ZA200704789B - Novel anthranilic acid derivative or salt thereof - Google Patents
Novel anthranilic acid derivative or salt thereofInfo
- Publication number
- ZA200704789B ZA200704789B ZA200704789A ZA200704789A ZA200704789B ZA 200704789 B ZA200704789 B ZA 200704789B ZA 200704789 A ZA200704789 A ZA 200704789A ZA 200704789 A ZA200704789 A ZA 200704789A ZA 200704789 B ZA200704789 B ZA 200704789B
- Authority
- ZA
- South Africa
- Prior art keywords
- salt
- acid derivative
- anthranilic acid
- novel anthranilic
- novel
- Prior art date
Links
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 title 1
- 150000003839 salts Chemical class 0.000 title 1
Classifications
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- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/82—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/87—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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- C07C229/46—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C229/48—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms of the same non-condensed ring
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- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
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- C07C233/51—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
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- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
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- C07D207/325—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- C07D207/416—2,5-Pyrrolidine-diones 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 other ring carbon atoms
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- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Indole Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pyrrole Compounds (AREA)
Applications Claiming Priority (1)
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JP2004353725 | 2004-12-07 |
Publications (1)
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ZA200704789B true ZA200704789B (en) | 2008-11-26 |
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ZA200704789A ZA200704789B (en) | 2004-12-07 | 2005-12-06 | Novel anthranilic acid derivative or salt thereof |
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US (1) | US7999132B2 (ko) |
EP (1) | EP1820795A4 (ko) |
JP (1) | JP4956194B2 (ko) |
KR (1) | KR20070100888A (ko) |
CN (1) | CN101094829B (ko) |
AU (1) | AU2005312721B9 (ko) |
BR (1) | BRPI0518467A2 (ko) |
CA (1) | CA2588633A1 (ko) |
MX (1) | MX2007006790A (ko) |
NO (1) | NO20072605L (ko) |
NZ (1) | NZ555326A (ko) |
RU (1) | RU2394021C2 (ko) |
WO (1) | WO2006062093A1 (ko) |
ZA (1) | ZA200704789B (ko) |
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JP5193861B2 (ja) * | 2005-07-07 | 2013-05-08 | アボット・ラボラトリーズ | アポトーシス促進剤 |
TWI444379B (zh) * | 2007-06-29 | 2014-07-11 | Sunesis Pharmaceuticals Inc | 有用於作為Raf激酶抑制劑之化合物 |
CN101412682B (zh) * | 2007-10-19 | 2012-06-27 | 上海药明康德新药开发有限公司 | 芳基氨茴酸及其衍生物的合成方法 |
BRPI0817897A2 (pt) * | 2007-11-02 | 2019-09-24 | Methylgene Inc | composto, composição, e, métodos de inibição da atividade hdac, e de tratamento de uma doença responsiva a um inibidor de atividade hdac |
BRPI0916576A2 (pt) | 2008-08-04 | 2017-06-27 | Chdi Inc | pelo menos uma entidade química, composição farmacêutica, e, método para tratar uma condição ou distúrbio. |
CN102170882B (zh) * | 2008-08-29 | 2014-04-02 | 特温蒂斯公司 | 治疗淀粉状蛋白疾病的组合物和其制药用途 |
EP2340243B1 (en) | 2008-10-17 | 2014-10-08 | Boehringer Ingelheim International GmbH | Heteroaryl substituted indole compounds useful as mmp-13 inhibitors |
RU2529860C2 (ru) * | 2009-01-30 | 2014-10-10 | Тояма Кемикал Ко., Лтд. | Производное n-ацилантраниловой кислоты или его соль |
JP5730190B2 (ja) | 2009-03-31 | 2015-06-03 | 株式会社レナサイエンス | プラスミノーゲンアクチベーターインヒビター−1阻害剤 |
WO2011056985A2 (en) * | 2009-11-04 | 2011-05-12 | Gilead Sciences, Inc. | Substituted heterocyclic compounds |
EP2528441A4 (en) | 2010-01-25 | 2013-07-10 | Chdi Foundation Inc | CERTAIN KYNURENIN-3-MONOOXYGENASE INHIBITORS, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF |
EP2550253B9 (en) * | 2010-03-22 | 2016-09-21 | Rensselaer Polytechnic Institute | Morphinane derivatives containing a carboxamide group as opioid receptor ligands |
EP2714941A4 (en) * | 2011-05-24 | 2014-12-03 | Wistar Inst | COMPOSITIONS AND METHODS FOR MODULATING THE EFFECT OF THE EPSTEIN-BARR NUCLEAR ANTIGEN 1 |
SG2014011654A (en) | 2011-08-30 | 2014-08-28 | Chdi Foundation Inc | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
AU2012302144B2 (en) | 2011-08-30 | 2017-06-15 | Chdi Foundation, Inc. | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
US9730913B2 (en) * | 2011-10-13 | 2017-08-15 | The Johns Hopkins University | High affinity beta lactamase inhibitors |
WO2014151953A1 (en) | 2013-03-15 | 2014-09-25 | The California Institute For Biomedical Research | Compounds and methods for inducing chondrogenesis |
US10092537B2 (en) | 2013-04-15 | 2018-10-09 | Renascience Co., Ltd. | Use for PAI-1 inhibitor |
WO2014170706A1 (en) * | 2013-04-15 | 2014-10-23 | Università Degli Studi Di Bari | Galloyl benzamide-based compounds as jnk modulators |
GB201322538D0 (en) | 2013-06-21 | 2014-02-05 | Immusmol Sas | Method for detecting small molecules in a sample |
MX2016011468A (es) * | 2014-03-07 | 2017-01-23 | Biocryst Pharm Inc | Inhibidores de calicreína plasmática humana. |
CA2955379C (en) | 2014-07-17 | 2022-12-13 | Chdi Foundation, Inc. | Methods and compositions for treating hiv-related disorders |
WO2016027282A1 (en) * | 2014-08-20 | 2016-02-25 | Council Of Scientific & Industrial Research | N-((3,4,5-trimethoxystyryl)aryl)cinnamamide compounds as potential anticancer agents and process for the preparation thereof |
ES2578377B1 (es) * | 2014-12-22 | 2017-05-04 | Consejo Superior De Investigaciones Científicas (Csic) | Compuestos moduladores del sensor neuronal de calcio dream y sus usos terapéuticos. |
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 |
WO2018157801A1 (zh) * | 2017-02-28 | 2018-09-07 | 广东东阳光药业有限公司 | 氰基取代的稠合双环衍生物及其制备方法和用途 |
IT201700028127A1 (it) | 2017-03-14 | 2018-09-14 | Fondazione St Italiano Tecnologia | Composti e composizioni per il trattamento della fibrosi cistica |
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 |
BR112020026148A2 (pt) * | 2018-06-21 | 2021-03-16 | Cellestia Biotech Ag | Processo para fabricar éteres amino diarílicos e sais de cloridratos de éteres amino diarílicos |
AU2020332005B2 (en) * | 2019-08-21 | 2024-05-23 | The Scripps Research Institute | Monocyclic agonists of stimulator of interferon genes sting |
WO2022006534A1 (en) * | 2020-07-02 | 2022-01-06 | The Brigham And Women's Hospital, Inc. | Targeting serpin b9 in cancer |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
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DE2331444A1 (de) * | 1973-06-20 | 1975-01-23 | Hoechst Ag | Neue styryl-benzoxazole, verfahren zu deren herstellung und ihre verwendung als optische aufhellungsmittel |
JP2000515153A (ja) * | 1996-07-22 | 2000-11-14 | モンサント カンパニー | チオールスルホンアミド メタロプロテアーゼインヒビター |
CA2337098C (en) | 1998-07-24 | 2008-08-05 | Teijin Limited | Anthranilic acid derivatives |
PL360678A1 (en) * | 2000-03-17 | 2004-09-20 | Bristol-Myers Squibb Pharma Company | Cyclic beta-amino acid derivatives as inhibitors of matrix metalloproteases and tnf-alpha |
DE10065042A1 (de) * | 2000-12-23 | 2002-06-27 | Boehringer Ingelheim Pharma | Carbonsäureamide, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Herstellung |
PA8539301A1 (es) * | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Inhibidores de la metaloproteinasa de la matriz |
DOP2002000333A (es) * | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Derivados de acido isoftalico como inhibidores de metaloproteinasas de la matriz |
GB0126902D0 (en) | 2001-11-08 | 2002-01-02 | Novartis Ag | Organic compounds |
US20060106048A1 (en) * | 2002-07-26 | 2006-05-18 | Yoshihisa Inoue | Furoisoquinoline derivative and use thereof |
SE0400234D0 (sv) * | 2004-02-06 | 2004-02-06 | Active Biotech Ab | New compounds, methods for their preparation and use thereof |
-
2005
- 2005-12-06 US US11/721,007 patent/US7999132B2/en not_active Expired - Fee Related
- 2005-12-06 CN CN2005800457815A patent/CN101094829B/zh not_active Expired - Fee Related
- 2005-12-06 RU RU2007125726/04A patent/RU2394021C2/ru not_active IP Right Cessation
- 2005-12-06 WO PCT/JP2005/022367 patent/WO2006062093A1/ja active Application Filing
- 2005-12-06 BR BRPI0518467-3A patent/BRPI0518467A2/pt not_active IP Right Cessation
- 2005-12-06 MX MX2007006790A patent/MX2007006790A/es active IP Right Grant
- 2005-12-06 CA CA002588633A patent/CA2588633A1/en not_active Abandoned
- 2005-12-06 KR KR1020077015347A patent/KR20070100888A/ko active IP Right Grant
- 2005-12-06 AU AU2005312721A patent/AU2005312721B9/en not_active Ceased
- 2005-12-06 NZ NZ555326A patent/NZ555326A/en not_active IP Right Cessation
- 2005-12-06 ZA ZA200704789A patent/ZA200704789B/xx unknown
- 2005-12-06 JP JP2006546701A patent/JP4956194B2/ja not_active Expired - Fee Related
- 2005-12-06 EP EP05814561A patent/EP1820795A4/en not_active Withdrawn
-
2007
- 2007-05-24 NO NO20072605A patent/NO20072605L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
US20090240052A1 (en) | 2009-09-24 |
EP1820795A4 (en) | 2010-10-20 |
CA2588633A1 (en) | 2006-06-15 |
CN101094829B (zh) | 2012-02-08 |
MX2007006790A (es) | 2007-08-15 |
NO20072605L (no) | 2007-09-05 |
NZ555326A (en) | 2010-01-29 |
BRPI0518467A2 (pt) | 2008-11-18 |
AU2005312721A1 (en) | 2006-06-15 |
JP4956194B2 (ja) | 2012-06-20 |
RU2007125726A (ru) | 2009-01-20 |
KR20070100888A (ko) | 2007-10-12 |
CN101094829A (zh) | 2007-12-26 |
AU2005312721B9 (en) | 2012-08-02 |
US7999132B2 (en) | 2011-08-16 |
EP1820795A1 (en) | 2007-08-22 |
JPWO2006062093A1 (ja) | 2008-06-12 |
RU2394021C2 (ru) | 2010-07-10 |
WO2006062093A1 (ja) | 2006-06-15 |
AU2005312721B2 (en) | 2011-09-08 |
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