AR045471A1 - Derivados de naftiridina sustituidos como inhibidores del factor inhibidor de la migracion de macrofagos y su uso en el tratamiento de enfermedades en el hombre - Google Patents
Derivados de naftiridina sustituidos como inhibidores del factor inhibidor de la migracion de macrofagos y su uso en el tratamiento de enfermedades en el hombreInfo
- Publication number
- AR045471A1 AR045471A1 ARP040102991A ARP040102991A AR045471A1 AR 045471 A1 AR045471 A1 AR 045471A1 AR P040102991 A ARP040102991 A AR P040102991A AR P040102991 A ARP040102991 A AR P040102991A AR 045471 A1 AR045471 A1 AR 045471A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- group
- nr4r5
- heterocycle
- aryl
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A61P11/06—Antiasthmatics
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
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- A61P37/02—Immunomodulators
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
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- Child & Adolescent Psychology (AREA)
- Transplantation (AREA)
- Psychiatry (AREA)
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- Dermatology (AREA)
Abstract
Se proveen inhibidores del factor inhibidor de la migración de macrófagos (MIF) con una estructura principal de naftiridina que son de utilidad en el tratamiento de una variedad de trastornos, incluyendo el tratamiento de afecciones patológicas asociadas con la actividad del MIF. Los inhibidores del MIF tienen las estructuras de las fórmulas (1), que incluyen estereoisómeros, prodrogas y sales aceptables para uso farmacéutico de los mismos. También se proveen composiciones que contienen un inhibidor de MIF en combinación con un vehículo aceptable para uso farmacéutico, así como métodos para utilizarlos. Reivindicación 1: Un compuesto donde, R se selecciona entre el grupo que consiste en hidrógeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, cicloalquilo, cicloalquilo sustituido, arilo, arilo sustituido, arilalquilo, arilalquilo sustituido, acilalquilo, acilalquilo sustituido, heterociclo, heterociclo sustituido, -(CH2)mC(=O)Ar, y -(CH2)mNR4R5; R1 se selecciona entre el grupo que consiste en -CN, -NO, -NO2, -C(=O)R3, -C(=O)OH, -NHC(=O)R3, -C(=O)OR3, -C(=O)NR4R5, -NR3C(=O)R3, -SO2NR4R5, -NR3SO2R3, -NHSO2R3, -S(O)mR3, -(CH2)mNR4R5, y -(CH2)mC(=O)Ar; R2 se selecciona entre el grupo que consiste en - CH2R3, -NR4R5, -OR3, y -R3; R3 se selecciona independientemente entre el grupo que consiste en alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, cicloalquilo, cicloalquilo sustituido, arilo, arilo sustituido, arilalquilo, arilalquilo sustituido, acilalquilo, acilalquilo sustituido, heterociclo, heterociclo sustituido; R4 y R5 se seleccionan independientemente entre el grupo que consiste en hidrógeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, cicloalquilo, cicloalquilo sustituido, arilo, arilo sustituido, arilalquilo, arilalquilo sustituido, acilalquilo, acilalquilo sustituido, heterociclo, y heterociclo sustituido, o R4 y R5 tomados juntos comprenden heterociclo o heterociclo sustituido; X se selecciona entre el grupo que consiste en hidrógeno, halógeno, -F, -Cl, -CN, -NO, -NO2, -OCF3, -CF3, -NHSO2R3, -C(=O)R3, -C(=O)OR3, -C(=O)NR4R5, -NR3C(=O)R3, -NR3SO2R3, -S(O)mR3, -R3, -OR3, -SR3, -C(=O)OH, -NHC(=O)R3, y -NR4R5; Y se selecciona entre el grupo que consiste en hidrógeno, halógeno, -F, -Cl, -CN, -NO, -NO2, -OCF3, -CF3, -NHSO2R3, -C(=O)R3, -C(=O)OR3, -C(=O)NR4R5, -NR3C(=O)R3, -NR3SO2R3, -S(O)mR3, -R3, -OR3, -SR3, -C(=O)OH, -NHC(=O)R3, y -NR4R5; Z se selecciona entre el grupo que consiste en hidrógeno, halógeno, -F, -Cl, -CN, -NO, -NO2, -OCF3, -CF3, -NHSO2R3, -C(=O)R3, -C(=O)OR3, -C(=O)NR4R5, -NR3C(=O)R3, -NR3SO2R3, -S(O)mR3, -R3, -OR3, -SR3, -C(=O)OH, -NHC(=O)R3, y -NR4R5; Ar se selecciona entre el grupo que consiste en arilo y arilo sustituido; m es independientemente 0, 1, 2, 3 ó 4; y n es 0, 1 ó 2.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49744303P | 2003-08-22 | 2003-08-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR045471A1 true AR045471A1 (es) | 2005-10-26 |
Family
ID=34272569
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP040102991A AR045471A1 (es) | 2003-08-22 | 2004-08-20 | Derivados de naftiridina sustituidos como inhibidores del factor inhibidor de la migracion de macrofagos y su uso en el tratamiento de enfermedades en el hombre |
Country Status (13)
Country | Link |
---|---|
US (2) | US20050124604A1 (es) |
EP (1) | EP1656376A1 (es) |
JP (1) | JP2007503388A (es) |
CN (1) | CN1839133A (es) |
AR (1) | AR045471A1 (es) |
AU (1) | AU2004268941A1 (es) |
BR (1) | BRPI0413695A (es) |
CA (1) | CA2531506A1 (es) |
MX (1) | MXJL06000006A (es) |
PE (1) | PE20051112A1 (es) |
TW (1) | TW200524928A (es) |
UY (1) | UY28483A1 (es) |
WO (1) | WO2005021546A1 (es) |
Families Citing this family (41)
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TW200418829A (en) * | 2003-02-14 | 2004-10-01 | Avanir Pharmaceutics | Inhibitors of macrophage migration inhibitory factor and methods for identifying the same |
AU2006227297A1 (en) * | 2005-03-24 | 2006-09-28 | Avanir Pharmaceuticals | Thienopyridinone derivatives as macrophage migration inhibitory factor inhibitors |
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AU2008241577B2 (en) | 2007-04-18 | 2011-04-07 | Amgen Inc. | Indanone derivatives that inhibit prolyl hydroxylase |
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EP2155746A2 (en) | 2007-05-04 | 2010-02-24 | Amgen, Inc | Diazaquinolones that inhibit prolyl hydroxylase activity |
US9643922B2 (en) | 2008-08-18 | 2017-05-09 | Yale University | MIF modulators |
US9540322B2 (en) | 2008-08-18 | 2017-01-10 | Yale University | MIF modulators |
TW201120037A (en) * | 2009-10-26 | 2011-06-16 | Sunesis Pharmaceuticals Inc | Compounds and methods for treatment of cancer |
US9050334B2 (en) | 2010-07-16 | 2015-06-09 | Innov88 Llc | MIF inhibitors and their uses |
GB2497476B (en) * | 2010-09-06 | 2018-01-10 | Guangzhou Inst Biomed & Health | Amide Compounds |
US9133164B2 (en) * | 2011-04-13 | 2015-09-15 | Innov88 Llc | MIF inhibitors and their uses |
CN103360388B (zh) * | 2012-04-10 | 2017-11-14 | 江苏先声药业有限公司 | 5‑氨基‑1,4‑二氢‑1,8‑萘啶衍生物及其药物组合物和用途 |
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HUE056777T2 (hu) | 2016-12-22 | 2022-03-28 | Amgen Inc | Benzizotiazol-, izotiazolo[3,4-b]piridin-, kinazolin-, ftálazin-, pirido[2,3-d]piridazin- és pirido[2,3-d]pirimidin-származékok mint KRAS G12C inhibitorok tüdõ-, hasnyálmirigy- vagy vastagbélrák kezelésére |
JOP20190272A1 (ar) | 2017-05-22 | 2019-11-21 | Amgen Inc | مثبطات kras g12c وطرق لاستخدامها |
MA50077A (fr) | 2017-09-08 | 2020-07-15 | Amgen Inc | Inhibiteurs de kras g12c et leurs procédés d'utilisation |
CN107556309B (zh) * | 2017-09-11 | 2020-12-01 | 浙江永宁药业股份有限公司 | 多取代四氢萘啶类化合物的药物用途及其制备方法 |
CA3098574A1 (en) | 2018-05-04 | 2019-11-07 | Amgen Inc. | Kras g12c inhibitors and methods of using the same |
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MA52564A (fr) | 2018-05-10 | 2021-03-17 | Amgen Inc | Inhibiteurs de kras g12c pour le traitement du cancer |
MA52765A (fr) | 2018-06-01 | 2021-04-14 | Amgen Inc | Inhibiteurs de kras g12c et leurs procédés d'utilisation |
AU2019284472B2 (en) * | 2018-06-11 | 2024-05-30 | Amgen Inc. | KRAS G12C inhibitors for treating cancer |
CA3100390A1 (en) | 2018-06-12 | 2020-03-12 | Amgen Inc. | Kras g12c inhibitors encompassing piperazine ring and use thereof in the treatment of cancer |
PT3814347T (pt) * | 2018-06-27 | 2023-07-18 | Bristol Myers Squibb Co | Compostos de naftiridinona úteis como ativadores de células t |
HUE064531T2 (hu) | 2018-06-27 | 2024-04-28 | Bristol Myers Squibb Co | Szubsztituált naftiridinon vegyületek mint T-sejt aktivátorok |
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CN111471059B (zh) * | 2019-01-23 | 2022-12-02 | 药捷安康(南京)科技股份有限公司 | Pde9抑制剂及其用途 |
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-
2004
- 2004-08-09 AU AU2004268941A patent/AU2004268941A1/en not_active Abandoned
- 2004-08-09 WO PCT/US2004/025683 patent/WO2005021546A1/en active Application Filing
- 2004-08-09 CA CA002531506A patent/CA2531506A1/en not_active Abandoned
- 2004-08-09 EP EP04780510A patent/EP1656376A1/en not_active Ceased
- 2004-08-09 MX MXJL06000006A patent/MXJL06000006A/es unknown
- 2004-08-09 BR BRPI0413695-0A patent/BRPI0413695A/pt not_active IP Right Cessation
- 2004-08-09 CN CNA2004800241375A patent/CN1839133A/zh active Pending
- 2004-08-09 JP JP2006523903A patent/JP2007503388A/ja active Pending
- 2004-08-17 US US10/920,031 patent/US20050124604A1/en not_active Abandoned
- 2004-08-18 TW TW093124762A patent/TW200524928A/zh unknown
- 2004-08-20 AR ARP040102991A patent/AR045471A1/es not_active Application Discontinuation
- 2004-08-20 UY UY28483A patent/UY28483A1/es not_active Application Discontinuation
- 2004-08-21 PE PE2004000808A patent/PE20051112A1/es not_active Application Discontinuation
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2007
- 2007-03-16 US US11/687,601 patent/US7361760B2/en not_active Expired - Fee Related
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WO2005021546A1 (en) | 2005-03-10 |
CA2531506A1 (en) | 2005-03-10 |
EP1656376A1 (en) | 2006-05-17 |
CN1839133A (zh) | 2006-09-27 |
US20070191388A1 (en) | 2007-08-16 |
US7361760B2 (en) | 2008-04-22 |
AU2004268941A1 (en) | 2005-03-10 |
US20050124604A1 (en) | 2005-06-09 |
JP2007503388A (ja) | 2007-02-22 |
PE20051112A1 (es) | 2006-02-03 |
UY28483A1 (es) | 2005-03-31 |
TW200524928A (en) | 2005-08-01 |
BRPI0413695A (pt) | 2006-10-24 |
MXJL06000006A (es) | 2006-05-04 |
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