JP2011507896A5 - - Google Patents
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- Publication number
- JP2011507896A5 JP2011507896A5 JP2010539862A JP2010539862A JP2011507896A5 JP 2011507896 A5 JP2011507896 A5 JP 2011507896A5 JP 2010539862 A JP2010539862 A JP 2010539862A JP 2010539862 A JP2010539862 A JP 2010539862A JP 2011507896 A5 JP2011507896 A5 JP 2011507896A5
- Authority
- JP
- Japan
- Prior art keywords
- compound according
- pyrrolo
- phenylamino
- pyrimidine
- fluoro
- 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 16
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 239000002246 antineoplastic agent Substances 0.000 claims 3
- 229940127089 cytotoxic agent Drugs 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 230000011987 methylation Effects 0.000 claims 3
- 238000007069 methylation reaction Methods 0.000 claims 3
- 241000124008 Mammalia Species 0.000 claims 2
- 230000002159 abnormal effect Effects 0.000 claims 2
- 230000010261 cell growth Effects 0.000 claims 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- 230000003463 hyperproliferative effect Effects 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- -1 (2,2-dimethyl- [1,3] dioxolane-4- Yl) -methyl Chemical group 0.000 claims 1
- FJUFYWCGLPTBES-SNVBAGLBSA-N 5-chloro-n-[(2r)-2,3-dihydroxypropoxy]-7-(2-fluoro-4-iodoanilino)pyrrolo[1,2-c]pyrimidine-6-carboxamide Chemical compound OC[C@@H](O)CONC(=O)C=1C(Cl)=C2C=CN=CN2C=1NC1=CC=C(I)C=C1F FJUFYWCGLPTBES-SNVBAGLBSA-N 0.000 claims 1
- KPWZPMWRPNZLDJ-UHFFFAOYSA-N 7-(2-fluoro-4-iodoanilino)-n-(2-hydroxyethoxy)pyrrolo[1,2-c]pyrimidine-6-carboxamide Chemical compound OCCONC(=O)C=1C=C2C=CN=CN2C=1NC1=CC=C(I)C=C1F KPWZPMWRPNZLDJ-UHFFFAOYSA-N 0.000 claims 1
- BIWQEXNBGHYRKO-UHFFFAOYSA-N 7-(2-fluoro-4-iodoanilino)-n-piperidin-4-yloxypyrrolo[1,2-c]pyrimidine-6-carboxamide Chemical compound FC1=CC(I)=CC=C1NC1=C(C(=O)NOC2CCNCC2)C=C2N1C=NC=C2 BIWQEXNBGHYRKO-UHFFFAOYSA-N 0.000 claims 1
- RAZHOLJAHOLZCC-UHFFFAOYSA-N 7-(2-fluoro-4-methylsulfanylanilino)-n-(2-hydroxyethoxy)pyrrolo[1,2-c]pyrimidine-6-carboxamide Chemical compound FC1=CC(SC)=CC=C1NC1=C(C(=O)NOCCO)C=C2N1C=NC=C2 RAZHOLJAHOLZCC-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000002393 azetidinyl group Chemical group 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- CEPCVVVQVRUEOJ-GFCCVEGCSA-N n-[(2r)-2,3-dihydroxypropoxy]-7-(2-fluoro-4-iodoanilino)pyrrolo[1,2-c]pyrimidine-6-carboxamide Chemical compound OC[C@@H](O)CONC(=O)C=1C=C2C=CN=CN2C=1NC1=CC=C(I)C=C1F CEPCVVVQVRUEOJ-GFCCVEGCSA-N 0.000 claims 1
- LARNVBSFWPDTQZ-GFCCVEGCSA-N n-[(2r)-2,3-dihydroxypropoxy]-7-(2-fluoro-4-methylsulfanylanilino)pyrrolo[1,2-c]pyrimidine-6-carboxamide Chemical compound FC1=CC(SC)=CC=C1NC1=C(C(=O)NOC[C@H](O)CO)C=C2N1C=NC=C2 LARNVBSFWPDTQZ-GFCCVEGCSA-N 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1594207P | 2007-12-21 | 2007-12-21 | |
| US61/015,942 | 2007-12-21 | ||
| PCT/US2008/087626 WO2009082687A1 (en) | 2007-12-21 | 2008-12-19 | Azaindolizines and methods of use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011507896A JP2011507896A (ja) | 2011-03-10 |
| JP2011507896A5 true JP2011507896A5 (enExample) | 2012-01-19 |
| JP5710269B2 JP5710269B2 (ja) | 2015-04-30 |
Family
ID=40352017
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010539862A Expired - Fee Related JP5710269B2 (ja) | 2007-12-21 | 2008-12-19 | アザインドリジン類と使用方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8486963B2 (enExample) |
| EP (1) | EP2220092B1 (enExample) |
| JP (1) | JP5710269B2 (enExample) |
| KR (1) | KR20100099185A (enExample) |
| CN (1) | CN101945875B (enExample) |
| AU (1) | AU2008340247B2 (enExample) |
| BR (1) | BRPI0819505A2 (enExample) |
| CA (1) | CA2708176A1 (enExample) |
| ES (1) | ES2387707T3 (enExample) |
| IL (1) | IL206125A (enExample) |
| NZ (1) | NZ586575A (enExample) |
| WO (1) | WO2009082687A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102020651B (zh) | 2010-11-02 | 2012-07-18 | 北京赛林泰医药技术有限公司 | 6-芳基氨基吡啶酮甲酰胺mek抑制剂 |
| KR20130016041A (ko) * | 2011-08-04 | 2013-02-14 | 재단법인 의약바이오컨버젼스연구단 | 신규한 아닐린 유도체 및 이의 용도 |
| KR20130118612A (ko) * | 2012-04-20 | 2013-10-30 | (주)네오믹스 | 신규한 아미노피리딘 유도체 및 이의 용도 |
| US9532987B2 (en) | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
| EP3153469A4 (en) * | 2014-06-03 | 2017-11-29 | Gaia Institute Of Environmental Technology, Inc. | Amorphous silicon for use in foods, drugs, cosmetics and feed, and production method and production device thereof |
| CN109072311A (zh) | 2016-04-15 | 2018-12-21 | 豪夫迈·罗氏有限公司 | 用于癌症的诊断和治疗方法 |
| ES3030506T3 (en) | 2017-05-19 | 2025-06-30 | Nflection Therapeutics Inc | Pyrrolopyridine-aniline compounds for treatment of dermal disorders |
| EP3624795B1 (en) | 2017-05-19 | 2022-04-20 | NFlection Therapeutics, Inc. | Fused heteroaromatic-aniline compounds for treatment of dermal disorders |
| KR102811888B1 (ko) | 2017-09-08 | 2025-05-27 | 에프. 호프만-라 로슈 아게 | 암의 진단 및 치료 방법 |
| EP3752200A1 (en) | 2018-02-13 | 2020-12-23 | Vib Vzw | Targeting minimal residual disease in cancer with rxr antagonists |
| EP3793559A1 (en) | 2018-05-17 | 2021-03-24 | Bayer Aktiengesellschaft | Substituted dihydropyrazolo pyrazine carboxamide derivatives |
| CA3120337A1 (en) | 2018-11-20 | 2020-05-28 | Nflection Therapeutics, Inc. | Naphthyridinone-aniline compounds for treatment of dermal disorders |
| JP7546297B2 (ja) | 2018-11-20 | 2024-09-06 | エヌフレクション セラピューティクス インコーポレイテッド | 皮膚障害の処置のためのチエニル－アニリン化合物 |
| MA55141A (fr) | 2018-11-20 | 2021-09-29 | Nflection Therapeutics Inc | Composés cyanoaryl-aniline pour le traitement d'affections de la peau |
| WO2021094210A1 (en) | 2019-11-12 | 2021-05-20 | Bayer Aktiengesellschaft | Substituted pyrazine carboxamide derivatives as prostaglandin ep3 receptor antagonists |
| WO2024033381A1 (en) | 2022-08-10 | 2024-02-15 | Vib Vzw | Inhibition of tcf4/itf2 in the treatment of cancer |
| WO2026019990A1 (en) | 2024-07-18 | 2026-01-22 | Genentech, Inc. | Methods of treating cancer with anti-ccr8/anti-cd3 bispecific antibodies |
Family Cites Families (58)
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| SU11248A1 (ru) | 1927-03-29 | 1929-09-30 | В.С. Григорьев | Способ очистки антрацена |
| GB8827305D0 (en) | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| JPH08176070A (ja) | 1994-12-19 | 1996-07-09 | Mitsubishi Chem Corp | ジデプシド誘導体及びｐｉ３キナーゼ阻害剤 |
| JPH08175990A (ja) | 1994-12-19 | 1996-07-09 | Mitsubishi Chem Corp | Ｐｉ３キナーゼ阻害剤とその製造法 |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| DK0821671T3 (da) | 1995-04-20 | 2001-04-23 | Pfizer | Arylsulfonylhydroxamsyrederivater som MMP- og TNF-inhibitorer |
| GB9521987D0 (en) | 1995-10-26 | 1996-01-03 | Ludwig Inst Cancer Res | Phosphoinositide 3-kinase modulators |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| ES2183905T3 (es) | 1995-12-20 | 2003-04-01 | Hoffmann La Roche | Inhibidores de metaloproteasa de matriz. |
| JP4471404B2 (ja) | 1996-02-13 | 2010-06-02 | アストラゼネカ ユーケイ リミテッド | Ｖｅｇｆインヒビターとしてのキナゾリン誘導体 |
| ATE211134T1 (de) | 1996-03-05 | 2002-01-15 | 4-anilinochinazolin derivate | |
| EP0818442A3 (en) | 1996-07-12 | 1998-12-30 | Pfizer Inc. | Cyclic sulphone derivatives as inhibitors of metalloproteinases and of the production of tumour necrosis factor |
| HUP9903014A3 (en) | 1996-07-18 | 2000-08-28 | Pfizer | Phosphinate derivatives having matrix metalloprotease inhibitor effect and medicaments containing the same |
| US6153609A (en) | 1996-08-23 | 2000-11-28 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| AU5131998A (en) | 1997-01-06 | 1998-08-03 | Pfizer Inc. | Cyclic sulfone derivatives |
| ES2202796T3 (es) | 1997-02-03 | 2004-04-01 | Pfizer Products Inc. | Derivados de acidos arilsulfonilaminohidroxamicos. |
| JP2000507975A (ja) | 1997-02-07 | 2000-06-27 | ファイザー・インク | Ｎ−ヒドロキシ−β−スルホニルプロピオンアミド誘導体類及びそれらのマトリックスメタロプロテイナーゼ阻害薬としての使用 |
| WO1998035985A1 (en) | 1997-02-12 | 1998-08-20 | The Regents Of The University Of Michigan | Protein markers for lung cancer and use thereof |
| ID23668A (id) | 1997-08-08 | 2000-05-11 | Pfizer Prod Inc | Turunan asam ariloksiarilsulfonilamino hidroksamat |
| GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
| GB9801690D0 (en) | 1998-01-27 | 1998-03-25 | Pfizer Ltd | Therapeutic agents |
| JP4462654B2 (ja) | 1998-03-26 | 2010-05-12 | ソニー株式会社 | 映像素材選択装置及び映像素材選択方法 |
| PA8469501A1 (es) | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico |
| PA8469401A1 (es) | 1998-04-10 | 2000-05-24 | Pfizer Prod Inc | Derivados biciclicos del acido hidroxamico |
| ES2213985T3 (es) | 1998-11-05 | 2004-09-01 | Pfizer Products Inc. | Derivados de hidroxiamida de acido 5-oxo-pirrolidin-2-carboxilico. |
| DK1553097T3 (da) | 1999-02-10 | 2010-12-13 | Astrazeneca Ab | Quinazolinderivat som angiogeneseinhibitor og mellemprodukter dertil |
| CA2377092A1 (en) | 1999-07-16 | 2001-01-25 | Warner-Lambert Company | Method for treating chronic pain using mek inhibitors |
| PL203782B1 (pl) | 1999-11-05 | 2009-11-30 | Astrazeneca Ab | Pochodne chinazoliny,sposoby ich wytwarzania,ich kompozycje farmaceutyczne oraz ich zastosowania |
| DE122008000002I1 (de) | 2000-02-15 | 2008-04-17 | Sugen Inc | Pyrrol substituierte indolin-2-on protein kinase inhibitoren |
| JP2001247477A (ja) | 2000-03-03 | 2001-09-11 | Teikoku Hormone Mfg Co Ltd | 抗腫瘍剤 |
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-
2008
- 2008-12-19 NZ NZ586575A patent/NZ586575A/en not_active IP Right Cessation
- 2008-12-19 EP EP08864072A patent/EP2220092B1/en active Active
- 2008-12-19 CN CN2008801273742A patent/CN101945875B/zh not_active Expired - Fee Related
- 2008-12-19 KR KR1020107013464A patent/KR20100099185A/ko not_active Abandoned
- 2008-12-19 CA CA2708176A patent/CA2708176A1/en not_active Abandoned
- 2008-12-19 JP JP2010539862A patent/JP5710269B2/ja not_active Expired - Fee Related
- 2008-12-19 BR BRPI0819505A patent/BRPI0819505A2/pt not_active IP Right Cessation
- 2008-12-19 US US12/809,047 patent/US8486963B2/en not_active Expired - Fee Related
- 2008-12-19 WO PCT/US2008/087626 patent/WO2009082687A1/en not_active Ceased
- 2008-12-19 ES ES08864072T patent/ES2387707T3/es active Active
- 2008-12-19 AU AU2008340247A patent/AU2008340247B2/en not_active Ceased
-
2010
- 2010-06-01 IL IL206125A patent/IL206125A/en not_active IP Right Cessation