MX372721B - Ánalogos halogenados de agentes antifi-broticos. - Google Patents
Ánalogos halogenados de agentes antifi-broticos.Info
- Publication number
- MX372721B MX372721B MX2016000325A MX2016000325A MX372721B MX 372721 B MX372721 B MX 372721B MX 2016000325 A MX2016000325 A MX 2016000325A MX 2016000325 A MX2016000325 A MX 2016000325A MX 372721 B MX372721 B MX 372721B
- Authority
- MX
- Mexico
- Prior art keywords
- antifibrotic agents
- halogenated analogues
- halogenated
- agents
- analogues
- Prior art date
Links
- 230000003510 anti-fibrotic effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/004—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with organometalhalides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/38—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
- C07C237/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
- C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
- C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1613407P | 2007-12-21 | 2007-12-21 | |
| PCT/AU2008/001868 WO2009079692A1 (en) | 2007-12-21 | 2008-12-19 | Halogenated analogues of anti-fibrotic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX372721B true MX372721B (es) | 2020-05-11 |
Family
ID=40800565
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2016000325A MX372721B (es) | 2007-12-21 | 2008-12-19 | Ánalogos halogenados de agentes antifi-broticos. |
| MX2010006787A MX337320B (es) | 2007-12-21 | 2008-12-19 | Análogos halogenados de agentes anti-fibroticos. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2010006787A MX337320B (es) | 2007-12-21 | 2008-12-19 | Análogos halogenados de agentes anti-fibroticos. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8624056B2 (enExample) |
| EP (2) | EP2220028B1 (enExample) |
| JP (2) | JP5730578B2 (enExample) |
| KR (2) | KR20160017139A (enExample) |
| CN (2) | CN102164887A (enExample) |
| AU (1) | AU2008341010B2 (enExample) |
| CA (1) | CA2709937C (enExample) |
| MX (2) | MX372721B (enExample) |
| NZ (1) | NZ584613A (enExample) |
| SG (1) | SG10201506526QA (enExample) |
| WO (1) | WO2009079692A1 (enExample) |
| ZA (1) | ZA201003376B (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8765812B2 (en) | 2006-07-05 | 2014-07-01 | Fibrotech Therapeutics Pty Ltd | Therapeutic compounds |
| JP5730578B2 (ja) | 2007-12-21 | 2015-06-10 | フィブロテック セラピューティクス プロプライエタリー リミテッド | 抗線維症剤のハロゲン化類似体 |
| IN2012DN03312A (enExample) | 2009-10-22 | 2015-10-23 | Fibrotech Therapeutics Pty Ltd | |
| NZ609144A (en) * | 2010-11-24 | 2014-08-29 | Occurx Pty Ltd | Methods of treating eye diseases associated with inflammation and vascular proliferation |
| AU2014233055B2 (en) * | 2013-03-15 | 2018-08-09 | Board Of Regents, The University Of Texas System | Inhibition of pulmonary fibrosis with nutlin-3a and peptides |
| ES2806027T3 (es) * | 2013-11-26 | 2021-02-16 | Univ Yale | Nuevas composiciones penetrantes de células y métodos de uso de las mismas |
| JP6533997B2 (ja) * | 2014-12-26 | 2019-06-26 | 株式会社ヤクルト本社 | Ｚｎｆ１４３阻害活性を有する化合物およびその利用 |
| EP3577103A1 (en) | 2017-02-03 | 2019-12-11 | Certa Therapeutics Pty Ltd. | Anti-fibrotic compounds |
| CN110357789B (zh) * | 2018-04-11 | 2022-09-30 | 华东理工大学 | 作为dhodh抑制剂的n-取代丙烯酰胺衍生物及其制备和用途 |
| AU2022238294A1 (en) * | 2021-03-17 | 2023-10-05 | Occurx Pty Ltd | Compounds for the treatment of disorders and salts and polymorphs thereof |
| CN116730977A (zh) * | 2022-03-04 | 2023-09-12 | 华东理工大学 | 新型芳基杂环类化合物及其制备方法和用途 |
Family Cites Families (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5640710B2 (enExample) * | 1973-01-18 | 1981-09-22 | ||
| JPS5830302B2 (ja) | 1974-04-16 | 1983-06-28 | キツセイヤクヒンコウギヨウ カブシキガイシヤ | シンキホウコウゾクカルボンサンアミドユウドウタイ ノ セイゾウホウホウ |
| JPS5848545B2 (ja) | 1974-04-18 | 1983-10-28 | キツセイヤクヒンコウギヨウ カブシキガイシヤ | シンキホウコウゾクカルボンサンアミドユウドウタイ ノ セイゾウホウホウ |
| JPS511440A (ja) | 1974-04-18 | 1976-01-08 | Kissei Pharmaceutical | Shinkihokozokukarubonsanjudotai no seizohoho |
| GB1484413A (en) * | 1974-04-18 | 1977-09-01 | Kissei Pharmaceutical | Aromatic amidocarboxylic acid derivatives |
| JPS5576852A (en) | 1978-12-01 | 1980-06-10 | Hisamitsu Pharmaceut Co Inc | Novel derivative of anthranilic acid |
| JPS5817186B2 (ja) | 1981-01-23 | 1983-04-05 | キツセイ薬品工業株式会社 | 新規芳香族カルボン酸誘導体の製造方法 |
| US4587356A (en) * | 1981-09-01 | 1986-05-06 | Kissei Pharmaceutical Co., Ltd. | Process for the production of nuclear substituted cinnamoylanthranilic acid derivatives |
| JPS5838244A (ja) * | 1981-09-01 | 1983-03-05 | Kissei Pharmaceut Co Ltd | 核置換シンナモイルアントラニル酸塩およびその製造方法 |
| JPS6019754A (ja) | 1983-07-14 | 1985-01-31 | Kissei Pharmaceut Co Ltd | 芳香族カルボン酸アミド誘導体の製造方法 |
| JPS60152454A (ja) | 1984-01-18 | 1985-08-10 | Terumo Corp | アミド誘導体およびこれを有効成分として含有する５−リポキシゲナ−ゼ作用阻害剤 |
| JPH07116029B2 (ja) * | 1989-04-04 | 1995-12-13 | キッセイ薬品工業株式会社 | トラニラスト水溶液製剤 |
| WO1991012237A1 (en) * | 1990-02-08 | 1991-08-22 | Eisai Co., Ltd. | Benzenesulfonamide derivative |
| US5248825A (en) * | 1990-09-20 | 1993-09-28 | Merrell Dow Pharmaceuticals Inc. | Calcium uptake inhibitors |
| EP0657422B1 (en) * | 1993-12-09 | 1998-06-10 | Ono Pharmaceutical Co., Ltd. | Naphthyloxyacetic acid derivatives as PGE2 agonists and antagonists |
| CN1211182A (zh) | 1996-02-15 | 1999-03-17 | 橘生药品工业株式会社 | 新血管形成抑制剂 |
| JPH09278653A (ja) | 1996-04-05 | 1997-10-28 | Santen Pharmaceut Co Ltd | 網膜疾患治療剤 |
| DE19624155A1 (de) | 1996-06-18 | 1998-01-08 | Hoechst Ag | Substituierte Benzoesäurederivate, Verfahren zu ihrer Herstellung und die Anwendung der Verbindungen zur Behandlung von Krankheiten |
| JPH10259129A (ja) | 1997-01-16 | 1998-09-29 | Kissei Pharmaceut Co Ltd | 血管新生阻害剤 |
| FR2759368B1 (fr) * | 1997-02-10 | 2001-06-01 | Galderma Rech Dermatologique | Composes biaromatiques, compositions les contenant et utilisations |
| JPH10306024A (ja) * | 1997-03-07 | 1998-11-17 | Kissei Pharmaceut Co Ltd | 糸球体疾患の予防および治療剤 |
| JPH10330254A (ja) | 1997-04-01 | 1998-12-15 | Kissei Pharmaceut Co Ltd | 翼状片の進行および術後の再発抑制剤 |
| US6127392A (en) * | 1997-08-05 | 2000-10-03 | American Home Products Corporation | Anthranilic acid analogs |
| DE19935219A1 (de) * | 1999-07-27 | 2001-02-01 | Boehringer Ingelheim Pharma | Carbonsäureamide, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Herstellung |
| ATE479657T1 (de) * | 2001-02-28 | 2010-09-15 | Univ Temple | N-(aryl)-2-arylethensulfonamide und ihre therapeutischen anwendungen |
| US7429593B2 (en) * | 2001-09-14 | 2008-09-30 | Shionogi & Co., Ltd. | Utilities of amide compounds |
| JP4851671B2 (ja) | 2001-10-11 | 2012-01-11 | ニチバン株式会社 | トラニラスト経皮吸収貼付剤およびその製造方法 |
| PL373484A1 (en) | 2001-12-10 | 2005-09-05 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| BR0215240A (pt) * | 2001-12-19 | 2004-10-26 | Atherogenics Inc | Derivados de calcona e seu uso no tratamento de doenças |
| CA2482392A1 (en) * | 2001-12-27 | 2003-07-10 | Taisho Pharmaceutical Co., Ltd. | Carboxylic acid derivative |
| US7351719B2 (en) * | 2002-10-31 | 2008-04-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds |
| DE10254872A1 (de) * | 2002-11-25 | 2004-06-03 | Symrise Gmbh & Co. Kg | Anthranilsäureamide und deren Derivate als kosmetische und pharmazeutische Wirkstoffe |
| US7250444B2 (en) * | 2003-08-11 | 2007-07-31 | Pfizer Inc. | Pyrrole-based HMG-CoA reductase inhibitors |
| GB0319126D0 (en) * | 2003-08-14 | 2003-09-17 | Smithkline Beecham Corp | Chemical compounds |
| DE10346913A1 (de) * | 2003-10-09 | 2005-05-04 | Merck Patent Gmbh | Acylhydrazonderivate |
| US7592373B2 (en) * | 2003-12-23 | 2009-09-22 | Boehringer Ingelheim International Gmbh | Amide compounds with MCH antagonistic activity and medicaments comprising these compounds |
| DE102004030987A1 (de) | 2004-06-26 | 2006-01-12 | Merck Patent Gmbh | Ortho-substituierte (3-Hydroxyphenyl)-essigsäure-benzyliden-hydrazide |
| US7671077B2 (en) * | 2004-07-19 | 2010-03-02 | Leu-Fen Hou Lin | Neuroprotective small organic molecules, compositions and uses related thereto |
| CA2586156A1 (en) * | 2004-11-04 | 2006-05-18 | Merck & Co., Inc. | Niacin receptor agonists, compositions containing such compounds and methods of treatment |
| CA2587407A1 (en) | 2004-11-17 | 2006-05-26 | Angiogen Pharmaceuticals Pty. Ltd. | A method of modulating b cell functioning |
| JP2008520715A (ja) * | 2004-11-23 | 2008-06-19 | メルク エンド カムパニー インコーポレーテッド | ナイアシン受容体アゴニスト、そのような化合物を含む組成物、および治療方法 |
| ITMI20050261A1 (it) * | 2005-02-21 | 2006-08-22 | Carlo Ghisalberti | Analoghi strutturali di avenatramidi loro uso in composizioni utili nel trattamento di disordini dermatologici |
| EP1863756A1 (en) | 2005-03-24 | 2007-12-12 | Janssen Pharmaceutica N.V. | Biaryl derived amide modulators of vanilloid vr1 receptor |
| CA2609059A1 (en) * | 2005-05-16 | 2006-11-23 | Angiogen Pharmaceuticals Pty. Ltd. | Methods and compositions for the treatment of pain |
| WO2006134013A1 (en) | 2005-06-14 | 2006-12-21 | Symrise Gmbh & Co. Kg | Mixtures comprising anthranilic acid amides and cooling agents as cosmetic and pharmaceutical compositions for alleviating itching |
| WO2007015744A1 (en) | 2005-07-21 | 2007-02-08 | Incyte Corporation | Disubstituted thienyl compounds and their use as pharmaceuticals |
| WO2007062957A1 (en) * | 2005-11-30 | 2007-06-07 | Symrise Gmbh & Co. Kg | Mixtures comprising anthranilic acid amides and antidandruff agents as cosmetic and pharmaceutical compositions for alleviating itching |
| US20070286892A1 (en) * | 2006-06-13 | 2007-12-13 | Uri Herzberg | Compositions and methods for preventing or reducing postoperative ileus and gastric stasis in mammals |
| ES2462925T3 (es) * | 2006-06-14 | 2014-05-26 | Symrise Ag | Compuestos con efecto antimicrobiano para el tratamiento de fetidez oral |
| US8765812B2 (en) * | 2006-07-05 | 2014-07-01 | Fibrotech Therapeutics Pty Ltd | Therapeutic compounds |
| KR100832747B1 (ko) | 2006-10-27 | 2008-05-27 | 한국화학연구원 | 아미노피라졸 유도체, 이의 제조 방법 및 이를 함유하는허혈성 질환의 예방 또는 치료용 조성물 |
| US7968577B2 (en) | 2006-11-01 | 2011-06-28 | Bristol-Myers Squibb Company | Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof |
| EP2030617A1 (en) * | 2007-08-17 | 2009-03-04 | Sygnis Bioscience GmbH & Co. KG | Use of tranilast and derivatives thereof for the therapy of neurological conditions |
| US20100292283A1 (en) | 2007-11-28 | 2010-11-18 | Antonio Nardi | Novel phenyl-acetamide and phenyl-propionamide derivatives useful as potassium channel modulators |
| US20090163586A1 (en) | 2007-12-20 | 2009-06-25 | Astrazeneca Ab | Bis-(Sulfonylamino) Derivatives in Therapy 205 |
| JP5730578B2 (ja) | 2007-12-21 | 2015-06-10 | フィブロテック セラピューティクス プロプライエタリー リミテッド | 抗線維症剤のハロゲン化類似体 |
| EP2179984A1 (en) * | 2008-10-27 | 2010-04-28 | Congenia S.r.l. | Acrylamido derivatives useful as inhibitors of the mitochondrial permeability transition |
-
2008
- 2008-12-19 JP JP2010538278A patent/JP5730578B2/ja active Active
- 2008-12-19 AU AU2008341010A patent/AU2008341010B2/en active Active
- 2008-12-19 WO PCT/AU2008/001868 patent/WO2009079692A1/en not_active Ceased
- 2008-12-19 SG SG10201506526QA patent/SG10201506526QA/en unknown
- 2008-12-19 EP EP08865709.3A patent/EP2220028B1/en active Active
- 2008-12-19 KR KR1020167002802A patent/KR20160017139A/ko not_active Ceased
- 2008-12-19 US US12/809,751 patent/US8624056B2/en active Active
- 2008-12-19 MX MX2016000325A patent/MX372721B/es unknown
- 2008-12-19 CN CN2008801221536A patent/CN102164887A/zh active Pending
- 2008-12-19 CN CN201710172053.5A patent/CN107162928B/zh active Active
- 2008-12-19 NZ NZ584613A patent/NZ584613A/en unknown
- 2008-12-19 EP EP16156167.5A patent/EP3045170B1/en active Active
- 2008-12-19 MX MX2010006787A patent/MX337320B/es active IP Right Grant
- 2008-12-19 CA CA2709937A patent/CA2709937C/en active Active
- 2008-12-19 KR KR1020107011284A patent/KR101593708B1/ko active Active
-
2010
- 2010-05-13 ZA ZA2010/03376A patent/ZA201003376B/en unknown
-
2015
- 2015-04-08 JP JP2015079433A patent/JP6063985B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN107162928A (zh) | 2017-09-15 |
| JP6063985B2 (ja) | 2017-01-18 |
| EP3045170A1 (en) | 2016-07-20 |
| AU2008341010A1 (en) | 2009-07-02 |
| MX337320B (es) | 2016-01-06 |
| CA2709937A1 (en) | 2009-07-02 |
| JP5730578B2 (ja) | 2015-06-10 |
| EP2220028A1 (en) | 2010-08-25 |
| EP2220028A4 (en) | 2011-02-16 |
| US8624056B2 (en) | 2014-01-07 |
| EP3045170B1 (en) | 2018-07-04 |
| JP2015180624A (ja) | 2015-10-15 |
| MX2010006787A (es) | 2010-10-04 |
| CN102164887A (zh) | 2011-08-24 |
| EP2220028B1 (en) | 2016-03-09 |
| KR20100099134A (ko) | 2010-09-10 |
| US20110021815A1 (en) | 2011-01-27 |
| CA2709937C (en) | 2016-03-22 |
| NZ584613A (en) | 2011-07-29 |
| WO2009079692A1 (en) | 2009-07-02 |
| SG10201506526QA (en) | 2015-09-29 |
| JP2011506490A (ja) | 2011-03-03 |
| AU2008341010B2 (en) | 2013-04-18 |
| KR101593708B1 (ko) | 2016-02-12 |
| ZA201003376B (en) | 2011-02-23 |
| KR20160017139A (ko) | 2016-02-15 |
| US20120059188A9 (en) | 2012-03-08 |
| CN107162928B (zh) | 2022-03-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX372721B (es) | Ánalogos halogenados de agentes antifi-broticos. | |
| TN2011000279A1 (en) | Novel pyrazole -4-n-alkoxycarboxamides as microbiocides | |
| EA201490912A1 (ru) | Производные [1,2,3]триазоло[4,5-d]пиримидина в качестве агонистов каннабиноидного рецептора 2 | |
| CR11861A (es) | Compuestos organicos | |
| CY1109911T1 (el) | Πυρρολοβενζοδιαζεπινες | |
| MX388468B (es) | Compuestos multicíclicos y métodos de uso de los mismos. | |
| AU2014270524A8 (en) | 2-phenylimidazo [1,2-a]pyrimidines as imaging agents | |
| MX2010008040A (es) | Derivados de pirimidina 5-fluoro como fungicidas. | |
| IL204437A (en) | History of aryl cyclic profile and their use | |
| IN2014MN01640A (enExample) | ||
| MX2010009646A (es) | Agentes terapeuticos antivirales. | |
| UA112428C2 (uk) | Пестицидні композиції і пов'язані з ними способи | |
| EA201270216A1 (ru) | Фармацевтический состав | |
| MX354021B (es) | Derivados de 5-fluor-4-imino-3- (sustituido) -3,4-dihidropirimidin -2 (1h) ona. | |
| UA103625C2 (en) | 5-hetrocyclylalkyl-3-hydroxy-2-phenylcyclopent-2-enons as herbicides | |
| MX2009007713A (es) | Derivados de piridazina, procedimientos para su preparacion y su uso como fungicidas. | |
| PH12014500814A1 (en) | New aryl-quinoline derivatives | |
| UA102289C2 (ru) | Гербициды, полученные из циклопентадиона | |
| MY161132A (en) | Novel herbicides | |
| MX2011007998A (es) | Nuevos herbicidas. | |
| MA38982A1 (fr) | Nouvel octahydro-cyclobuta [1,2-c; 3,4-c'] dipyrrol-2-yl | |
| MX2011007932A (es) | Herbicidas nuevos. | |
| PH12014501026A1 (en) | [1, 2, 3]triazolo[4,5-d] pyrimidine derivatives as agonists of the cannabinoid receptor 2 agonists | |
| UA106880C2 (uk) | Нові гербіциди | |
| TN2011000355A1 (en) | Novel microbiocides |