AR073898A1 - Compuestos de espiro-oxindol y su uso como agentes terapeuticos. - Google Patents
Compuestos de espiro-oxindol y su uso como agentes terapeuticos.Info
- Publication number
- AR073898A1 AR073898A1 ARP090104002A ARP090104002A AR073898A1 AR 073898 A1 AR073898 A1 AR 073898A1 AR P090104002 A ARP090104002 A AR P090104002A AR P090104002 A ARP090104002 A AR P090104002A AR 073898 A1 AR073898 A1 AR 073898A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- group
- hydrogen
- aralkyl
- chain
- Prior art date
Links
- 239000003814 drug Substances 0.000 title 1
- 229940124597 therapeutic agent Drugs 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 2
- 229910003849 O-Si Inorganic materials 0.000 abstract 1
- 229910003872 O—Si Inorganic materials 0.000 abstract 1
- 108010052164 Sodium Channels Proteins 0.000 abstract 1
- 102000018674 Sodium Channels Human genes 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/20—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
Compuestos para el tratamiento y/o prevencion de enfermedades o afecciones mediadas por canales de sodio, tal como el dolor. Reivindicacion 1: Un compuesto caracterizado porque es de formula (1), donde: n es 0, 1, 2, 3 o 4; R1 se selecciona entre el grupo que consiste de hidrogeno, -R5-C(=NOR6)N(R7)R8, difenilmetilo, aralquilo (opcionalmente sustituido con un sustituyente seleccionado entre el grupo que consiste de -N(R7)R8, - C(=NOR6)N(R7)R8, -O-R5-OR7, -O-R5-C(O)OR7, -O-R5-C(O)N(R7)R8, -O-R5-N(R7)R8 y -S(O)R7 y heterociclilalquilo (opcionalmente sustituido con -C(O)R7; R2 es hidrogeno; R3 se selecciona entre el grupo que consiste de -O-R5-N(R7)R8, -O-R5-N(R7)C(O)OR8, -O-R5-C(O)OR7, -O-Si(R7)3 y -N[S(O)2R7]2; o R2 y R3, junto con los carbonos a los cuales se encuentran unidos, formar un anillo O-heterociclilo opcionalmente sustituido con =NOR7; R4 se selecciona entre el grupo que consiste de alquilo, halo, haloalquilo, arilo opcionalmente sustituido y aralquilo opcionalmente sustituido; cada R5 se selecciona independientemente entre el grupo que consiste de una cadena alquileno lineal o ramificada opcionalmente sustituida, una cadena alquenileno lineal o ramificada opcionalmente sustituida y una cadena alquinileno lineal o ramificada opcionalmente sustituida; R6 se selecciona entre el grupo que consiste de hidrogeno y -C(O)R7; y cada R7 y R8 se selecciona independientemente entre el grupo que consiste de hidrogeno, alquilo, haloalquilo, arilo opcionalmente sustituido, aralquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido, cicloalquilalquilo opcionalmente sustituido, y heterociclilo opcionalmente sustituido; como un estereoisomero, enantiomero o tautomero del mismo o mezclas de los mismos; o una sal, solvato o prodroga aceptable farmacéuticamente del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10641008P | 2008-10-17 | 2008-10-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR073898A1 true AR073898A1 (es) | 2010-12-09 |
Family
ID=41381681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090104002A AR073898A1 (es) | 2008-10-17 | 2009-10-16 | Compuestos de espiro-oxindol y su uso como agentes terapeuticos. |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8101647B2 (es) |
| EP (1) | EP2350091B1 (es) |
| AR (1) | AR073898A1 (es) |
| CA (1) | CA2741024A1 (es) |
| TW (1) | TWI466889B (es) |
| WO (1) | WO2010045197A1 (es) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY158766A (en) * | 2005-04-11 | 2016-11-15 | Xenon Pharmaceuticals Inc | Spiro-oxindole compounds and their uses as therapeutic agents |
| AR053710A1 (es) * | 2005-04-11 | 2007-05-16 | Xenon Pharmaceuticals Inc | Compuestos espiroheterociclicos y sus usos como agentes terapeuticos |
| US20110294842A9 (en) * | 2006-10-12 | 2011-12-01 | Xenon Pharmaceuticals Inc. | Spiro (furo [3, 2-c] pyridine-3-3' -indol) -2' (1'h)-one derivatives and related compounds for the treatment of sodium-channel mediated diseases, such as pain |
| RU2009117642A (ru) | 2006-10-12 | 2010-11-20 | Ксенон Фармасьютикалз Инк. (Ca) | Применение спирооксиндоловых соединений в качестве терапевтических средств |
| CA2666136A1 (en) * | 2006-10-12 | 2008-04-17 | Xenon Pharmaceuticals Inc. | Tricyclic spiro-oxindole derivatives and their uses as therapeutic agents |
| US8101647B2 (en) | 2008-10-17 | 2012-01-24 | Xenon Pharmaceuticals Inc. | Spiro-oxindole compounds and their use as therapeutic agents |
| HRP20150882T1 (hr) | 2008-10-17 | 2015-09-25 | Xenon Pharmaceuticals Inc. | Spirooksindolski spojevi i njihova upotreba kao terapijska sredstva |
| AR077252A1 (es) | 2009-06-29 | 2011-08-10 | Xenon Pharmaceuticals Inc | Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos |
| WO2011047173A2 (en) * | 2009-10-14 | 2011-04-21 | Xenon Pharmaceuticals Inc. | Pharmaceutical compositions for oral administration |
| NZ599334A (en) | 2009-10-14 | 2014-03-28 | Xenon Pharmaceuticals Inc | Synthetic methods for spiro-oxindole compounds |
| CN102946859B (zh) * | 2010-02-26 | 2016-03-02 | 泽农医药公司 | 用于局部给药的螺-羟吲哚化合物的药物组合物及其作为治疗剂的用途 |
| WO2012049555A1 (en) | 2010-10-13 | 2012-04-19 | Lupin Limited | Spirocyclic compounds as voltage-gated sodium channel modulators |
| CA2853826C (en) | 2011-10-28 | 2021-03-23 | Vanderbilt University | Substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m1 |
| WO2013071201A1 (en) * | 2011-11-11 | 2013-05-16 | Vanderbilt University | Substituted benzylspiroindolin-2-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m1 |
| US9029563B2 (en) | 2012-01-06 | 2015-05-12 | Vanderbilt University | Substituted 1-benzylindolin-2-one analogs as positive allosteric modulators of muscarinic acetylcholine M1 receptors |
| WO2013106795A1 (en) | 2012-01-12 | 2013-07-18 | Vanderbilt University | Substituted 4-(1h~pyrazol-4.yl)benzyl analogues as positive allosteric modulators of machr m1 receptors |
| KR20150002794A (ko) | 2012-04-12 | 2015-01-07 | 제논 파마슈티칼스 인크. | 치료제로서 유용한 스파이로-옥시인돌 화합물을 위한 비대칭적 합성 |
| WO2014106238A1 (en) * | 2012-12-31 | 2014-07-03 | Fang, Qun, Kevin | Heterocyclic compounds and methods of use thereof |
| US9212182B2 (en) | 2013-06-12 | 2015-12-15 | Amgen Inc. | Bicyclic sulfonamide compounds as sodium channel inhibitors |
| WO2015051043A1 (en) | 2013-10-01 | 2015-04-09 | Amgen Inc. | Biaryl acyl-sulfonamide compounds as sodium channel inhibitors |
| EP3126360A1 (en) | 2014-03-29 | 2017-02-08 | Lupin Limited | Sulfonamide compounds as voltage gated sodium channel modulators |
| CN105713001B (zh) * | 2014-12-03 | 2018-05-08 | 华东师范大学 | 3,3’-二氢呋喃螺环氧化吲哚衍生物及其制备方法和应用 |
| AR103636A1 (es) | 2015-02-05 | 2017-05-24 | Teva Pharmaceuticals Int Gmbh | Métodos de tratamiento de neuralgia postherpética con una formulación tópica de un compuesto de espiro-oxindol |
| CR20170392A (es) | 2015-03-02 | 2018-02-20 | Amgen Inc | Compuestos bicíclicos de sulfonamida cetona |
| TW201722938A (zh) | 2015-09-04 | 2017-07-01 | 魯賓有限公司 | 作為電位閘控鈉通道調節子之磺醯胺化合物 |
| CN119119017A (zh) | 2015-12-18 | 2024-12-13 | 美国安进公司 | 烷基二氢喹啉磺酰胺化合物 |
| MA44066A (fr) | 2015-12-18 | 2018-10-24 | Amgen Inc | Composés sulfonamides de dihydroquinoline d'alcynyle |
| CN114409665A (zh) | 2016-06-16 | 2022-04-29 | 泽农医药公司 | 螺-吲哚酮化合物的固态形式 |
| US10100060B2 (en) | 2016-06-16 | 2018-10-16 | Xenon Pharmaceuticals Inc. | Asymmetric synthesis of funapide |
| WO2018163077A1 (en) | 2017-03-08 | 2018-09-13 | Lupin Limited | Indanyl compounds as voltage gated sodium channel modulators |
| EP3592747A1 (en) | 2017-03-10 | 2020-01-15 | Council of Scientific and Industrial Research | Spirooxindole compounds as gsk3 inhibitors and process for preparation thereof |
| CN109761993B (zh) * | 2019-01-31 | 2021-03-23 | 广西师范大学 | 螺苯并呋喃-3,3′-喹啉衍生物及其合成方法和应用 |
| JP7739051B2 (ja) | 2020-06-10 | 2025-09-16 | アムジエン・インコーポレーテツド | シクロブチルジヒドロキノリンスルホンアミド化合物 |
| CA3183948A1 (en) | 2020-06-10 | 2021-12-16 | Amgen Inc. | Heteroalkyl dihydroquinoline sulfonamide compounds |
| JP2021195367A (ja) | 2020-06-10 | 2021-12-27 | アムジエン・インコーポレーテツド | シクロプロピルジヒドロキノリンスルホンアミド化合物 |
| AU2024306684A1 (en) * | 2023-06-28 | 2025-08-07 | Avelos Therapeutics Inc. | Substituted spiro compound derivatives and their pharmaceutical use |
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|---|---|---|---|---|
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-
2009
- 2009-10-13 US US12/577,799 patent/US8101647B2/en not_active Expired - Fee Related
- 2009-10-13 EP EP09741118.5A patent/EP2350091B1/en not_active Not-in-force
- 2009-10-13 WO PCT/US2009/060455 patent/WO2010045197A1/en not_active Ceased
- 2009-10-13 CA CA2741024A patent/CA2741024A1/en not_active Abandoned
- 2009-10-16 AR ARP090104002A patent/AR073898A1/es unknown
- 2009-10-16 TW TW98135185A patent/TWI466889B/zh not_active IP Right Cessation
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|---|---|
| US8101647B2 (en) | 2012-01-24 |
| US20110112162A9 (en) | 2011-05-12 |
| EP2350091A1 (en) | 2011-08-03 |
| US20100099728A1 (en) | 2010-04-22 |
| WO2010045197A1 (en) | 2010-04-22 |
| EP2350091B1 (en) | 2015-06-03 |
| TW201022275A (en) | 2010-06-16 |
| CA2741024A1 (en) | 2010-04-22 |
| TWI466889B (zh) | 2015-01-01 |
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