JP2006508107A5 - - Google Patents
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- Publication number
- JP2006508107A5 JP2006508107A5 JP2004550489A JP2004550489A JP2006508107A5 JP 2006508107 A5 JP2006508107 A5 JP 2006508107A5 JP 2004550489 A JP2004550489 A JP 2004550489A JP 2004550489 A JP2004550489 A JP 2004550489A JP 2006508107 A5 JP2006508107 A5 JP 2006508107A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- group
- composition
- optionally substituted
- 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
- 0 **=*C(c1c(*)*n*(N*)*1)=*[*+] Chemical compound **=*C(c1c(*)*n*(N*)*1)=*[*+] 0.000 description 10
- QEITZRMTXOMJER-UHFFFAOYSA-N C1C2C(CC3)C3CCC12 Chemical compound C1C2C(CC3)C3CCC12 QEITZRMTXOMJER-UHFFFAOYSA-N 0.000 description 1
- LXNRLNDZSUGVIZ-UHFFFAOYSA-N CC1C(C)(CC2)C2CC1 Chemical compound CC1C(C)(CC2)C2CC1 LXNRLNDZSUGVIZ-UHFFFAOYSA-N 0.000 description 1
- XGOJEEATRXFBJN-UHFFFAOYSA-N CCC(C1)=CC=C(C(C=C2N)C=C=C2OC)N=C1Nc1cccc(OC2C=CC=CC2)c1 Chemical compound CCC(C1)=CC=C(C(C=C2N)C=C=C2OC)N=C1Nc1cccc(OC2C=CC=CC2)c1 XGOJEEATRXFBJN-UHFFFAOYSA-N 0.000 description 1
- FLLVWQWXWWJBLW-UHFFFAOYSA-N CCC(C1)=CC=C(c(cc2N)ccc2OC)N=C1Nc(cc1)ccc1S(=C)=O Chemical compound CCC(C1)=CC=C(c(cc2N)ccc2OC)N=C1Nc(cc1)ccc1S(=C)=O FLLVWQWXWWJBLW-UHFFFAOYSA-N 0.000 description 1
- CXUIMSIUZAGXBG-UHFFFAOYSA-O CCC(C1)=CCC(C(CC2N)=CC=C2OC)N=C1[NH2+]c1cc(C)cc(C)c1 Chemical compound CCC(C1)=CCC(C(CC2N)=CC=C2OC)N=C1[NH2+]c1cc(C)cc(C)c1 CXUIMSIUZAGXBG-UHFFFAOYSA-O 0.000 description 1
- CBEGTFNCNBGGFY-UHFFFAOYSA-O CCC(C1)=CCC(c(cc2N)ccc2OC)N=C1[NH2+]c1cccc(-c2ccccc2)c1 Chemical compound CCC(C1)=CCC(c(cc2N)ccc2OC)N=C1[NH2+]c1cccc(-c2ccccc2)c1 CBEGTFNCNBGGFY-UHFFFAOYSA-O 0.000 description 1
- SJYXRQQGBIFRBO-UHFFFAOYSA-O CCC(CC(C)[NH2+]C(C1)C=CC=C1C(OCC)=O)=CC=C(C(C=C1N)=CCC1OC)N Chemical compound CCC(CC(C)[NH2+]C(C1)C=CC=C1C(OCC)=O)=CC=C(C(C=C1N)=CCC1OC)N SJYXRQQGBIFRBO-UHFFFAOYSA-O 0.000 description 1
- QJTBHYFTQAEADC-UHFFFAOYSA-O COC(C(N)=C1)=CCC1C(N)=CC1C(CC([NH2+]c2ccccc2)=C)C1 Chemical compound COC(C(N)=C1)=CCC1C(N)=CC1C(CC([NH2+]c2ccccc2)=C)C1 QJTBHYFTQAEADC-UHFFFAOYSA-O 0.000 description 1
- WAGDBAZSJRNKMB-UHFFFAOYSA-O COc(c(N)c1)ccc1-c1cccc([NH2+]C(C2)C=CC=C2F)n1 Chemical compound COc(c(N)c1)ccc1-c1cccc([NH2+]C(C2)C=CC=C2F)n1 WAGDBAZSJRNKMB-UHFFFAOYSA-O 0.000 description 1
- WSXBWBYDNIVHHN-UHFFFAOYSA-O COc1cc([NH2+]c2nc(-c(cc3N)ccc3OC)ccn2)ccc1 Chemical compound COc1cc([NH2+]c2nc(-c(cc3N)ccc3OC)ccn2)ccc1 WSXBWBYDNIVHHN-UHFFFAOYSA-O 0.000 description 1
- VORBWXREWDZPFB-MKMHIBQSSA-N C[C@H](CC1)C2(C)C1C1C2CC1 Chemical compound C[C@H](CC1)C2(C)C1C1C2CC1 VORBWXREWDZPFB-MKMHIBQSSA-N 0.000 description 1
- IQZDIBKPVOENRY-UHFFFAOYSA-N C[OH+][NH+](c(cc(cc1)-c2ccnc(NC3(C4)C=CC=C4C3)n2)c1O)[O-] Chemical compound C[OH+][NH+](c(cc(cc1)-c2ccnc(NC3(C4)C=CC=C4C3)n2)c1O)[O-] IQZDIBKPVOENRY-UHFFFAOYSA-N 0.000 description 1
- NDJURPXFXIUTPX-UHFFFAOYSA-N Cc1cc(Nc2nc(-c(cc3N)ccc3OC)ccn2)ccc1 Chemical compound Cc1cc(Nc2nc(-c(cc3N)ccc3OC)ccn2)ccc1 NDJURPXFXIUTPX-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42404302P | 2002-11-05 | 2002-11-05 | |
| PCT/US2003/035188 WO2004041810A1 (en) | 2002-11-05 | 2003-11-05 | Compounds useful as inhibitors of jak and other protein kinases |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010139840A Division JP2010195838A (ja) | 2002-11-05 | 2010-06-18 | Jakおよび他のプロテインキナーゼのインヒビターとして有用な化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006508107A JP2006508107A (ja) | 2006-03-09 |
| JP2006508107A5 true JP2006508107A5 (https=) | 2006-08-31 |
Family
ID=32312743
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004550489A Pending JP2006508107A (ja) | 2002-11-05 | 2003-11-05 | Jakおよび他のプロテインキナーゼのインヒビターとして有用な化合物 |
| JP2010139840A Pending JP2010195838A (ja) | 2002-11-05 | 2010-06-18 | Jakおよび他のプロテインキナーゼのインヒビターとして有用な化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010139840A Pending JP2010195838A (ja) | 2002-11-05 | 2010-06-18 | Jakおよび他のプロテインキナーゼのインヒビターとして有用な化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7348335B2 (https=) |
| EP (1) | EP1560824A1 (https=) |
| JP (2) | JP2006508107A (https=) |
| AU (2) | AU2003286895A1 (https=) |
| CA (1) | CA2507406A1 (https=) |
| WO (1) | WO2004041810A1 (https=) |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| HRP20050089B1 (hr) | 2002-07-29 | 2015-06-19 | Rigel Pharmaceuticals | Upotreba 2,4 pirimidindiaminskog spoja za proizvodnju lijeka za lijeäśenje ili sprjeäśavanje autoimunosne bolesti |
| AU2003262642B2 (en) * | 2002-08-14 | 2010-06-17 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors and uses thereof |
| AU2003286876A1 (en) * | 2002-11-01 | 2004-06-07 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of jak and other protein kinases |
| US20050014753A1 (en) * | 2003-04-04 | 2005-01-20 | Irm Llc | Novel compounds and compositions as protein kinase inhibitors |
| EP1648875A1 (en) | 2003-07-30 | 2006-04-26 | Cyclacel Limited | 2-aminophenyl-4-phenylpyrimidines as kinase inhibitors |
| WO2005012294A1 (en) | 2003-07-30 | 2005-02-10 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases |
| CA2545422C (en) * | 2003-12-03 | 2015-06-02 | Cytopia Research Pty Ltd | Tubulin inhibitors |
| CA2579007A1 (en) * | 2004-09-10 | 2006-03-16 | Altana Pharma Ag | Ciclesonide and syk inhibitor combination and methods of use thereof |
| JP2008515986A (ja) * | 2004-10-13 | 2008-05-15 | ワイス | N−ベンゼンスルホニル置換アニリノ−ピリミジン類似物 |
| AU2006206458B2 (en) | 2005-01-19 | 2012-10-25 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
| BRPI0607062A2 (pt) | 2005-02-28 | 2009-08-04 | Japan Tobacco Inc | composto de aminopiridina com atividade inibidora de syk, composição farmacêutica e agente terapêutico compreendendo os mesmos |
| BRPI0610876B8 (pt) | 2005-06-08 | 2021-05-25 | Rigel Pharmaceuticals Inc | composto, formulação farmacêutica, e métodos de inibir uma atividade de uma jak cinase, e de inibir uma cascata de transdução de sinal em que jak3 cinase desempenha um papel |
| US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| KR20080110998A (ko) * | 2006-01-30 | 2008-12-22 | 엑셀리시스, 인코포레이티드 | Jak2 조절자로서 4아릴2아미노피리미딘 또는 4아릴2아미노알킬피리미딘 및 이들을 포함하는 약제학적 조성물 |
| ES2622493T3 (es) | 2006-02-24 | 2017-07-06 | Rigel Pharmaceuticals, Inc. | Composiciones y métodos para la inhibición de la ruta de JAK |
| EP2418202B1 (en) | 2006-03-31 | 2014-01-29 | Novartis AG | (4-[4-[5-(substituted amino)-pyridin-2-yl]phenyl]-cyclohexyl)-acetic acid derivatives as DGAT inhibitors |
| WO2007120593A1 (en) * | 2006-04-12 | 2007-10-25 | Wyeth | Anilino-pyrimidine phenyl and benzothiophene analogs |
| WO2008009458A1 (en) * | 2006-07-21 | 2008-01-24 | Novartis Ag | 2, 4 -di (arylaminio) -pyrimidine-5-carboxamide compounds as jak kinases inhibitors |
| JP5161233B2 (ja) | 2006-10-19 | 2013-03-13 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 自己免疫疾患の処置のためのjakキナーゼの阻害剤としての2,4−ピリミジンアミン誘導体 |
| US20080153822A1 (en) * | 2006-11-30 | 2008-06-26 | Martin Augustin | Methods of treating pain |
| WO2008073865A2 (en) * | 2006-12-11 | 2008-06-19 | Novartis Ag | Method of preventing or treating myocardial ischemia |
| AU2013201306B2 (en) * | 2007-03-12 | 2015-11-12 | Glaxosmithkline Llc | Phenyl Amino Pyrimidine Compounds and Uses Thereof |
| AU2016200866B2 (en) * | 2007-03-12 | 2017-06-22 | Glaxosmithkline Llc | Phenyl amino pyrimidine compounds and uses thereof |
| KR101566840B1 (ko) * | 2007-03-12 | 2015-11-06 | 와이엠 바이오사이언시즈 오스트레일리아 피티와이 엘티디 | 페닐 아미노 피리미딘 화합물 및 이의 용도 |
| JP5611826B2 (ja) * | 2007-09-04 | 2014-10-22 | ザ スクリプス リサーチ インスティテュート | タンパク質キナーゼ阻害剤としての置換されたピリミジニル−アミン |
| HUE030912T2 (en) | 2008-02-15 | 2017-06-28 | Rigel Pharmaceuticals Inc | Pyrimidine-2-amine compounds and their use as inhibitors of yak kinases |
| WO2009107391A1 (ja) * | 2008-02-27 | 2009-09-03 | 武田薬品工業株式会社 | 6員芳香環含有化合物 |
| GB0805477D0 (en) * | 2008-03-26 | 2008-04-30 | Univ Nottingham | Pyrimidines triazines and their use as pharmaceutical agents |
| US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| US8063058B2 (en) | 2008-04-16 | 2011-11-22 | Portola Pharmaceuticals, Inc. | Inhibitors of syk and JAK protein kinases |
| AU2009238590A1 (en) | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| JP2011523551A (ja) * | 2008-05-15 | 2011-08-18 | ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル | 血管形成の調節の新規ターゲット |
| EP2488503A1 (en) * | 2009-10-12 | 2012-08-22 | Myrexis, Inc. | Amino - pyrimidine compounds as inhibitors of tbkl and/or ikk epsilon |
| EP2512246B1 (en) * | 2009-12-17 | 2015-09-30 | Merck Sharp & Dohme Corp. | Aminopyrimidines as syk inhibitors |
| NZ601267A (en) | 2009-12-23 | 2014-03-28 | Takeda Pharmaceutical | Fused heteroaromatic pyrrolidinones as syk inhibitors |
| EP2975027A1 (en) | 2010-11-01 | 2016-01-20 | Portola Pharmaceuticals, Inc. | Nicotinamides as jak kinase modulators |
| WO2012066065A1 (en) * | 2010-11-17 | 2012-05-24 | Novartis Ag | Phenyl-heteroaryl amine compounds and their uses |
| CN103298787A (zh) * | 2010-11-17 | 2013-09-11 | 诺瓦提斯公司 | 3-(氨基芳基)-吡啶化合物 |
| JP5959537B2 (ja) * | 2011-01-28 | 2016-08-02 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 置換ピリジニル−ピリミジン及び医薬としてのその使用 |
| US9145391B2 (en) | 2011-05-10 | 2015-09-29 | Merck Sharp & Dohme Corp. | Bipyridylaminopyridines as Syk inhibitors |
| EP2723739B1 (en) | 2011-06-22 | 2016-08-24 | Takeda Pharmaceutical Company Limited | Substituted 6-aza-isoindolin-1-one derivatives |
| MX363551B (es) | 2011-11-23 | 2019-03-27 | Portola Pharmaceuticals Inc Star | Compuestos derivados de pirazina como inhibidores de cinasa. |
| WO2013110585A1 (en) | 2012-01-23 | 2013-08-01 | Boehringer Ingelheim International Gmbh | 5, 8 -dihydro- 6h- pyrazolo [3, 4 -h] quinazolines as igf-lr/lr inhibitors |
| WO2013175415A1 (en) * | 2012-05-23 | 2013-11-28 | Piramal Enterprises Limited | Substituted pyrimidine compounds and uses thereof |
| US8809359B2 (en) | 2012-06-29 | 2014-08-19 | Ym Biosciences Australia Pty Ltd | Phenyl amino pyrimidine bicyclic compounds and uses thereof |
| WO2014013014A1 (en) | 2012-07-18 | 2014-01-23 | Fundació Privada Centre De Regulació Genòmica (Crg) | Jak inhibitors for activation of epidermal stem cell populations |
| US9353066B2 (en) | 2012-08-20 | 2016-05-31 | Merck Sharp & Dohme Corp. | Substituted phenyl-Spleen Tyrosine Kinase (Syk) inhibitors |
| WO2014058921A2 (en) | 2012-10-08 | 2014-04-17 | Portola Pharmaceuticals, Inc. | Substituted pyrimidinyl kinase inhibitors |
| SI3126351T1 (sl) | 2014-04-02 | 2018-11-30 | Bristol-Myers Squibb Company | Biaril kinazni inhibitorji |
| TWI729644B (zh) | 2014-06-12 | 2021-06-01 | 美商西爾拉癌症醫學公司 | N-(氰基甲基)-4-(2-(4-𠰌啉基苯基胺基)嘧啶-4-基)苯甲醯胺 |
| EP3356330B1 (en) | 2015-10-01 | 2019-11-20 | Bristol-Myers Squibb Company | Biaryl kinase inhibitors |
| KR102704295B1 (ko) | 2015-10-01 | 2024-09-05 | 브리스톨-마이어스 스큅 컴퍼니 | 비아릴 키나제 억제제 |
| WO2018041989A1 (en) | 2016-09-02 | 2018-03-08 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for diagnosing and treating refractory celiac disease type 2 |
| EA202192575A1 (ru) | 2019-03-21 | 2022-01-14 | Онксео | Соединения dbait в сочетании с ингибиторами киназ для лечения рака |
| EP3947737A2 (en) | 2019-04-02 | 2022-02-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods of predicting and preventing cancer in patients having premalignant lesions |
| EP3955920A1 (en) | 2019-04-16 | 2022-02-23 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Use of jak inhibitors for the treatment of painful conditions involving nav1.7 channels |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| CN113549018B (zh) * | 2020-04-24 | 2024-02-27 | 中国药科大学 | 蛋白激酶抑制剂及其衍生物,制备方法、药物组合物和应用 |
| CN115403516B (zh) * | 2021-08-03 | 2024-01-26 | 河南省儿童医院郑州儿童医院 | 含3,4,5-三取代基苯环的芳杂环化合物、药物组合物及其制备方法和应用 |
| CN115703760B (zh) * | 2021-08-11 | 2024-05-31 | 山东大学 | 2,4-二取代嘧啶类细胞周期蛋白依赖性激酶酶抑制剂及其制备方法和应用 |
| TW202333718A (zh) * | 2022-02-03 | 2023-09-01 | 美商奈可薩斯醫藥有限公司 | 芳基烴受體促效劑及其用途 |
| WO2023222565A1 (en) | 2022-05-16 | 2023-11-23 | Institut National de la Santé et de la Recherche Médicale | Methods for assessing the exhaustion of hematopoietic stems cells induced by chronic inflammation |
| WO2024051702A1 (zh) * | 2022-09-05 | 2024-03-14 | 浙江同源康医药股份有限公司 | 用作cdk4激酶抑制剂的化合物及其应用 |
| CN117886801B (zh) * | 2024-03-14 | 2024-05-17 | 中国药科大学 | 吡啶酮嘧啶类cdk抑制剂及其制备方法和应用 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4218458A (en) * | 1978-06-23 | 1980-08-19 | Janssen Pharmaceutica, N.V. | Heterocyclic derivatives of (4-aryloxy-methyl-1,3-dioxolan-2-yl)methyl-1H-imidazoles and 1H-1,2,4-triazoles |
| GB8412184D0 (en) * | 1984-05-12 | 1984-06-20 | Fisons Plc | Biologically active nitrogen heterocycles |
| WO1995009851A1 (en) | 1993-10-01 | 1995-04-13 | Ciba-Geigy Ag | Pharmacologically active pyrimidineamine derivatives and processes for the preparation thereof |
| PT672041E (pt) | 1993-10-01 | 2002-04-29 | Novartis Ag | Derivados da piridina farmacologicamente activos e processos para a sua preparacao |
| WO1995009847A1 (en) | 1993-10-01 | 1995-04-13 | Ciba-Geigy Ag | Pyrimidineamine derivatives and processes for the preparation thereof |
| GB9523675D0 (en) * | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
| WO1999065897A1 (en) | 1998-06-19 | 1999-12-23 | Chiron Corporation | Inhibitors of glycogen synthase kinase 3 |
| GB9924862D0 (en) | 1999-10-20 | 1999-12-22 | Celltech Therapeutics Ltd | Chemical compounds |
| AU9502601A (en) * | 2000-09-06 | 2002-03-22 | Chiron Corp | Inhibitors of glycogen synthase kinase 3 |
| WO2002022605A1 (en) | 2000-09-15 | 2002-03-21 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US7129242B2 (en) | 2000-12-06 | 2006-10-31 | Signal Pharmaceuticals, Llc | Anilinopyrimidine derivatives as JNK pathway inhibitors and compositions and methods related thereto |
| US7122544B2 (en) | 2000-12-06 | 2006-10-17 | Signal Pharmaceuticals, Llc | Anilinopyrimidine derivatives as IKK inhibitors and compositions and methods related thereto |
| CA2441733A1 (en) | 2001-03-29 | 2002-10-10 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
| GB0107901D0 (en) * | 2001-03-29 | 2001-05-23 | Cyclacel Ltd | Anti-cancer compounds |
| WO2003030909A1 (en) | 2001-09-25 | 2003-04-17 | Bayer Pharmaceuticals Corporation | 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer |
| AU2003286876A1 (en) * | 2002-11-01 | 2004-06-07 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of jak and other protein kinases |
-
2003
- 2003-11-05 EP EP03778111A patent/EP1560824A1/en not_active Withdrawn
- 2003-11-05 AU AU2003286895A patent/AU2003286895A1/en not_active Abandoned
- 2003-11-05 WO PCT/US2003/035188 patent/WO2004041810A1/en not_active Ceased
- 2003-11-05 US US10/702,113 patent/US7348335B2/en not_active Expired - Fee Related
- 2003-11-05 CA CA002507406A patent/CA2507406A1/en not_active Abandoned
- 2003-11-05 JP JP2004550489A patent/JP2006508107A/ja active Pending
-
2010
- 2010-06-18 JP JP2010139840A patent/JP2010195838A/ja active Pending
- 2010-11-19 AU AU2010246324A patent/AU2010246324B2/en not_active Ceased
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