JP2005527587A5 - - Google Patents
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- JP2005527587A5 JP2005527587A5 JP2003584051A JP2003584051A JP2005527587A5 JP 2005527587 A5 JP2005527587 A5 JP 2005527587A5 JP 2003584051 A JP2003584051 A JP 2003584051A JP 2003584051 A JP2003584051 A JP 2003584051A JP 2005527587 A5 JP2005527587 A5 JP 2005527587A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- groups
- group
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 125000000217 alkyl group Chemical group 0.000 claims 863
- 125000003118 aryl group Chemical group 0.000 claims 802
- 125000000623 heterocyclic group Chemical group 0.000 claims 565
- 125000004103 aminoalkyl group Chemical group 0.000 claims 247
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 106
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 98
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 95
- 125000005128 aryl amino alkyl group Chemical group 0.000 claims 92
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims 83
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 76
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 74
- 125000003277 amino group Chemical group 0.000 claims 68
- 125000003545 alkoxy group Chemical group 0.000 claims 63
- 125000004104 aryloxy group Chemical group 0.000 claims 63
- 229910052739 hydrogen Inorganic materials 0.000 claims 56
- -1 guanidinyl groups Chemical group 0.000 claims 43
- 125000000304 alkynyl group Chemical group 0.000 claims 42
- 150000001875 compounds Chemical class 0.000 claims 39
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 38
- 150000003839 salts Chemical class 0.000 claims 36
- 125000001769 aryl amino group Chemical group 0.000 claims 35
- 125000003342 alkenyl group Chemical group 0.000 claims 34
- 125000003282 alkyl amino group Chemical group 0.000 claims 34
- 125000004663 dialkyl amino group Chemical group 0.000 claims 33
- 125000004986 diarylamino group Chemical group 0.000 claims 30
- 239000002246 antineoplastic agent Substances 0.000 claims 21
- 239000003814 drug Substances 0.000 claims 18
- 229910052760 oxygen Inorganic materials 0.000 claims 16
- 206010028980 Neoplasm Diseases 0.000 claims 12
- 201000011510 cancer Diseases 0.000 claims 12
- 229910052717 sulfur Inorganic materials 0.000 claims 12
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims 9
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 125000005110 aryl thio group Chemical group 0.000 claims 6
- 229940079593 drug Drugs 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- 125000005429 oxyalkyl group Chemical group 0.000 claims 6
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- 241000257303 Hymenoptera Species 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000003107 substituted aryl group Chemical group 0.000 claims 3
- 150000004678 hydrides Chemical class 0.000 claims 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 2
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 2
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 1
- VIDDDLSZDPUIHF-UHFFFAOYSA-N 5-fluoro-3-[6-(4-methylpiperazin-1-yl)-1h-benzimidazol-2-yl]quinolin-4-amine Chemical compound C1CN(C)CCN1C1=CC=C(N=C(N2)C=3C(=C4C(F)=CC=CC4=NC=3)N)C2=C1 VIDDDLSZDPUIHF-UHFFFAOYSA-N 0.000 claims 1
- YASAKCUCGLMORW-UHFFFAOYSA-N Rosiglitazone Natural products C=1C=CC=NC=1N(C)CCOC(C=C1)=CC=C1CC1SC(=O)NC1=O YASAKCUCGLMORW-UHFFFAOYSA-N 0.000 claims 1
- PIQCTGMSNWUMAF-UHFFFAOYSA-N chembl522892 Chemical compound C1CN(C)CCN1C1=CC=C(NC(=N2)C=3C(NC4=CC=CC(F)=C4C=3N)=O)C2=C1 PIQCTGMSNWUMAF-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 229960004586 rosiglitazone Drugs 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/116,117 US20030028018A1 (en) | 2000-09-11 | 2002-04-05 | Quinolinone derivatives |
| PCT/US2003/010463 WO2003087095A1 (en) | 2002-04-05 | 2003-04-04 | Quinolinone derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005527587A JP2005527587A (ja) | 2005-09-15 |
| JP2005527587A5 true JP2005527587A5 (enExample) | 2006-06-22 |
Family
ID=29248193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003584051A Pending JP2005527587A (ja) | 2002-04-05 | 2003-04-04 | キノリノン誘導体 |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US20030028018A1 (enExample) |
| EP (1) | EP1497287B1 (enExample) |
| JP (1) | JP2005527587A (enExample) |
| KR (1) | KR101035894B1 (enExample) |
| CN (1) | CN1659165A (enExample) |
| AP (1) | AP2070A (enExample) |
| AT (1) | ATE489092T1 (enExample) |
| AU (1) | AU2003226275B2 (enExample) |
| BR (1) | BR0308996A (enExample) |
| CA (1) | CA2481055C (enExample) |
| DE (1) | DE60335096D1 (enExample) |
| EA (1) | EA010393B1 (enExample) |
| EC (1) | ECSP045411A (enExample) |
| ES (1) | ES2357289T3 (enExample) |
| HR (1) | HRP20041031B1 (enExample) |
| IL (2) | IL164324A0 (enExample) |
| MA (1) | MA28122A1 (enExample) |
| MX (1) | MXPA04009739A (enExample) |
| NO (1) | NO331021B1 (enExample) |
| NZ (1) | NZ536068A (enExample) |
| PL (1) | PL209412B1 (enExample) |
| PT (1) | PT1497287E (enExample) |
| SG (1) | SG143985A1 (enExample) |
| WO (1) | WO2003087095A1 (enExample) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2334641T3 (es) | 2000-09-01 | 2010-03-15 | Novartis Vaccines And Diagnostics, Inc. | Derivados aza heterociclicos y su uso terapeutico. |
| US20030028018A1 (en) * | 2000-09-11 | 2003-02-06 | Chiron Coporation | Quinolinone derivatives |
| NZ524717A (en) * | 2000-09-11 | 2004-09-24 | Chiron Corp | Quinolinone derivatives |
| JP2004536113A (ja) * | 2001-07-03 | 2004-12-02 | カイロン コーポレイション | チロシンキナーゼおよびセリン／スレオニンキナーゼのインヒビターとしてのインダゾールベンズイミダゾール化合物 |
| US7642278B2 (en) * | 2001-07-03 | 2010-01-05 | Novartis Vaccines And Diagnostics, Inc. | Indazole benzimidazole compounds |
| US7169788B2 (en) | 2001-10-30 | 2007-01-30 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| US7825132B2 (en) * | 2002-08-23 | 2010-11-02 | Novartis Vaccines And Diagnostics, Inc. | Inhibition of FGFR3 and treatment of multiple myeloma |
| CA2496164C (en) * | 2002-08-23 | 2010-11-09 | Chiron Corporation | Benzimidazole quinolinones and uses thereof |
| US20050256157A1 (en) * | 2002-08-23 | 2005-11-17 | Chiron Corporation | Combination therapy with CHK1 inhibitors |
| EP1545529A4 (en) * | 2002-09-30 | 2010-03-03 | Bristol Myers Squibb Co | NEW TYROSINE KINASE HEMMER |
| US7838527B2 (en) * | 2002-11-13 | 2010-11-23 | Novartis Vaccines And Diagnostics, Inc. | Methods of treating cancer and related methods |
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| KR101387985B1 (ko) * | 2005-01-27 | 2014-04-25 | 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 | 전이 종양의 치료 |
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| US7582634B2 (en) * | 2005-02-18 | 2009-09-01 | Wyeth | 7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor |
| US20060189619A1 (en) * | 2005-02-24 | 2006-08-24 | Wyeth | 3-({4-[2-(4-Tert-butylphenyl)-1h-benzimidazol-4-yl]piperazin-1-yl}methyl)pyrido[2,3-b]]pyrazi ne compounds |
| PT1885187E (pt) | 2005-05-13 | 2013-12-16 | Novartis Ag | Métodos para o tratamento de cancro resistente a fármacos |
| PL1888556T3 (pl) * | 2005-05-17 | 2012-03-30 | Novartis Ag | Metody syntetyzowania związków heterocyklicznych |
| US7531542B2 (en) * | 2005-05-18 | 2009-05-12 | Wyeth | Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor |
| RU2425041C2 (ru) | 2005-05-23 | 2011-07-27 | Новартис Аг | Кристаллические и другие формы солей, образованных из молочной кислоты и 4-амино-5-фтор-3-[6-(4-метилпиперазин-1-ил)-1н-бензимидазол-2-ил]-1н-хинолин-2-она |
| US7582636B2 (en) * | 2005-05-26 | 2009-09-01 | Wyeth | Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor |
| AR062545A1 (es) | 2005-11-29 | 2008-11-19 | Novartis Ag | Formulaciones estables de quinolinonas |
| RU2008127252A (ru) | 2005-12-08 | 2010-01-20 | Новартис АГ (CH) | Эффекты ингибиторов fgfr3 на транскрипцию генов |
| CN100488960C (zh) * | 2006-03-09 | 2009-05-20 | 中国药科大学 | 2-位取代的喹诺酮类化合物及其在制药中的应用 |
| US8138205B2 (en) * | 2006-07-07 | 2012-03-20 | Kalypsys, Inc. | Heteroarylalkoxy-substituted quinolone inhibitors of PDE4 |
| JP5280357B2 (ja) * | 2006-07-07 | 2013-09-04 | スティーブン・ピー・ガベック | Ｐｄｅ４の二環式ヘテロアリール阻害剤 |
| US8481553B2 (en) | 2010-04-06 | 2013-07-09 | Brigham Young University | Antimetastatic compounds |
| WO2012027392A2 (en) * | 2010-08-24 | 2012-03-01 | Brigham Young University | Antimetastatic compounds |
| WO2013063003A1 (en) | 2011-10-28 | 2013-05-02 | Novartis Ag | Method of treating gastrointestinal stromal tumors |
| MX2014009303A (es) | 2012-01-31 | 2014-10-14 | Novartis Ag | Combinacion de un inhibidor de rtk con un anti-estrogeno y uso del mismo para el tratamiento de cancer. |
| IN2014DN10801A (enExample) | 2012-07-11 | 2015-09-04 | Novartis Ag | |
| WO2014058785A1 (en) | 2012-10-10 | 2014-04-17 | Novartis Ag | Combination therapy |
| MX363708B (es) | 2013-10-14 | 2019-03-29 | Eisai R&D Man Co Ltd | Compuestos de quinolina selectivamente sustituidos. |
| SG10201704327RA (en) | 2013-10-14 | 2017-06-29 | Eisai R&D Man Co Ltd | Selectively substituted quinoline compounds |
| PT3157566T (pt) | 2014-06-17 | 2019-07-11 | Vertex Pharma | Método para tratamento de cancro utilizando uma combinação de inibidores chk1 e atr |
| EP2977374A1 (en) * | 2014-07-21 | 2016-01-27 | Université de Strasbourg | Molecules presenting dual emission properties |
| RU2768621C1 (ru) | 2015-09-30 | 2022-03-24 | Вертекс Фармасьютикалз Инкорпорейтед | Способ лечения рака с использованием комбинации повреждающих днк средств и ингибиторов atr |
| CN108003150A (zh) * | 2016-10-31 | 2018-05-08 | 河南工业大学 | 4-杂芳基喹啉酮衍生物的制备方法及其应用 |
| MX2020000135A (es) * | 2017-06-27 | 2020-07-22 | Janssen Pharmaceutica Nv | Nuevos compuestos de quinolinona. |
| WO2019101182A1 (en) | 2017-11-24 | 2019-05-31 | Janssen Pharmaceutica Nv | Pyrazolopyridinone compounds |
| JP7329510B2 (ja) | 2017-11-24 | 2023-08-18 | ヤンセン ファーマシューティカ エヌ．ベー． | ピラゾロピリジノン化合物 |
| CN108516973A (zh) * | 2018-03-30 | 2018-09-11 | 广西师范大学 | 3-苯并噻唑-1-(3-二甲氨基)丙基喹啉-4-酮衍生物及其制备方法和应用 |
| CN113227100B (zh) | 2018-12-26 | 2023-05-05 | 詹森药业有限公司 | 噻吩并吡啶酮化合物 |
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2002
- 2002-04-05 US US10/116,117 patent/US20030028018A1/en not_active Abandoned
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2003
- 2003-04-04 CN CN038129094A patent/CN1659165A/zh active Pending
- 2003-04-04 AT AT03746614T patent/ATE489092T1/de active
- 2003-04-04 AP APAP/P/2004/003166A patent/AP2070A/en active
- 2003-04-04 JP JP2003584051A patent/JP2005527587A/ja active Pending
- 2003-04-04 CA CA2481055A patent/CA2481055C/en not_active Expired - Lifetime
- 2003-04-04 ES ES03746614T patent/ES2357289T3/es not_active Expired - Lifetime
- 2003-04-04 NZ NZ536068A patent/NZ536068A/en not_active IP Right Cessation
- 2003-04-04 AU AU2003226275A patent/AU2003226275B2/en not_active Expired
- 2003-04-04 EP EP03746614A patent/EP1497287B1/en not_active Expired - Lifetime
- 2003-04-04 HR HRP20041031AA patent/HRP20041031B1/hr not_active IP Right Cessation
- 2003-04-04 MX MXPA04009739A patent/MXPA04009739A/es active IP Right Grant
- 2003-04-04 EA EA200401318A patent/EA010393B1/ru not_active IP Right Cessation
- 2003-04-04 BR BR0308996-7A patent/BR0308996A/pt not_active Application Discontinuation
- 2003-04-04 WO PCT/US2003/010463 patent/WO2003087095A1/en not_active Ceased
- 2003-04-04 PL PL372871A patent/PL209412B1/pl unknown
- 2003-04-04 DE DE60335096T patent/DE60335096D1/de not_active Expired - Lifetime
- 2003-04-04 KR KR1020047015851A patent/KR101035894B1/ko not_active Expired - Fee Related
- 2003-04-04 IL IL16432403A patent/IL164324A0/xx unknown
- 2003-04-04 PT PT03746614T patent/PT1497287E/pt unknown
- 2003-04-04 SG SG200606999-1A patent/SG143985A1/en unknown
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2004
- 2004-09-28 IL IL164324A patent/IL164324A/en not_active IP Right Cessation
- 2004-10-04 MA MA27887A patent/MA28122A1/fr unknown
- 2004-11-03 NO NO20044776A patent/NO331021B1/no not_active IP Right Cessation
- 2004-11-05 EC EC2004005411A patent/ECSP045411A/es unknown
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2007
- 2007-10-02 US US11/866,296 patent/US20080070906A1/en not_active Abandoned
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2010
- 2010-01-04 US US12/651,612 patent/US20100184754A1/en not_active Abandoned