JP2010516765A5 - - Google Patents
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- Publication number
- JP2010516765A5 JP2010516765A5 JP2009547271A JP2009547271A JP2010516765A5 JP 2010516765 A5 JP2010516765 A5 JP 2010516765A5 JP 2009547271 A JP2009547271 A JP 2009547271A JP 2009547271 A JP2009547271 A JP 2009547271A JP 2010516765 A5 JP2010516765 A5 JP 2010516765A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- methyl
- haloalkyl
- independently
- cycloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- -1 C 1 -C 4 alkoxy Chemical group 0.000 claims 37
- 229910052736 halogen Inorganic materials 0.000 claims 26
- 150000002367 halogens Chemical class 0.000 claims 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims 22
- 229910052799 carbon Inorganic materials 0.000 claims 18
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 14
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 12
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 12
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 125000003545 alkoxy group Chemical group 0.000 claims 11
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 10
- 125000001424 substituent group Chemical group 0.000 claims 10
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 9
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 8
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 8
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 claims 8
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 8
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims 8
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 7
- 125000004432 carbon atom Chemical group C* 0.000 claims 7
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims 6
- 125000005842 heteroatom Chemical group 0.000 claims 6
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 6
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 5
- 150000001721 carbon Chemical group 0.000 claims 5
- 229920006395 saturated elastomer Polymers 0.000 claims 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 125000001188 haloalkyl group Chemical group 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 3
- 125000006660 (C3-C4) halocycloalkyl group Chemical group 0.000 claims 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 3
- 230000000844 anti-bacterial effect Effects 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000002619 bicyclic group Chemical group 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000006699 (C1-C3) hydroxyalkyl group Chemical group 0.000 claims 1
- FCNIGHUELHMMFP-HSZRJFAPSA-N 1-[4-[4-[[methyl-[(1r)-1,2,3,4-tetrahydronaphthalen-1-yl]amino]methyl]-1,3-thiazol-2-yl]piperidin-1-yl]-2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]ethanone Chemical compound CN([C@H]1C2=CC=CC=C2CCC1)CC(N=1)=CSC=1C(CC1)CCN1C(=O)CN1N=C(C(F)(F)F)C=C1C FCNIGHUELHMMFP-HSZRJFAPSA-N 0.000 claims 1
- PWHXKPYWBIBCDO-JOCHJYFZSA-N 2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-1-[4-[4-[[[(1r)-1,2,3,4-tetrahydronaphthalen-1-yl]amino]methyl]-1,3-thiazol-2-yl]piperidin-1-yl]ethanone Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(CN[C@H]3C4=CC=CC=C4CCC3)N=2)CC1 PWHXKPYWBIBCDO-JOCHJYFZSA-N 0.000 claims 1
- ZXLYYQUMYFHCLQ-UHFFFAOYSA-N 2-methylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C)C(=O)C2=C1 ZXLYYQUMYFHCLQ-UHFFFAOYSA-N 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims 1
- 239000003899 bactericide agent Substances 0.000 claims 1
- 230000006315 carbonylation Effects 0.000 claims 1
- 238000005810 carbonylation reaction Methods 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- VORVRNZIGUYKLK-UHFFFAOYSA-N ethyl 3-[4-[4-[methyl(1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl]-1,3-thiazol-2-yl]piperidin-1-yl]-2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-3-oxopropanoate Chemical compound C1CC(C=2SC=C(N=2)C(=O)N(C)C2C3=CC=CC=C3CCC2)CCN1C(=O)C(C(=O)OCC)N1N=C(C(F)(F)F)C=C1C VORVRNZIGUYKLK-UHFFFAOYSA-N 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- RLXUEAXMBWCECP-HSZRJFAPSA-N n-methyl-2-[1-[3-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]propanoyl]piperidin-4-yl]-n-[(1r)-1,2,3,4-tetrahydronaphthalen-1-yl]-1,3-thiazole-4-carboxamide Chemical compound CN([C@H]1C2=CC=CC=C2CCC1)C(=O)C(N=1)=CSC=1C(CC1)CCN1C(=O)CCN1N=C(C(F)(F)F)C=C1C RLXUEAXMBWCECP-HSZRJFAPSA-N 0.000 claims 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89779207P | 2007-01-25 | 2007-01-25 | |
| US60/897,792 | 2007-01-25 | ||
| PCT/US2008/000786 WO2008091580A2 (en) | 2007-01-25 | 2008-01-18 | Fungicidal amides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010516765A JP2010516765A (ja) | 2010-05-20 |
| JP2010516765A5 true JP2010516765A5 (enExample) | 2011-03-10 |
| JP5337711B2 JP5337711B2 (ja) | 2013-11-06 |
Family
ID=39544991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009547271A Expired - Fee Related JP5337711B2 (ja) | 2007-01-25 | 2008-01-18 | 殺菌性アミド |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8420673B2 (enExample) |
| EP (1) | EP2121660B1 (enExample) |
| JP (1) | JP5337711B2 (enExample) |
| CN (1) | CN101622245B (enExample) |
| BR (1) | BRPI0806214A2 (enExample) |
| ES (1) | ES2531256T3 (enExample) |
| PL (1) | PL2121660T3 (enExample) |
| WO (1) | WO2008091580A2 (enExample) |
Families Citing this family (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR036872A1 (es) * | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| TW200738701A (en) * | 2005-07-26 | 2007-10-16 | Du Pont | Fungicidal carboxamides |
| US9090604B2 (en) | 2006-07-27 | 2015-07-28 | E I Du Pont De Nemours And Company | Fungicidal azocyclic amides |
| WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
| TWI428091B (zh) | 2007-10-23 | 2014-03-01 | Du Pont | 殺真菌劑混合物 |
| AU2014202324B2 (en) * | 2007-10-23 | 2016-05-19 | Corteva Agriscience Llc | Fungicidal compounds and mixtures |
| CN103965187A (zh) | 2008-01-25 | 2014-08-06 | 杜邦公司 | 杀真菌杂环化合物 |
| WO2010037479A1 (de) * | 2008-10-01 | 2010-04-08 | Bayer Cropscience Ag | Heterocyclyl substituierte thiazole als pflanzenschutzmittel |
| ES2452299T3 (es) * | 2008-12-02 | 2014-03-31 | E. I. Du Pont De Nemours And Company | Compuestos heterocíclicos fungicidas |
| WO2010066353A1 (de) | 2008-12-11 | 2010-06-17 | Bayer Cropscience Ag | Thiazolyoximether und -hydrazone asl pflanzenschutzmittel |
| DE102010000662A1 (de) | 2009-03-18 | 2010-10-21 | Bayer Cropscience Ag | Aminopropylthiazol-Derivate als Fungizide |
| CA2757415C (en) | 2009-04-02 | 2018-02-06 | Merck Patent Gmbh | Autotaxin inhibitors |
| EP2272846A1 (de) * | 2009-06-23 | 2011-01-12 | Bayer CropScience AG | Thiazolylpiperidin Derivate als Fungizide |
| KR20120089644A (ko) | 2009-08-12 | 2012-08-13 | 신젠타 파티서페이션즈 아게 | 살미생물성 헤테로사이클 |
| UA107938C2 (en) | 2009-08-12 | 2015-03-10 | Syngenta Participations Ag | Heterocycles with microbicidal properties |
| CN102712634B (zh) * | 2009-10-30 | 2016-04-06 | 拜耳知识产权有限责任公司 | 杂芳基哌啶和杂芳基哌嗪衍生物 |
| WO2011056291A1 (en) * | 2009-11-06 | 2011-05-12 | Bayer Cropscience Ag | Use of succinate dehydrogenase inhibitors for extending shelf life of fruits and vegetables |
| EP2516426B1 (de) | 2009-12-21 | 2015-09-16 | Bayer CropScience AG | Bis(difluormethyl)pyrazole als fungizide |
| US8629286B2 (en) * | 2009-12-22 | 2014-01-14 | Syngenta Crop Protection, Llc | Pyrazole derivatives |
| JP5960683B2 (ja) | 2010-04-28 | 2016-08-02 | 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 | 殺真菌剤としてのケトヘテロアリールピペリジンおよび−ピペラジン誘導体 |
| US8815775B2 (en) | 2010-05-18 | 2014-08-26 | Bayer Cropscience Ag | Bis(difluoromethyl)pyrazoles as fungicides |
| BR112012030184A2 (pt) | 2010-05-27 | 2015-12-29 | Bayer Cropscience Ag | derivados de ácido piridinilcarboxílico como fungicidas |
| US20120122928A1 (en) | 2010-08-11 | 2012-05-17 | Bayer Cropscience Ag | Heteroarylpiperidine and -Piperazine Derivatives as Fungicides |
| US8759527B2 (en) | 2010-08-25 | 2014-06-24 | Bayer Cropscience Ag | Heteroarylpiperidine and -piperazine derivatives as fungicides |
| EP2423210A1 (de) | 2010-08-25 | 2012-02-29 | Bayer CropScience AG | Heteroarylpiperidin- und -piperazinderivate als Fungizide |
| CN101971832A (zh) * | 2010-10-20 | 2011-02-16 | 华南理工大学 | 氯虫苯甲酰胺与鱼藤酮复配杀虫微乳剂及其制备方法 |
| CN101971831A (zh) * | 2010-10-20 | 2011-02-16 | 华南理工大学 | 氟虫双酰胺与鱼藤酮复配杀虫微乳剂及其制备方法 |
| CN101971830B (zh) * | 2010-10-20 | 2013-09-25 | 华南理工大学 | 氯虫苯甲酰胺与鱼藤酮复配杀虫水分散粒剂及其制备方法 |
| CN101971833B (zh) * | 2010-10-20 | 2014-04-02 | 华南理工大学 | 氟虫双酰胺与鱼藤酮复配杀虫水分散粒剂及其制备方法 |
| MX352731B (es) | 2010-10-27 | 2017-12-06 | Bayer Ip Gmbh | Derivados de heteroarilpiperidina y -piperazina como fungicidas. |
| BR112013012621A2 (pt) | 2010-11-25 | 2016-07-12 | Syngenta Participations Ag | heterociclos microbicidas |
| KR101848116B1 (ko) | 2011-02-01 | 2018-04-11 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 살진균제로서의 헤테로아릴 피페리딘 및 헤테로아릴 피페라진 유도체 |
| EP2673272A1 (en) * | 2011-02-10 | 2013-12-18 | Syngenta Participations AG | Microbiocidal pyrazole derivatives |
| US8748432B2 (en) | 2011-02-10 | 2014-06-10 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| IN2014CN01862A (enExample) | 2011-09-15 | 2015-05-29 | Bayer Ip Gmbh | |
| BR112014009086A2 (pt) | 2011-10-18 | 2017-05-09 | Syngenta Participations Ag | derivados pirazol microbicidas |
| US20140228372A1 (en) * | 2011-10-18 | 2014-08-14 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| US9480669B2 (en) | 2015-01-06 | 2016-11-01 | The Regents Of The University Of California | Method of destroying and preventing bacterial and fungal biofilm by amino acid infusion |
| US9549904B2 (en) | 2012-06-06 | 2017-01-24 | Thomas Bryan | Method of destroying bacterial biofilm using sterile intravenous or intracavernous glycerin |
| EP2921492B1 (de) | 2011-12-27 | 2017-09-06 | Bayer Intellectual Property GmbH | Heteroarylpiperidin- und -heteroarylpiperazinderivate |
| CN102550573B (zh) * | 2012-01-30 | 2013-10-30 | 华南理工大学 | 氯虫苯甲酰胺与鱼藤酮复配悬浮剂及其制备方法 |
| PL2809668T3 (pl) | 2012-02-02 | 2018-02-28 | Idorsia Pharmaceuticals Ltd | Związki 4-(benzimidazol-2-ilo)tiazolowowe i pokrewne aza-pochodne |
| US20150065481A1 (en) | 2012-03-02 | 2015-03-05 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2013127784A1 (en) | 2012-03-02 | 2013-09-06 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2013127808A1 (en) | 2012-03-02 | 2013-09-06 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| EP2864326A1 (en) | 2012-06-22 | 2015-04-29 | E. I. Du Pont de Nemours and Company | Fungicidal heterocyclic compounds |
| DK2890682T3 (en) | 2012-08-30 | 2016-09-12 | Bayer Cropscience Ag | METHOD OF DECARBOXYLATION OF 3,5-BIS (HALOGENALKYL) -PYRAZOL-4-CARBOXYLIC ACID DERIVATIVES |
| WO2014060176A1 (en) | 2012-10-16 | 2014-04-24 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2014075874A1 (en) * | 2012-11-13 | 2014-05-22 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2014075873A1 (en) * | 2012-11-13 | 2014-05-22 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2014118142A1 (en) | 2013-02-01 | 2014-08-07 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2014118143A1 (en) | 2013-02-04 | 2014-08-07 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| WO2014154530A1 (en) | 2013-03-25 | 2014-10-02 | Syngenta Participations Ag | Microbiocidal pyrazole derivatives |
| EP2801575A1 (en) | 2013-05-07 | 2014-11-12 | Bayer CropScience AG | Heteroaryldihydropyridine derivatives as fungicides |
| DK3013821T3 (en) | 2013-06-24 | 2018-06-18 | Bayer Cropscience Ag | PIPERIDINCARBOXYLIC ACID DERIVATIVES AS FUNGICIDES |
| PL3024832T3 (pl) | 2013-07-22 | 2018-10-31 | Idorsia Pharmaceuticals Ltd | Pochodne 1-(piperazyn-1-ylo)-2-([1,2,4]triazol-1-ilo)-etanonu |
| JP6408582B2 (ja) | 2013-08-28 | 2018-10-17 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺菌剤としてのヘテロアリールピペリジン及びヘテロアリールピペラジンのマロン酸エステル誘導体 |
| JP2017512788A (ja) | 2014-03-24 | 2017-05-25 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺菌剤としてのフェニルピペリジンカルボキサミド誘導体 |
| AR099789A1 (es) | 2014-03-24 | 2016-08-17 | Actelion Pharmaceuticals Ltd | Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina |
| WO2016024350A1 (ja) | 2014-08-13 | 2016-02-18 | 株式会社エス・ディー・エス バイオテック | 縮合１１員環化合物及びそれらを含有する農園芸用殺菌剤 |
| CA2972401C (en) | 2014-12-30 | 2023-09-05 | Dow Agrosciences Llc | Picolinamide compounds with fungicidal activity |
| MX2017009288A (es) | 2015-01-15 | 2017-10-11 | Idorsia Pharmaceuticals Ltd | Derivados de hidroxialquil-piperazina como moduladores del receptor cxcr3. |
| AR103399A1 (es) | 2015-01-15 | 2017-05-10 | Actelion Pharmaceuticals Ltd | Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3 |
| JP6407457B2 (ja) | 2016-02-08 | 2018-10-17 | 株式会社エス・ディー・エス バイオテック | １，２−ベンゼンジメタノール化合物の製造方法 |
| EP3415008A4 (en) | 2016-02-08 | 2019-09-11 | SDS Biotech K. K. | GERMIC COMPOSITION |
| TW201902357A (zh) * | 2017-05-02 | 2019-01-16 | 美商陶氏農業科學公司 | 用作種子處理之無環吡啶醯胺 |
| WO2018226987A1 (en) | 2017-06-07 | 2018-12-13 | The Regents Of The University Of California | Compositions for treating fungal and bacterial biofilms and methods of using the same |
| WO2020117755A1 (en) | 2018-12-03 | 2020-06-11 | The Regents Of The University Of California | Compositions and methods for treating biofilms |
| WO2022042613A1 (zh) * | 2020-08-27 | 2022-03-03 | 上海和誉生物医药科技有限公司 | 一种1h-吡唑-4-酰胺衍生物，其制备方法和应用 |
| CN113994804A (zh) * | 2021-11-01 | 2022-02-01 | 恩平市农业技术推广服务中心 | 基于目标产量的冬作马铃薯平衡施肥专家系统 |
| US12109176B1 (en) | 2023-04-20 | 2024-10-08 | Thomas Bryan | Effect of glycerol on biofilm forming bacteria and fungi that changes the microbes sensitivity to pro and anti-biofilm non-toxic, non-bonded plasma amino acids and amino acid derivatives |
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-
2008
- 2008-01-18 ES ES08724674T patent/ES2531256T3/es active Active
- 2008-01-18 EP EP08724674.0A patent/EP2121660B1/en not_active Not-in-force
- 2008-01-18 JP JP2009547271A patent/JP5337711B2/ja not_active Expired - Fee Related
- 2008-01-18 WO PCT/US2008/000786 patent/WO2008091580A2/en not_active Ceased
- 2008-01-18 BR BRPI0806214-5A patent/BRPI0806214A2/pt not_active Application Discontinuation
- 2008-01-18 US US12/521,156 patent/US8420673B2/en not_active Expired - Fee Related
- 2008-01-18 PL PL08724674T patent/PL2121660T3/pl unknown
- 2008-01-18 CN CN200880003021.1A patent/CN101622245B/zh not_active Expired - Fee Related