AR042716A1 - Derivados de benzoilo substituidos como herbicidas - Google Patents
Derivados de benzoilo substituidos como herbicidasInfo
- Publication number
- AR042716A1 AR042716A1 ARP040100030A ARP040100030A AR042716A1 AR 042716 A1 AR042716 A1 AR 042716A1 AR P040100030 A ARP040100030 A AR P040100030A AR P040100030 A ARP040100030 A AR P040100030A AR 042716 A1 AR042716 A1 AR 042716A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halogen
- alkoxy
- radicals
- hydrogen
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 11
- -1 (C1 -6) -SO2OR4 Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 150000002431 hydrogen Chemical class 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000006413 ring segment Chemical group 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- MZAGXDHQGXUDDX-JSRXJHBZSA-N (e,2z)-4-ethyl-2-hydroxyimino-5-nitrohex-3-enamide Chemical compound [O-][N+](=O)C(C)C(/CC)=C/C(=N/O)/C(N)=O MZAGXDHQGXUDDX-JSRXJHBZSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/10—Oxygen atoms
- C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/18—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member containing only hydrogen and carbon atoms in addition to the ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Furan Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Reivindicación 1: Compuestos de la fórmula general (1) o sus sales, en la cual los radicales e índices tienen los significados: R1, R2 significan, independientemente uno de otro, hidrógeno, mercapto, nitro, halógeno, ciano, rodano, alquilo C1-6, halógenoalquilo C1-6, alquenilo C2-6, halógenoalquilo C2-6, alquinilo C2-6, halógenoalquinilo C3-6, cicloalquilo C3-6, OR4, OCOR4, OSO2R4, S(O)nR4, SO2OR4, SO2N(R4)2, NR4SO2R4, NR4COR4, alquilo(C1-6)-S(O)nR4, alquilo(C1-6)-OR4, alquilo(C1-6)-OCOR4, alquilo(C1-6)-OSO2R4, alquilo(C1-6)-SO2OR4, alquilo(C1-6)-SO2N(R4)2 o alquilo(C1-6)-NR4COR4; R3 significa hidrógeno, alquilo C1-6, alquenilo C2-6 o alquinilo C2-6; R4 significa hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C1-6, fenilo o fenil-alquilo (C1-6), estando los seis radicales mencionados en último lugar sustituidos con s radicales del grupo hidroxilo, mercapto, amino, ciano, nitro, rodano, OR3, SR3, N(R3)2, =NOR3, OCOR3, SCOR3, NR3COR3, CO2R3, COSR3, CON(R3)2, alquil(C1-4)-iminoxilo, alcoxi(C1-4)amino, alquil(C1-4)-carbonilo, alcoxi(C1-4)-alcoxi(C2-6)-carbonilo y alquil(C1-4)-sulfonilo; Het significa un grupo heterocíclico completamente saturado, cuyos átomos anulares consisten en carbono o oxígeno, en el cual el número total de los átomos anulares es de p, el número de átomos de oxígeno es de r, el número de átomos de carbono es de (p-r), y Het puede estar sustituido por n radicales R5; n significa 0, 1 ó 2; p significa 5, 6 ó 7; r significa 1 ó 2; s significa 0, 1, 2 ó 3; X significa O o S/(O)n; R5 significa hidroxilo, mercapto, amino, ciano, nitro, halógeno, formilo, alquil(C1-6)amino, dialquil(C1-6)-amino, alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquil(C1-4)-carboniloxilo, alquilo C1-6, halógenoalquilo C1-6, alquiltio C1-6, halógenoalquiltio C1-6, alcoxilo C1-6, halógenoalcoxilo C1-6 o R5 forma conjuntamente con el átomo de carbono al que está unido un grupo carbonilo; Q significa un radical de resto de grupo de fórmula (2); R6, R7 significan, independientemente uno de otro, hidrógeno, alquilo C1-6, halógenoalquilo C1-6, o ciclopropilo C3-6; R8 significa hidrógeno, alquilo C1-6, halógenoalquilo C1-6, alquil(C1-6)-carbonilo, halógenoalquil(C1-6)-carbonilo, alcoxi(C1-6)-carbonilo, alquil(C1-6)-sulfonilo, halógenoalquil(C1-6)-sulfonilo, fenil-carbonilo, fenilcarbonilmetilo, feniloxicarbonilo o fenilsulfonilo, estando los núcleos de fenilo de los cuatro radicales mencionados en último lugar sustituidos con s radicales del grupo de halógeno, nitro, ciano, alquilo C1-6, halógenoalquilo C1-6, alcoxilo C1-6 y halógeno-alcoxilo C1-6;
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10301110A DE10301110A1 (de) | 2003-01-09 | 2003-01-09 | Substituierte Benzoylderivate als Herbizide |
Publications (1)
Publication Number | Publication Date |
---|---|
AR042716A1 true AR042716A1 (es) | 2005-06-29 |
Family
ID=32519950
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP040100030A AR042716A1 (es) | 2003-01-09 | 2004-01-07 | Derivados de benzoilo substituidos como herbicidas |
Country Status (26)
Country | Link |
---|---|
US (2) | US20040167029A1 (es) |
EP (1) | EP1585742B1 (es) |
JP (1) | JP4592424B2 (es) |
KR (1) | KR101126950B1 (es) |
CN (1) | CN100349889C (es) |
AR (1) | AR042716A1 (es) |
AT (1) | ATE369358T1 (es) |
AU (1) | AU2003293859B2 (es) |
BR (1) | BR0317970B1 (es) |
CA (1) | CA2513000C (es) |
CO (1) | CO5700821A2 (es) |
DE (2) | DE10301110A1 (es) |
DK (1) | DK1585742T3 (es) |
EA (1) | EA009609B1 (es) |
ES (1) | ES2290542T3 (es) |
HR (1) | HRP20050628A2 (es) |
IL (1) | IL169542A0 (es) |
MX (1) | MXPA05007409A (es) |
MY (1) | MY136628A (es) |
PL (1) | PL378542A1 (es) |
PT (1) | PT1585742E (es) |
RS (1) | RS20050519A (es) |
TW (1) | TW200505337A (es) |
UA (1) | UA81796C2 (es) |
WO (1) | WO2004063187A1 (es) |
ZA (1) | ZA200504896B (es) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004029307A1 (de) * | 2004-06-17 | 2005-12-29 | Bayer Cropscience Gmbh | Substituierte Benzoylcyclohexandione als Herbizide |
DE102004029308A1 (de) * | 2004-06-17 | 2005-12-29 | Bayer Cropscience Gmbh | Substituierte Benzoylpyrazole als Herbiszide |
DK2611785T3 (da) | 2010-09-01 | 2014-08-25 | Bayer Ip Gmbh | N-(tetrazol-5yl)- og n- (triazol-5-yl) arylcarboxylsyreamider og deres anvendelse som herbicider |
CN102464630B (zh) * | 2010-11-19 | 2015-05-13 | 中国中化股份有限公司 | 含氮杂环取代的苯甲酰基类化合物及其应用 |
LT2688885T (lt) | 2011-03-22 | 2016-09-12 | Bayer Intellectual Property Gmbh | N-(1,3,4-oksadiazol-2-il)arilkarboksamidai ir jų panaudojimas kaip herbicidų |
CA2830802A1 (en) | 2011-03-25 | 2012-10-04 | Bayer Intellectual Property Gmbh | Use of n-(1,2,5-oxadiazol-3-yl)benzamides for controlling unwanted plants in areas of transgenic crop plants being tolerant to hppd inhibitor herbicides |
JP6078065B2 (ja) | 2011-08-03 | 2017-02-08 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | N−(テトラゾール−5−イル)アリールカルボキサミド類及びn−(トリアゾール−5−イル)アリールカルボキサミド類並びに除草剤としてのそれらの使用 |
UA116532C2 (uk) | 2011-12-13 | 2018-04-10 | Байєр Інтеллектуал Проперті Гмбх | Аміди n-(1,2,5-оксадіазол-3-іл)-, n-(1,3,4-оксадіазол-2-іл)- або n-(тетразол-5-іл)арилкарбоксильної кислоти й застосування їх як гербіцидів |
WO2013104705A1 (de) | 2012-01-11 | 2013-07-18 | Bayer Intellectual Property Gmbh | Tetrazol-5-yl- und triazol-5-yl-arylverbindungen und ihre verwendung als herbizide |
CN104125949B (zh) * | 2012-02-21 | 2016-04-13 | 拜耳知识产权有限责任公司 | 除草的3-(亚磺酰亚氨基/磺酰亚氨基)-苯甲酰胺 |
WO2014086734A1 (de) | 2012-12-06 | 2014-06-12 | Bayer Cropscience Ag | N-(oxazol-2-yl)-arylcarbonsäureamide und ihre verwendung als herbizide |
AU2016330250A1 (en) | 2015-09-28 | 2018-03-29 | Bayer Cropscience Aktiengesellschaft | Acylated N-(1,2,5-oxadiazole-3-yl)-, N-(1,3,4-oxadiazole-2-yl)-, n-(tetrazole-5-yl)- and N-(triazole-5-yl)-aryl carboxamides, and use thereof as herbicides |
CN105601548A (zh) * | 2016-01-18 | 2016-05-25 | 黑龙江大学 | 苯甲酰类化合物、含有该化合物的组合物及其应用 |
WO2017144402A1 (de) | 2016-02-24 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | N-(5-halogen-1,3,4-oxadiazol-2-yl)arylcarbonsäureamide und ihre verwendung als herbizide |
CN108264484A (zh) * | 2016-12-30 | 2018-07-10 | 浙江省化工研究院有限公司 | 一种带醚结构的取代的苯基酮类化合物、其制备方法及应用 |
CN110520414B (zh) | 2017-03-30 | 2023-11-28 | 拜耳作物科学股份公司 | 取代的n-(-1,3,4-噁二唑-2-基)芳基羧酰胺及其作为除草剂的用途 |
AU2020209871A1 (en) | 2019-01-14 | 2021-08-05 | Bayer Aktiengesellschaft | Herbicidal substituted n-tetrazolyl aryl carboxamides |
CN111559965B (zh) * | 2019-02-14 | 2022-11-18 | 东莞市东阳光农药研发有限公司 | 取代的苯甲酰类化合物及其在农业中的应用 |
CN111808024B (zh) * | 2019-04-11 | 2023-06-27 | 郑州手性药物研究院有限公司 | 一种苯基吡唑酮类化合物或其盐、制备方法和应用 |
CN112645853A (zh) * | 2019-10-10 | 2021-04-13 | 江西天宇化工有限公司 | 一种2-氯-3-烷氧基甲基-4-甲磺酰基苯甲酸的制备方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE789105A (fr) * | 1971-09-21 | 1973-03-21 | Fmc Corp | Dioxannes substitues et leur application comme |
DE2709144A1 (de) * | 1977-03-03 | 1978-09-07 | Bayer Ag | Tetrahydrofuranaether-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide |
ZA829035B (en) * | 1981-12-16 | 1983-09-28 | Shell Res Ltd | Oxabicycloalkane herbicides |
DE3738536A1 (de) * | 1987-11-13 | 1989-05-24 | Basf Ag | Benzylether, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwachstums |
US6274600B1 (en) * | 1995-06-05 | 2001-08-14 | The Regents Of The University Of California | Heteroatom substituted benzoyl derivatives that enhance synaptic responses mediated by AMPA receptors |
JP4592183B2 (ja) * | 1997-08-07 | 2010-12-01 | ビーエーエスエフ ソシエタス・ヨーロピア | 2−ベンゾイルシクロヘキサン−1,3−ジオン |
DE59814330D1 (de) * | 1997-08-07 | 2009-02-26 | Basf Se | Heterocyclisch substituierte 4-benzoyl-pyrazole als herbizide |
WO2000037437A1 (en) * | 1998-12-21 | 2000-06-29 | Syngenta Participations Ag | Novel herbicides |
DE19961466A1 (de) * | 1998-12-21 | 2000-07-06 | Novartis Ag | Neue Herbizide |
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2003
- 2003-01-09 DE DE10301110A patent/DE10301110A1/de not_active Withdrawn
- 2003-12-12 AU AU2003293859A patent/AU2003293859B2/en not_active Ceased
- 2003-12-12 EP EP03789245A patent/EP1585742B1/de not_active Expired - Lifetime
- 2003-12-12 UA UAA200507872A patent/UA81796C2/uk unknown
- 2003-12-12 CA CA2513000A patent/CA2513000C/en not_active Expired - Fee Related
- 2003-12-12 AT AT03789245T patent/ATE369358T1/de not_active IP Right Cessation
- 2003-12-12 DK DK03789245T patent/DK1585742T3/da active
- 2003-12-12 JP JP2004565967A patent/JP4592424B2/ja not_active Expired - Fee Related
- 2003-12-12 KR KR1020057012754A patent/KR101126950B1/ko not_active IP Right Cessation
- 2003-12-12 EA EA200501049A patent/EA009609B1/ru not_active IP Right Cessation
- 2003-12-12 PT PT03789245T patent/PT1585742E/pt unknown
- 2003-12-12 ES ES03789245T patent/ES2290542T3/es not_active Expired - Lifetime
- 2003-12-12 CN CNB2003801085473A patent/CN100349889C/zh not_active Expired - Fee Related
- 2003-12-12 PL PL378542A patent/PL378542A1/pl not_active Application Discontinuation
- 2003-12-12 MX MXPA05007409A patent/MXPA05007409A/es active IP Right Grant
- 2003-12-12 BR BRPI0317970-2A patent/BR0317970B1/pt not_active IP Right Cessation
- 2003-12-12 WO PCT/EP2003/014129 patent/WO2004063187A1/de active IP Right Grant
- 2003-12-12 RS YUP-2005/0519A patent/RS20050519A/sr unknown
- 2003-12-12 DE DE50307914T patent/DE50307914D1/de not_active Expired - Lifetime
-
2004
- 2004-01-07 AR ARP040100030A patent/AR042716A1/es unknown
- 2004-01-07 TW TW093100363A patent/TW200505337A/zh unknown
- 2004-01-08 US US10/754,081 patent/US20040167029A1/en not_active Abandoned
- 2004-01-08 MY MYPI20040048A patent/MY136628A/en unknown
-
2005
- 2005-06-15 ZA ZA200504896A patent/ZA200504896B/en unknown
- 2005-07-05 IL IL169542A patent/IL169542A0/en unknown
- 2005-07-07 CO CO05066876A patent/CO5700821A2/es not_active Application Discontinuation
- 2005-07-08 HR HR20050628A patent/HRP20050628A2/xx not_active Application Discontinuation
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2007
- 2007-05-30 US US11/807,820 patent/US7569519B2/en not_active Expired - Fee Related
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