AR070649A1 - Derivados de 1,3- dihidro -isoindol - Google Patents
Derivados de 1,3- dihidro -isoindolInfo
- Publication number
- AR070649A1 AR070649A1 ARP080103758A ARP080103758A AR070649A1 AR 070649 A1 AR070649 A1 AR 070649A1 AR P080103758 A ARP080103758 A AR P080103758A AR P080103758 A ARP080103758 A AR P080103758A AR 070649 A1 AR070649 A1 AR 070649A1
- Authority
- AR
- Argentina
- Prior art keywords
- hal
- atoms
- replaced
- mono
- nr6conr6r7
- Prior art date
Links
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical class C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 title abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 2
- 101710113864 Heat shock protein 90 Proteins 0.000 abstract 2
- 102100034051 Heat shock protein HSP 90-alpha Human genes 0.000 abstract 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 1
- 240000000543 Pentas lanceolata Species 0.000 abstract 1
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 230000033228 biological regulation Effects 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000000565 sulfonamide group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
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- Pharmacology & Pharmacy (AREA)
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Abstract
Los derivados de 1,3-dihidro-isoindol de la formula (1) en donde R1 es A; R2 es A, (CH2)nAr o (CH2)nHet; R1 y R2 son, junto con el átomo de N al que están unidos, isoindolilo; R3 es H, Hal, OH, CN, NO2, C(O)H, NH2, COOH, COOA, CsCH, CsC-CH2OH, CONH2, CONHA, CONAA', SO2NH2, NHCONH2, X-A, X-(CH2)nAr o X-(CH2)nHet, en donde X es un enlace, -O-, -CO-, -CO2-, -C(O)NH, -C(O)NA', -S-, -SO-, -SO2-, SO2NH-, -SO2NA', -NH-, -NA'-, -NHSO2-, -NA'SO2, -NHCO-, -NA'CO-, -NHCONH- o -NA'CONH-; R3' es H, A, Hal, OA o CN; A, A' son en cada caso, de modo independiente entre sí, alquilo no ramificado o ramificado C1-10, en donde uno, dos o tres grupos CH2 o CH no adyacentes pueden estar reemplazados por O, S, SO, SO2, CO, NH, NR5 y/o por grupos -CH=CH y/o también 1-5 átomos de H pueden estar reemplazados por F, Cl, Br y/o R4, o cicloalquilo C3-7, A y A' son, junto con el átomo de N al que están unidos, también un heterociclo monocíclico saturado no sustituido o mono-, di- o trisustituido con Hal, A, (CH2)nOH, (CH2)nOA y/u =O (oxígeno del carbonilo), que puede contener otros 1 a 3 átomos de N, O y/o S; R4 es COOR6, CN, CONR6R7, NR6R7, NHCOR6, NHCOOR6, NR6CONR6R7 u OR6; R5 es cicloalquilo C3-7, cicloalquilalquileno C4-10, Alk o alquilo no ramificado o ramificado C1-6, en donde uno, dos o tres grupos CH2 o CH no adyacentes pueden estar reemplazados por O, CO, S, SO, SO2, NH y/o también 1-5 átomos de H pueden estar reemplazados por F y/o Cl; R6, R7 son en cada caso, de modo independiente entre sí, H o alquilo C1-5, en donde 1-3 grupos CH2 o CH no adyacentes pueden estar reemplazados por O, CO, S, SO, SO2, NH, NMe o Net y/o también 1-5 átomos de H pueden estar reemplazados por F y/o Cl, R6 y R7 son juntos también una cadena de alquileno con 2, 3, 4, 5 o 6 átomos de C, en donde 1-3 átomos de C no adyacentes pueden estar reemplazados por O, CO, S, SO, SO2, NH, NR5, NCOR5 o NCOOR5; Alk es alquenilo C2-6; Ar es fenilo, naftilo o bifenilo no sustituido o mono-, di-, tri-, tetra o pentasustituido con Hal, A, (CH2)nCN, (CH2)nAr', (CH2)nHet', (CH2)nOA, (CH2)nOH, S(O)mA, NO2, (CH2)NR6R7, NR5R6, CONR6R7 CONR5R6, SO2NR6R7, SO2NR5R6, NR6COR7, NR6CONR6R7 y/o NR6SO2R7; Ar' es fenilo, naftilo o bifenilo no sustituido o mono-, di- o trisustituido con Hal, A, CN, fenilo, OA, OH, S(O)mA, NO2, NR6R7, NR5R6, CONR6R7, CONR5R6, SO2NR6R7, SO2NR5R6, NR6COR7, NR6CONR6R7 y/o NR6SO2R7; Het es un heterociclo saturado, insaturado o aromático mono- o bicíclico con 1 a 4 átomos de N, O y/o S, que puede no estar sustituido o que puede estar mono-, di- o trisustituido con Hal, A, CN, Ar', Het' OA, OH, S(O)mA, NO2, NR6R7, NR5R6, CONR6R7, CONR5R6, SO2NR6R7, SO2NR5R6, NR6COR7, NR6CONR6R7, NR6SO2R7, =S, =NR8, =NR8R4 y/u =O (oxígeno del carbonilo); Het' es un heterociclo saturado, insaturado o aromático mono- o bicíclico con 1 a 4 átomos de N, O y/o S, que puede no estar sustituido o que puede estar mono-, di- o trisustituido con Hal, A, CN, Ar', OA, OH, S(O)nA, NO2, NR6R7, NR5R6, CONR6R7, CONR5R6, SO2NR6R7, SO2NR5R6, NR6COR7, NR6CONR6R7, NR6SO2R7, =S, =NR8, =NR8R4 y/u =O (oxígeno del carbonilo); R8 es H o A; Hal es F, Cl, Br o I; m es 0, 1 o 2, n 0, 1, 2, 3 o 4; así como sus derivados, sales, solvatos y estereoisomeros de utilidad farmacéutica, incluyendo sus mezclas en todas las proporciones. Son inhibidores de la HSP90 y pueden ser utilizados para preparar un medicamento para el tratamiento de enfermedades en las que la inhibicion, la regulacion y/o la modulacion de la HSP90 desempena un papel importante.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007041116A DE102007041116A1 (de) | 2007-08-30 | 2007-08-30 | 1,3-Dihydro-isoindolderivate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR070649A1 true AR070649A1 (es) | 2010-04-28 |
Family
ID=40029128
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080103758A AR070649A1 (es) | 2007-08-30 | 2008-08-29 | Derivados de 1,3- dihidro -isoindol |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8183279B2 (es) |
| EP (1) | EP2181092B1 (es) |
| JP (1) | JP5529739B2 (es) |
| KR (1) | KR20100061817A (es) |
| CN (1) | CN101790513A (es) |
| AR (1) | AR070649A1 (es) |
| AU (1) | AU2008295176B2 (es) |
| BR (1) | BRPI0815059A2 (es) |
| CA (1) | CA2697934C (es) |
| DE (1) | DE102007041116A1 (es) |
| EA (1) | EA201000362A1 (es) |
| ES (1) | ES2532853T3 (es) |
| IL (1) | IL204126A (es) |
| MX (1) | MX2010002042A (es) |
| WO (1) | WO2009030316A1 (es) |
| ZA (1) | ZA201002217B (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2949467B1 (fr) | 2009-09-03 | 2011-11-25 | Sanofi Aventis | Nouveaux derives de 5,6,7,8-tetrahydroindolizine inhibiteurs d'hsp90, compositions les contenant et utilisation |
| MX2014014188A (es) | 2012-05-25 | 2015-05-11 | Berg Llc | Metodos para tratar un sindrome metaboilico mediante la modulacion de la proteina de choque termico (hsp) 90-beta. |
| HK1217649A1 (zh) * | 2012-12-27 | 2017-01-20 | 德雷克塞尔大学 | 針對hbv感染的新型抗病毒劑 |
| WO2015188198A2 (en) | 2014-06-06 | 2015-12-10 | Berg Llc | Methods of treating a metabolic syndrome by modulating heat shock protein (hsp) 90-beta |
| SG11201610746SA (en) * | 2014-07-08 | 2017-01-27 | Viiv Healthcare Uk Ltd | Isoindoline derivatives for use in the treatment of a viral infection |
| US10316167B2 (en) | 2014-09-19 | 2019-06-11 | Plastipak Packaging | Oxygen scavengers, compositions comprising the scavengers, and articles made from the compositions |
| US10464907B2 (en) * | 2016-01-29 | 2019-11-05 | Industry Academic Cooperation Foundation Keimyung University | Compound having HSP90 inhibitory activity or pharmaceutically acceptable salt thereof, and medical use thereof |
| EP3478686B1 (en) | 2016-06-29 | 2020-04-15 | H. Hoffnabb-La Roche Ag | Novel dihydropyrrolopyrimidines for the treatment and prophylaxis of hepatitis b virus infection |
| CN106366089B (zh) * | 2016-08-19 | 2019-06-11 | 爱斯特(成都)生物制药股份有限公司 | 二氢异吲哚衍生物及其类似物的制备方法 |
| WO2018132769A1 (en) | 2017-01-12 | 2018-07-19 | University Of Kansas | Hsp90b n-terminal isoform-selective inhibitors |
| EP4573087A1 (en) * | 2022-08-21 | 2025-06-25 | University of Notre Dame du Lac | Use of (isoindolin-2-yl)(4-hydroxy-3-(isoindoline-2-carbonyl)phenyl)methanones in the treatment of tumor necrosis factor receptor-associated protein 1 dysfunction |
| CN117402075B (zh) * | 2023-10-17 | 2026-01-09 | 厦门大学深圳研究院 | 一种具有特异性抗肿瘤活性的可见光响应的人工h+/ci-离子通道的制备 |
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| US5968921A (en) | 1997-10-24 | 1999-10-19 | Orgegon Health Sciences University | Compositions and methods for promoting nerve regeneration |
| AU3378599A (en) | 1998-04-03 | 1999-10-25 | University Of Pittsburgh | Benzoquinoid ansamycins for the treatment of cardiac arrest and stroke |
| CA2367108A1 (en) | 1999-03-12 | 2000-09-14 | The United States Of America, Represented By The Secretary, Department O F Health And Human Services | Method of inhibiting a chaperone protein |
| EP1265913A4 (en) | 2000-03-24 | 2004-07-14 | Univ Duke | CHARACTERIZATION OF THE INTERACTION BETWEEN GRP94 AND A LIGAND, AND CLEANING, SCREENING AND THERAPEUTIC PROCEDURES RELATING TO IT |
| WO2002002123A1 (en) | 2000-06-29 | 2002-01-10 | Trustees Of Boston University | Use of geldanamycin and related compounds for prophylaxis or treatment of fibrogenic disorders |
| EP1322325A4 (en) | 2000-07-20 | 2004-09-15 | Merck & Co Inc | INHIBITION OF PROCESSING AND REPLICATION OF HEPATITIS C VIRUS |
| WO2002009696A1 (en) | 2000-07-28 | 2002-02-07 | Sloan-Kettering Institute For Cancer Research | Methods for treating cell proliferative disorders and viral infections |
| CA2440842A1 (en) | 2001-04-16 | 2002-10-24 | Eisai Co., Ltd. | Novel 1h-indazole compounds |
| AU2002356922A1 (en) | 2001-11-09 | 2003-05-26 | Conforma Therapeutics Corporation | Hsp90-inhibiting zearalanol compounds and methods of producing and using same |
| BRPI0513819A (pt) | 2004-07-27 | 2008-05-20 | Novartis Ag | inibidores de hsp90 |
| WO2006109075A2 (en) * | 2005-04-13 | 2006-10-19 | Astex Therapeutics Limited | Hydroxybenzamide derivatives and their use as inhibitors of hsp90 |
| CA2605985A1 (en) | 2005-05-03 | 2006-11-09 | Pfizer Inc. | Amide resorcinol compounds |
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- 2008-07-28 KR KR1020107006638A patent/KR20100061817A/ko not_active Withdrawn
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| JP2010536893A (ja) | 2010-12-02 |
| MX2010002042A (es) | 2010-03-15 |
| EP2181092B1 (de) | 2015-01-14 |
| CN101790513A (zh) | 2010-07-28 |
| CA2697934C (en) | 2016-02-16 |
| AU2008295176A1 (en) | 2009-03-12 |
| JP5529739B2 (ja) | 2014-06-25 |
| AU2008295176B2 (en) | 2013-05-02 |
| US20100311745A1 (en) | 2010-12-09 |
| EP2181092A1 (de) | 2010-05-05 |
| IL204126A (en) | 2015-07-30 |
| WO2009030316A1 (de) | 2009-03-12 |
| KR20100061817A (ko) | 2010-06-09 |
| US8183279B2 (en) | 2012-05-22 |
| ZA201002217B (en) | 2017-11-29 |
| CA2697934A1 (en) | 2009-03-12 |
| DE102007041116A1 (de) | 2009-03-05 |
| EA201000362A1 (ru) | 2010-08-30 |
| ES2532853T3 (es) | 2015-04-01 |
| BRPI0815059A2 (pt) | 2015-02-10 |
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