PE20090361A1 - Acidos benzoilamino-indan-2-carboxilicos sustituidos como inhibidores de cxcr5 - Google Patents
Acidos benzoilamino-indan-2-carboxilicos sustituidos como inhibidores de cxcr5Info
- Publication number
- PE20090361A1 PE20090361A1 PE2008000961A PE2008000961A PE20090361A1 PE 20090361 A1 PE20090361 A1 PE 20090361A1 PE 2008000961 A PE2008000961 A PE 2008000961A PE 2008000961 A PE2008000961 A PE 2008000961A PE 20090361 A1 PE20090361 A1 PE 20090361A1
- Authority
- PE
- Peru
- Prior art keywords
- benzoylamine
- indan
- halogen
- alkyl
- cxcr5
- Prior art date
Links
- 239000002253 acid Substances 0.000 title abstract 3
- 102100031658 C-X-C chemokine receptor type 5 Human genes 0.000 title abstract 2
- 101000922405 Homo sapiens C-X-C chemokine receptor type 5 Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000007513 acids Chemical group 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- -1 CARBOXYL Chemical class 0.000 abstract 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- NFQUEVQQAVDQPM-UHFFFAOYSA-N 3-methyl-2-prop-2-enoxybenzamide Chemical compound CC1=CC=CC(C(N)=O)=C1OCC=C NFQUEVQQAVDQPM-UHFFFAOYSA-N 0.000 abstract 1
- WFLZGFARTOLXKH-UHFFFAOYSA-N 3-methyl-2-propan-2-yloxybenzamide Chemical compound CC(C)OC1=C(C)C=CC=C1C(N)=O WFLZGFARTOLXKH-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 206010025135 lupus erythematosus Diseases 0.000 abstract 1
- 201000006417 multiple sclerosis Diseases 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/78—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P19/00—Drugs for skeletal disorders
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- A—HUMAN NECESSITIES
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- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
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- 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]
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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
- C07C233/52—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 a carbon atom of a ring other than a six-membered aromatic ring
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- 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
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- C07C235/54—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07C255/11—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound oxygen atoms bound to the same saturated acyclic carbon skeleton
- C07C255/13—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound oxygen atoms bound to the same saturated acyclic carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring
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Abstract
REFERIDA A UN DERIVADO CARBOXILICO DE FORMULA (Ia), DONDE A ES CH=CH O S; R23 ES H, HALOGENO, ALUILO C1-C4, ALQUILOXI C1-C4, ALQUILO C1-C4-S O NITRO; R24 ES H, HALOGENO, ALQUILO C1-C4, ENTRE OTROS; X ES N(H)C=O, N(H)S(O)2, C(=O)N(H), S(O)2N(H); Y ES N(R11), S, O, C(R12)=C(R13), ENTRE OTROS; R11 ES H, ALQUILO C1-C10, ALQUILOXI C1-C10, ENTRE OTROS; R12 ES H, HALOGENO, ALQUILO C1-C10, ALQUENILO C2-C10, ENTRE OTROS; R13 ES H, HALOGENO, ENTRE OTROS; R21 ES H, ALQUILO C1-C4, ALQUILOXI C1-C3, HALOGENO, ENTRE OTROS; R22 ES H, HALOGENO, CN, NITRO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ACIDO 2-(2-ALILOXI-3-METIL-BENZOILAMINO)-INDAN-2-CARBOXILICO, ACIDO 2-(2-ISOPROPOXI-3-METIL-BENZOILAMINO)-INDAN-2-CARBOXILICO, ACIDO 2-(2-CICLOBUTOXI-3-METIL-BENZOILAMINO)-INDAN-2-CARBOXILICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS TIENEN ACTIVIDAD INHIBIDORA DEL RECEPTOR CXCR5 Y SON UTILES EN EL TRATAMIENTO DE ARTRITIS REUMATOIDE, ESCLEROSIS MULTIPLE, LUPUS, ENTRE OTROS
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| JP5674463B2 (ja) | 2007-06-05 | 2015-02-25 | サノフイ | 置換されたベンゾイルアミノ−インダン−2−カルボン酸及び関連化合物 |
| CA2723302C (en) * | 2008-05-05 | 2013-08-20 | Sanofi-Aventis | Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals |
| AR074760A1 (es) | 2008-12-18 | 2011-02-09 | Metabolex Inc | Agonistas del receptor gpr120 y usos de los mismos en medicamentos para el tratamiento de diabetes y el sindrome metabolico. |
| EP2316818A1 (en) * | 2009-11-03 | 2011-05-04 | Active Biotech AB | Method for the preparation of 2-amino-6-ethylbenzoic acid |
| CN101735041B (zh) * | 2009-12-17 | 2013-06-12 | 太仓市运通化工厂 | 一种邻羧基苯甲醛的制备方法 |
| DK2582674T3 (en) * | 2010-06-16 | 2014-12-15 | Cymabay Therapeutics Inc | GPR120 receptor agonists and uses thereof. |
| US8299117B2 (en) | 2010-06-16 | 2012-10-30 | Metabolex Inc. | GPR120 receptor agonists and uses thereof |
| CA2852160A1 (en) | 2011-10-28 | 2013-05-02 | Galderma Research & Development | New leukocyte infiltrate markers for rosacea and uses thereof |
| WO2014003744A1 (en) * | 2012-06-27 | 2014-01-03 | Morehouse School Of Medicine | Anti-cxcl9, anti-cxcl 10, anti-cxcl 11, anti-cxcl 13, anti-cxcr3 and anti-cxcr5 agents for inflammatory disorder |
| RS62639B1 (sr) | 2015-07-06 | 2021-12-31 | Alkermes Inc | Hetero-halo inhibitori histonskih deacetilaza |
| EP3319968A1 (en) | 2015-07-06 | 2018-05-16 | Rodin Therapeutics, Inc. | Heterobicyclic n-aminophenyl-amides as inhibitors of histone deacetylase |
| GB201615191D0 (en) * | 2016-09-07 | 2016-10-19 | Takeda Pharmaceuticals Co | Novel compounds |
| TWI770104B (zh) | 2017-01-11 | 2022-07-11 | 美商羅登醫療公司 | 組蛋白去乙醯酶雙環抑制劑 |
| GB201704476D0 (en) | 2017-03-21 | 2017-05-03 | Antabio Sas | Chemical compounds |
| PL3664802T3 (pl) | 2017-08-07 | 2022-07-11 | Alkermes, Inc. | Bicykliczne inhibitory deacetylaz histonowych |
| SMT202200134T1 (it) | 2018-03-08 | 2022-05-12 | Incyte Corp | Composti di amminopirazindiolo come inibitori di pi3k-y |
| WO2020010003A1 (en) | 2018-07-02 | 2020-01-09 | Incyte Corporation | AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS |
| EP3628666A1 (en) | 2018-09-25 | 2020-04-01 | Antabio SAS | Indane derivatives for use in the treatment of bacterial infection |
| MX2021003498A (es) | 2018-09-25 | 2021-09-10 | Antabio Sas | Derivados de indano para el uso en el tratamiento de infeccion bacteriana. |
| EP3628672A1 (en) | 2018-09-25 | 2020-04-01 | Antabio SAS | Indane derivatives for use in the treatment of bacterial infection |
| WO2020064175A1 (en) | 2018-09-25 | 2020-04-02 | Antabio Sas | Indane derivatives for use in the treatment of bacterial infection |
| MX2021003750A (es) * | 2018-10-11 | 2021-06-15 | Basf As | Compuestos aromaticos y usos farmaceuticos de los mismos. |
| CN110938015B (zh) * | 2019-12-06 | 2022-10-25 | 重庆工商大学 | 一种叠氮基取代的水杨酸衍生物的制备方法 |
| US20240016941A1 (en) | 2020-03-24 | 2024-01-18 | Antabio Sas | Combination therapy |
| US12414927B2 (en) | 2020-03-31 | 2025-09-16 | Yale University | CXCR5 antagonists and methods of treating diseases or disorders using same |
| JP2023538713A (ja) | 2020-05-06 | 2023-09-11 | バイエル、アクチエンゲゼルシャフト | 殺真菌性化合物としてのピリジン(チオ)アミド |
| US20230295138A1 (en) | 2020-06-04 | 2023-09-21 | Bayer Aktiengesellschaft | Heterocyclyl pyridines as novel fungicides |
| WO2023042314A1 (ja) * | 2021-09-15 | 2023-03-23 | 和幸 吉崎 | 免疫異常性炎症性疾患を治療または予防するための組成物 |
| CN118317956A (zh) | 2021-11-30 | 2024-07-09 | 拜耳公司 | 作为杀真菌化合物的双(杂)芳基硫醚噁二嗪 |
| CN116217415B (zh) * | 2023-02-13 | 2024-06-18 | 武汉大学 | 一种合成手性3-氨基-1-苯基丙醇和手性3-(甲氨基)-1-苯基丙醇的方法 |
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| FR2701480B1 (fr) * | 1993-02-15 | 1995-05-24 | Sanofi Elf | Composés à groupe sulfamoyle et amidino, leur procédé de préparation et les compositions pharmaceutiques les contenant. |
| HUP0000852A2 (hu) * | 1997-02-03 | 2001-05-28 | Pfizer Products Inc. | Aril-szulfonil-amino-hidroxámsav-származékok, valamint e vegyületeket tartalmazó gyógyászati készítmények |
| US5932765A (en) * | 1997-05-23 | 1999-08-03 | Merck Patent Gesellschaft Mit | Nitromethyl ketones, process for preparing them and compositions containing them |
| EP0998282A4 (en) * | 1997-05-29 | 2000-08-30 | Merck & Co Inc | SULPHONAMIDES AS CELL ADHESION INHIBITORS |
| EP1009737A2 (en) * | 1997-07-31 | 2000-06-21 | The Procter & Gamble Company | Sulfonylamino substituted hydroxamic acid derivatives as metalloprotease inhibitors |
| US6929928B2 (en) * | 2003-06-12 | 2005-08-16 | E. I. Du Pont De Nemours And Company | Genes encoding carotenoid compounds |
| US20090018145A1 (en) * | 2004-10-19 | 2009-01-15 | Compass Pharmaceuticals Llc | Compositions and their use as anti-tumor agents |
| EP1676834A1 (en) * | 2004-12-30 | 2006-07-05 | Sanofi-Aventis Deutschland GmbH | Fused bicyclic carboxamide derivates for use as CXCR2 inhibitors in the treatment of inflammation |
| EP1849465A4 (en) * | 2005-02-18 | 2008-12-24 | Takeda Pharmaceutical | AGENS TO CONTROL THE FUNCTION OF THE GPR34 RECEPTOR |
| JP5232144B2 (ja) * | 2006-06-28 | 2013-07-10 | サノフイ | Cxcr2阻害剤 |
| JP5237938B2 (ja) * | 2006-06-28 | 2013-07-17 | サノフイ | 新規なcxcr2阻害剤 |
| WO2008036967A2 (en) * | 2006-09-22 | 2008-03-27 | Reddy Us Therapeutics, Inc. | Novel heterocyclic compounds as lasy activators |
| JP5674463B2 (ja) | 2007-06-05 | 2015-02-25 | サノフイ | 置換されたベンゾイルアミノ−インダン−2−カルボン酸及び関連化合物 |
| CA2723302C (en) * | 2008-05-05 | 2013-08-20 | Sanofi-Aventis | Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals |
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