示氧或硫或式-NR 2基团(其中R 2是氢或烷基,在烷基的情况下可以形成 环与R 1连接),Y表示乙酰氧基或式-SR 3(其中R 3为含氮杂环基)基团或其药学上可接受的盐具有宽的抗菌谱,特别是, 对革兰氏阴性菌有效,包括大肠杆菌,肺炎克雷伯杆菌,普通变形杆菌,变形杆菌,以及革兰氏阳性菌。 因此,这些化合物可用于治疗目的的抗微生物剂。
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公开(公告)号:US4179502A
公开(公告)日:1979-12-18
申请号:US877746
申请日:1978-02-14
申请人: Mitsuo Numata , Isao Minamida , Susumu Tsushima
发明人: Mitsuo Numata , Isao Minamida , Susumu Tsushima
IPC分类号: A61K31/545 , A61K31/546 , A61P31/04 , C07D501/20 , C07D501/24
CPC分类号: C07D501/20
摘要: 2-Hydroxyiminoacetamide compounds of the following formula and salts thereof: ##STR1## [wherein X is S, O or an imino group which may optionally be substituted; B is a hydrogen atom or a hydroxyl, amino, mercapto or hydrocarbon residue group which may optionally be substituted; and COOR is a carboxyl group which may optionally be esterified] and pharmaceutically acceptable salts thereof are novel and useful as antibacterial agents.
摘要翻译: 下式的2-羟基亚氨基乙酰胺化合物及其盐:其中X是S,O或可任意被取代的亚氨基; B是氢原子或可任选被取代的羟基,氨基,巯基或烃残基; COOR是可任选被酯化的羧基]及其药学上可接受的盐是新颖的,可用作抗菌剂。
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公开(公告)号:US06407248B1
公开(公告)日:2002-06-18
申请号:US07946542
申请日:1992-09-17
申请人: Isao Minamida , Koichi Iwanaga , Tetsuo Okauchi
发明人: Isao Minamida , Koichi Iwanaga , Tetsuo Okauchi
IPC分类号: C07D21326
CPC分类号: C07D213/40 , A01N35/08 , A01N43/40 , A01N43/42 , A01N43/60 , A01N43/78 , A01N47/24 , A01N55/00 , C07C211/29 , C07D213/38 , C07D213/42 , C07D213/61 , C07D213/64 , C07D213/70 , C07D213/74 , C07D215/12 , C07D239/26 , C07D241/12 , C07D277/28 , C07D277/32 , C07D277/42 , C07D401/06 , C07F7/0812
摘要: &agr;-Unsaturated amines of the formula: wherein X1 and X2 are such that one is an electron-attracting group with the other being a hydrogen atom or an electron-attracting group; R1 is a group attached through a nitrogen atom; R2 is a hydrogen atom or a group attached through a carbon, nitrogen or oxygen atom; n is an integer equal to 0, 1 or 2; A is a heterocyclic group or a cyclic hydrocarbon group, and salts thereof and their agrochemical use as insecticidal and/or miticidal agents are described.
摘要翻译: 具有下式的α-不饱和胺:其中X1和X2使得一个是吸电子基团,另一个是吸电子基团或吸电子基团; R1是通过氮原子连接的基团; R2是氢原子或通过碳,氮或氧原子连接的基团; n是等于0,1或2的整数; A是杂环基或环状烃基,其盐及其作为杀虫剂和/或杀螨剂的农药用途被描述。
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公开(公告)号:US5256679A
公开(公告)日:1993-10-26
申请号:US745245
申请日:1991-08-14
IPC分类号: A01N51/00 , A01N43/40 , A01N43/78 , A01N43/84 , A01N47/44 , C07C255/58 , C07C277/08 , C07C279/34 , C07C335/40 , C07D205/10 , C07D207/40 , C07D207/404 , C07D207/44 , C07D207/448 , C07D209/48 , C07D211/88 , C07D213/16 , C07D213/36 , C07D213/61 , C07D213/69 , C07D213/75 , C07D241/12 , C07D277/12 , C07D277/20 , C07D277/28 , C07D277/32 , C07D277/34 , C07D277/38 , C07D277/48 , C07D417/12 , C07D213/26 , C07D277/30
CPC分类号: C07D207/404 , A01N51/00 , C07C255/58 , C07C335/40 , C07D205/10 , C07D207/448 , C07D209/48 , C07D211/88 , C07D213/61 , C07D213/69 , C07D241/12 , C07D277/32 , C07D277/34 , C07D417/12
摘要: Novel substituted nitroguanidine derivatives and salts thereof having the following formula: ##STR1## wherein R.sup.1 is a substituted or unsubstituted heterocyclic group; R.sup.2 is a group attached through a sulfur atom, a group attached through a phosphorus atom, cyano, --CO--OR.sup.6 wherein R.sup.6 is a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or --CO--NR.sup.7 R.sup.8 wherein R.sup.7 and R.sup.8, which are the same or different, are each independently hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or R.sup.7 and R.sup.8, taken together with the nitrogen atom to which they are attached are a cyclic amino group; R.sup.3 is hydrogen, a substituted or unsubstituted hydrocarbon group (except for one substituted with an oxo group at the binding site), a group attached through a sulfur atom, a group attached through a phosphorus atom, cyano, --CO--R.sup.9 wherein R.sup.9 is hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, --CO--OR.sup.10 wherein R.sup.10 is a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or --CO--NR.sup.11 R.sup.12 wherein R.sup.11 and R.sup.12, which are the same or different, are each independently hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or R.sup.11 and R.sup.12, taken together with the nitrogen atom to which they are attached are a cyclic amino group; and R.sup.4 is hydrogen or a lower alkyl group; which have unexpectedly potent pesticidal activity and very low toxicity.
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公开(公告)号:US5214152A
公开(公告)日:1993-05-25
申请号:US655072
申请日:1991-02-14
申请人: Isao Minamida , Koichi Iwanaga , Tetsuo Okauchi
发明人: Isao Minamida , Koichi Iwanaga , Tetsuo Okauchi
IPC分类号: C07D213/61 , A01N33/18 , A01N35/08 , A01N43/40 , A01N43/42 , A01N43/60 , A01N43/78 , A01N47/24 , A01N55/00 , C07C211/22 , C07C211/29 , C07C229/34 , C07C243/10 , C07C311/50 , C07D20060101 , C07D213/24 , C07D213/38 , C07D213/40 , C07D213/42 , C07D213/64 , C07D213/70 , C07D213/74 , C07D213/77 , C07D215/12 , C07D215/38 , C07D239/26 , C07D241/12 , C07D277/20 , C07D277/22 , C07D277/28 , C07D277/32 , C07D277/38 , C07D277/42 , C07D295/13 , C07D295/30 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07F7/08
CPC分类号: C07D213/40 , A01N35/08 , A01N43/40 , A01N43/42 , A01N43/60 , A01N43/78 , A01N47/24 , A01N55/00 , C07C211/29 , C07D213/38 , C07D213/42 , C07D213/61 , C07D213/64 , C07D213/70 , C07D213/74 , C07D215/12 , C07D239/26 , C07D241/12 , C07D277/28 , C07D277/32 , C07D277/42 , C07D401/06 , C07F7/0812
摘要: .alpha.-Unsaturated amines of the formula: ##STR1## wherein X.sup.1 and X.sup.2 are such that one is an electron-attracting group with the other being a hydrogen atom or an electron-attracting group; R.sup.1 is a group attached through a nitrogen atom; R.sup.2 is a hydrogen atom or a group attached through a carbon, nitrogen or oxygen atom; n is an integer equal to 0, 1 or 2; A is a heterocyclic group or a cyclic hydrocarbon group, and salts thereof and their agrochemical use as insecticidal and/or miticidal agents are described.
摘要翻译: α-不饱和胺,其具有下式:其中X1和X2使得一个是吸电子基团,另一个是吸电子基团或吸电子基团; R1是通过氮原子连接的基团; R2是氢原子或通过碳,氮或氧原子连接的基团; n是等于0,1或2的整数; A是杂环基或环状烃基,其盐及其作为杀虫剂和/或杀螨剂的农药用途被描述。
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公开(公告)号:US5180833A
公开(公告)日:1993-01-19
申请号:US666128
申请日:1991-03-07
申请人: Hideki Uneme , Noriko Higuchi , Isao Minamida
发明人: Hideki Uneme , Noriko Higuchi , Isao Minamida
IPC分类号: A01N47/46 , A01N51/00 , C07D277/20 , C07D277/32
CPC分类号: C07D277/32 , A01N51/00
摘要: Novel processes for preparing 2-chlorothiazoles, useful as an intermediate for insecticides, from allyl isothiocyanate derivatives having the formula [II]: ##STR1## wherein X represents a leaving group, are simple and convenient reaction procedures under mild conditions without need of a large excess of a chlorinating agent. Further, processes for preparing 5-(aminomethyl)-2-chlorothiazole or salts thereof from the compound [II] achieve higher yields by simple, convenient and inexpensive procedures.
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公开(公告)号:US4239758A
公开(公告)日:1980-12-16
申请号:US44215
申请日:1979-05-31
IPC分类号: A61K20060101 , A61K31/545 , A61K31/546 , A61P31/04 , C07D20060101 , C07D501/00 , C07D501/04 , C07D501/20 , C07D501/22 , C07D501/24 , C07D501/26 , C07D501/28 , C07D501/34 , C07D501/36 , C07D501/38 , C07D501/46 , C07D501/56 , C07D501/60
CPC分类号: C07D501/20 , C07D501/24
摘要: A novel cephalosporin derivative of the formula: ##STR1## [wherein X is hydrogen, hydroxyl, acyloxy, alkoxy, carbamoyloxy, quaternary ammonium or a group of the formula --SR.sup.1 (where R.sup.1 is a nitrogen-containing heterocyclic group)] or a pharmaceutically acceptable salt or ester thereof is found to have potent antibiotic activity against various bacteria, particularly against gram-negative bacteria such as Escherichia coli, Klebsiella pneumoniae, Proteus vulgaris, Proteus mirabilis, Proteus morganii, Proteus rettgeri and Citrobacter freundii.
摘要翻译: 一种下式的新型头孢菌素衍生物:其中X是氢,羟基,酰氧基,烷氧基,氨基甲酰氧基,季铵或式-SR1(其中R1是含氮杂环基)的基团)或药学上 发现其可接受的盐或酯对各种细菌,特别是对革兰氏阴性细菌如大肠杆菌,肺炎克雷伯杆菌,普通变形杆菌,奇异变形杆菌,变形杆菌,变形杆菌和弗氏氟柠檬酸杆菌具有有效的抗生素活性。
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公开(公告)号:US4172891A
公开(公告)日:1979-10-30
申请号:US783230
申请日:1977-03-31
IPC分类号: A61K20060101 , A61K31/545 , A61K31/546 , A61P31/04 , C07D20060101 , C07D501/00 , C07D501/04 , C07D501/20 , C07D501/22 , C07D501/24 , C07D501/26 , C07D501/28 , C07D501/34 , C07D501/36 , C07D501/38 , C07D501/46 , C07D501/56 , C07D501/60
CPC分类号: C07D501/20 , C07D501/24
摘要: A novel cephalosporin derivative of the formula: ##STR1## [wherein X is hydrogen, hydroxyl, acyloxy, alkoxy, carbamoyloxy, quaternary ammonium or a group of the formula --SR.sup.1 (where R.sup.1 is a nitrogen-containing heterocyclic group)] or a pharmaceutically acceptable salt or ester thereof is found to have potent antibiotic activity against various bacteria, particularly against gram-negative bacteria such as Escherichia coli, Klebsiella pneumoniae, Proteus vulgaris, Proteus mirabilis, Proteus morganii, Proteus rettgeri and Citrobacter freundii.
摘要翻译: 一种下式的新型头孢菌素衍生物:其中X是氢,羟基,酰氧基,烷氧基,氨基甲酰氧基,季铵或式-SR1(其中R1是含氮杂环基)的基团)或药学上 发现其可接受的盐或酯对各种细菌,特别是对革兰氏阴性细菌如大肠杆菌,肺炎克雷伯杆菌,普通变形杆菌,奇异变形杆菌,变形杆菌,变形杆菌和弗氏氟柠檬酸杆菌具有有效的抗生素活性。
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