JP6077006B2 - ベンゾ複素環式化合物およびその使用 - Google Patents
ベンゾ複素環式化合物およびその使用 Download PDFInfo
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- JP6077006B2 JP6077006B2 JP2014551508A JP2014551508A JP6077006B2 JP 6077006 B2 JP6077006 B2 JP 6077006B2 JP 2014551508 A JP2014551508 A JP 2014551508A JP 2014551508 A JP2014551508 A JP 2014551508A JP 6077006 B2 JP6077006 B2 JP 6077006B2
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- 0 C*(C)(c1ccc(*)cc1)c(c(C(OO)=O)c1*)c(*)c(*=*)c1N Chemical compound C*(C)(c1ccc(*)cc1)c(c(C(OO)=O)c1*)c(*)c(*=*)c1N 0.000 description 15
- PFVVPDXPRXNIEZ-UHFFFAOYSA-N COC(c(c(Nc1ccccc1F)c1F)cc2c1nn[s]2)=O Chemical compound COC(c(c(Nc1ccccc1F)c1F)cc2c1nn[s]2)=O PFVVPDXPRXNIEZ-UHFFFAOYSA-N 0.000 description 2
- NFDVKCYUZSSBCE-UHFFFAOYSA-N C=CCC1(CC1)S(N(c(cc1[s]nnc1c1F)c1N1c(ccc(I)c2)c2F)C1=O)(=O)=O Chemical compound C=CCC1(CC1)S(N(c(cc1[s]nnc1c1F)c1N1c(ccc(I)c2)c2F)C1=O)(=O)=O NFDVKCYUZSSBCE-UHFFFAOYSA-N 0.000 description 1
- WXUDKXVLBAUFGF-UHFFFAOYSA-N COC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O Chemical compound COC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O WXUDKXVLBAUFGF-UHFFFAOYSA-N 0.000 description 1
- MIKWEZUYICJSFZ-UHFFFAOYSA-N COC(c(c(Nc(cccc1)c1F)c1F)cc(SCc(cc2)ccc2OC)c1N)=O Chemical compound COC(c(c(Nc(cccc1)c1F)c1F)cc(SCc(cc2)ccc2OC)c1N)=O MIKWEZUYICJSFZ-UHFFFAOYSA-N 0.000 description 1
- FQXMXSWGYNUGHY-UHFFFAOYSA-N COC(c(c(Nc1ccccc1F)c1F)cc(S)c1N)=O Chemical compound COC(c(c(Nc1ccccc1F)c1F)cc(S)c1N)=O FQXMXSWGYNUGHY-UHFFFAOYSA-N 0.000 description 1
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- KNLZGHPRJQYIMJ-UHFFFAOYSA-N COC(c(cc(c(N)c1F)SCc2ccccc2)c1Nc1ccccc1F)=O Chemical compound COC(c(cc(c(N)c1F)SCc2ccccc2)c1Nc1ccccc1F)=O KNLZGHPRJQYIMJ-UHFFFAOYSA-N 0.000 description 1
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- LCQFWCJNDNYMLZ-UHFFFAOYSA-N C[BrH][I-]C1=[I]CC1 Chemical compound C[BrH][I-]C1=[I]CC1 LCQFWCJNDNYMLZ-UHFFFAOYSA-N 0.000 description 1
- DWLJDFSKXUHTTP-UHFFFAOYSA-N C[O]=S(C1(CC=C)CC1)(Nc(c(Nc(ccc(I)c1)c1F)c1F)cc2c1nn[s]2)=O Chemical compound C[O]=S(C1(CC=C)CC1)(Nc(c(Nc(ccc(I)c1)c1F)c1F)cc2c1nn[s]2)=O DWLJDFSKXUHTTP-UHFFFAOYSA-N 0.000 description 1
- BNVYRBFYIBCXRD-UHFFFAOYSA-N Cc(cc1F)ccc1Nc(c(C(NOCCOC=C)=O)cc1c2nn[s]1)c2F Chemical compound Cc(cc1F)ccc1Nc(c(C(NOCCOC=C)=O)cc1c2nn[s]1)c2F BNVYRBFYIBCXRD-UHFFFAOYSA-N 0.000 description 1
- KKBPZAXGSWAZHA-UHFFFAOYSA-N O=C(Nc(c1c2F)cc3c2nn[s]3)N1c(c(F)c1)ccc1I Chemical compound O=C(Nc(c1c2F)cc3c2nn[s]3)N1c(c(F)c1)ccc1I KKBPZAXGSWAZHA-UHFFFAOYSA-N 0.000 description 1
- LPHRRQNLJIOSTB-UHFFFAOYSA-N O=C(c(c(Nc(c(Cl)c1)ccc1Br)c1F)cc2c1nc[s]2)NOCC1CC1 Chemical compound O=C(c(c(Nc(c(Cl)c1)ccc1Br)c1F)cc2c1nc[s]2)NOCC1CC1 LPHRRQNLJIOSTB-UHFFFAOYSA-N 0.000 description 1
- LCQLPQKOKHKAAP-UHFFFAOYSA-N O=C(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)NOCC1CC1 Chemical compound O=C(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)NOCC1CC1 LCQLPQKOKHKAAP-UHFFFAOYSA-N 0.000 description 1
- CCTFDOJAXGVCHD-UHFFFAOYSA-N O=C(c(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)NOCC1CC1 Chemical compound O=C(c(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)NOCC1CC1 CCTFDOJAXGVCHD-UHFFFAOYSA-N 0.000 description 1
- JUUINOLJRQVJJV-UHFFFAOYSA-N OC(c(c(Nc(cccc1)c1F)c1F)cc(Br)c1F)=O Chemical compound OC(c(c(Nc(cccc1)c1F)c1F)cc(Br)c1F)=O JUUINOLJRQVJJV-UHFFFAOYSA-N 0.000 description 1
- UQXIRWMDNLQNGM-UHFFFAOYSA-N OC(c(cc(c(F)c1F)OCc2ccccc2)c1Nc1ccccc1F)=O Chemical compound OC(c(cc(c(F)c1F)OCc2ccccc2)c1Nc1ccccc1F)=O UQXIRWMDNLQNGM-UHFFFAOYSA-N 0.000 description 1
- IVGFMRMTHAGJIO-UHFFFAOYSA-N OCC(CC1(CC1)S(Nc(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)(=O)=O)O Chemical compound OCC(CC1(CC1)S(Nc(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)(=O)=O)O IVGFMRMTHAGJIO-UHFFFAOYSA-N 0.000 description 1
- YYSGXYRHKZCROD-UHFFFAOYSA-N OCC(CC1(CCC1)S(Nc(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)(=O)=O)O Chemical compound OCC(CC1(CCC1)S(Nc(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)(=O)=O)O YYSGXYRHKZCROD-UHFFFAOYSA-N 0.000 description 1
- LMFCHUNAYDSVRN-UHFFFAOYSA-N OCCONC(c(c(NC(C(F)=C1)=CCC1Br)c1F)cc2c1nn[s]2)=O Chemical compound OCCONC(c(c(NC(C(F)=C1)=CCC1Br)c1F)cc2c1nn[s]2)=O LMFCHUNAYDSVRN-UHFFFAOYSA-N 0.000 description 1
- QQVGXTZHZFIFCV-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1Br)c1F)cc2c1nc[s]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1Br)c1F)cc2c1nc[s]2)=O QQVGXTZHZFIFCV-UHFFFAOYSA-N 0.000 description 1
- KALDBJONLIOQJS-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)=O KALDBJONLIOQJS-UHFFFAOYSA-N 0.000 description 1
- UFZJUVFSSINETF-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[s]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[s]2)=O UFZJUVFSSINETF-UHFFFAOYSA-N 0.000 description 1
- NCXQEKULAYAEMA-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O NCXQEKULAYAEMA-UHFFFAOYSA-N 0.000 description 1
- ZEVWANKJVWLMBU-UHFFFAOYSA-N OCCONC(c(c(Nc(ccc(C(F)(F)F)c1)c1F)c1F)cc2c1nc[o]2)=O Chemical compound OCCONC(c(c(Nc(ccc(C(F)(F)F)c1)c1F)c1F)cc2c1nc[o]2)=O ZEVWANKJVWLMBU-UHFFFAOYSA-N 0.000 description 1
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- Health & Medical Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
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- Hematology (AREA)
- Endocrinology (AREA)
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- Hospice & Palliative Care (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210014021 | 2012-01-17 | ||
| CN201210014021.X | 2012-01-17 | ||
| CN201210189087.2A CN103204827B (zh) | 2012-01-17 | 2012-06-08 | 作为蛋白激酶抑制剂的苯并噻二唑化合物及其制备方法和用途 |
| CN201210190520.4 | 2012-06-08 | ||
| CN201210190520.4A CN103204825B (zh) | 2012-01-17 | 2012-06-08 | 作为蛋白激酶抑制剂的苯并噻唑化合物及其制备方法和用途 |
| CN201210189086.8 | 2012-06-08 | ||
| CN201210189087.2 | 2012-06-08 | ||
| CN201210189086.8A CN103204822B (zh) | 2012-01-17 | 2012-06-08 | 作为蛋白激酶抑制剂的苯并噁唑化合物及其制备方法和用途 |
| PCT/CN2013/000037 WO2013107283A1 (en) | 2012-01-17 | 2013-01-16 | Benzoheterocyclic compounds and use thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015503597A JP2015503597A (ja) | 2015-02-02 |
| JP2015503597A5 JP2015503597A5 (https=) | 2016-03-10 |
| JP6077006B2 true JP6077006B2 (ja) | 2017-02-08 |
Family
ID=48752254
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014551508A Active JP6077006B2 (ja) | 2012-01-17 | 2013-01-16 | ベンゾ複素環式化合物およびその使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9290468B2 (https=) |
| EP (1) | EP2804855B1 (https=) |
| JP (1) | JP6077006B2 (https=) |
| CN (3) | CN103204827B (https=) |
| CA (1) | CA2897259C (https=) |
| NZ (1) | NZ627631A (https=) |
| WO (1) | WO2013107283A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104710417B (zh) * | 2013-12-11 | 2020-09-08 | 上海科州药物研发有限公司 | 氮杂吲哚类衍生物及其合成方法 |
| CN105384738B (zh) * | 2014-08-21 | 2017-08-29 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
| CN105859543A (zh) * | 2016-05-06 | 2016-08-17 | 蚌埠中实化学技术有限公司 | 一种2,6-二氟-4-溴苯甲酰氯的制备方法 |
| CN111205244B (zh) * | 2018-11-22 | 2023-08-18 | 上海科技大学 | 噻唑并环类化合物、其制备方法、中间体和应用 |
| US20220143049A1 (en) | 2019-03-21 | 2022-05-12 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| EP4054579A1 (en) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| CN113440616A (zh) * | 2020-03-25 | 2021-09-28 | 上海科州药物研发有限公司 | Ras或raf突变型癌症的联合疗法 |
| PE20260035A1 (es) * | 2023-02-10 | 2026-01-09 | Shanghai Kechow Pharma Inc | Polimorfo como inhibidor de la proteina quinasa mek, metodo de preparacion y uso del mismo |
| WO2025073765A1 (en) | 2023-10-03 | 2025-04-10 | Institut National de la Santé et de la Recherche Médicale | Methods of prognosis and treatment of patients suffering from melanoma |
| WO2025242163A1 (zh) * | 2024-05-23 | 2025-11-27 | 上海科州药物股份有限公司 | 蛋白激酶mek抑制剂的盐及其用途 |
| WO2025261499A1 (zh) * | 2024-06-20 | 2025-12-26 | 上海科州药物股份有限公司 | 蛋白激酶Mek抑制剂苯并噻唑的颗粒药物组合物 |
| CN120463660A (zh) * | 2024-09-30 | 2025-08-12 | 上海科州药物股份有限公司 | 大规模制备妥拉美替尼及其中间体的方法 |
Family Cites Families (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA73073C2 (uk) | 1997-04-03 | 2005-06-15 | Уайт Холдінгз Корпорейшн | Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція |
| CA2290509A1 (en) | 1997-07-01 | 1999-01-14 | Warner-Lambert Company | 2-(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as mek inhibitors |
| NZ501276A (en) | 1997-07-01 | 2000-10-27 | Warner Lambert Co | 4-bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors in treating proliferative disorders |
| US6120451A (en) | 1998-12-31 | 2000-09-19 | General Electric Company | Ultrasound color flow display optimization by adjustment of threshold |
| HUP0105092A3 (en) | 1999-01-13 | 2003-12-29 | Warner Lambert Co | 1-heterocycle substituted diarylamines and medicaments containing them |
| CA2348236A1 (en) | 1999-01-13 | 2000-07-20 | Stephen Douglas Barrett | 4-arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective mek inhibitors |
| EP1144372B1 (en) | 1999-01-13 | 2005-11-30 | Warner-Lambert Company Llc | Sulphohydroxamic acids and sulphohydroxamates and their use as mek inhibitors |
| EP1150950A2 (en) | 1999-01-13 | 2001-11-07 | Warner-Lambert Company | Anthranilic acid derivatives |
| CA2355470C (en) * | 1999-01-13 | 2008-09-30 | Warner-Lambert Company | Benzoheterocycles and their use as mek inhibitors |
| JP2000204079A (ja) * | 1999-01-13 | 2000-07-25 | Warner Lambert Co | ジアリ―ルアミン |
| GB9910577D0 (en) | 1999-05-08 | 1999-07-07 | Zeneca Ltd | Chemical compounds |
| CA2377092A1 (en) * | 1999-07-16 | 2001-01-25 | Warner-Lambert Company | Method for treating chronic pain using mek inhibitors |
| BR0109188A (pt) | 2000-03-15 | 2003-03-18 | Warner Lambert Co | Diarilaminas 5-amida substituìdas como inibidores de mex |
| DZ3401A1 (fr) | 2000-07-19 | 2002-01-24 | Warner Lambert Co | Esters oxygenes d'acides 4-iodophenylamino benzhydroxamiques |
| US7235537B2 (en) * | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
| EP1482944A4 (en) | 2002-03-13 | 2006-04-19 | Array Biopharma Inc | NZ ALKYL BENZIMIDAZOLE DERIVATIVES AS MEK INHIBITORS |
| SG2013013339A (en) * | 2002-03-13 | 2014-12-30 | Array Biopharma Inc | N3 alkylated benzimidazole derivatives as mek inhibitors |
| US20050004186A1 (en) * | 2002-12-20 | 2005-01-06 | Pfizer Inc | MEK inhibiting compounds |
| WO2005000818A1 (en) | 2003-06-27 | 2005-01-06 | Warner-Lambert Company Llc | 5-substituted-4-`(substituted phenyl)!amino!-2-pyridone deviatives for use as mek inhibitors |
| WO2005007616A1 (en) | 2003-07-23 | 2005-01-27 | Warner-Lambert Company Llc | Diphenylamino ketone derivatives as mek inhibitors |
| CA2532067C (en) | 2003-07-24 | 2010-12-21 | Stephen Douglas Barrett | N-methyle-substituted benzamidazoles |
| US7144907B2 (en) * | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
| WO2005046665A1 (en) | 2003-11-13 | 2005-05-26 | Warner-Lambert Company Llc | Combination chemotherapy comprising a mek inhibitor and a erbb1/2 receptor inhibitor |
| CA2546353A1 (en) | 2003-11-19 | 2005-06-09 | Array Biopharma Inc. | Bicyclic inhibitors of mek and methods of use thereof |
| SG177981A1 (en) | 2005-05-18 | 2012-02-28 | Array Biopharma Inc | 4-(phenylamino)-6-oxo-1, 6-dihydropyridazine-3-carboxamide derivatives as mek inhibitors for the treatment of hyperproliferative diseases |
| WO2006134469A1 (en) | 2005-06-14 | 2006-12-21 | Warner-Lambert Company Llc | Methods of preparing mek inhibitor |
| FR2887882B1 (fr) | 2005-07-01 | 2007-09-07 | Sanofi Aventis Sa | Derives de pyrido[2,3-d] pyrimidine, leur preparation, leur application en therapeutique |
| MX2008002114A (es) | 2005-07-21 | 2008-04-17 | Ardea Biosciences Inc | Inhibidores de n-(arilamino)-sulfonamida de mek. |
| US8101799B2 (en) | 2005-07-21 | 2012-01-24 | Ardea Biosciences | Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK |
| HRP20110498T1 (hr) | 2005-10-07 | 2011-08-31 | Exelixis | Azetidini kao inhibitori mek za liječenje proliferativnih bolesti |
| EP1966155A1 (en) | 2005-12-21 | 2008-09-10 | AstraZeneca AB | Tosylate salt of 6- (4-br0m0-2-chl0r0phenylamin0) -7-fluoro-n- (2-hydroxyethoxy) -3-methyl-3h-benzimi dazole- 5 - carboxamide , mek inhibitor useful in the treatment of cancer |
| US7842836B2 (en) | 2006-04-11 | 2010-11-30 | Ardea Biosciences | N-aryl-N'alkyl sulfamides as MEK inhibitors |
| WO2007121154A2 (en) * | 2006-04-11 | 2007-10-25 | Janssen Pharmaceutica, N.V. | Substituted benzothiazole kinase inhibitors |
| MX2008013097A (es) | 2006-04-18 | 2008-10-27 | Ardea Biosciences Inc | Piridona sulfonamidas y piridona sulfamidas como inhibidores de metiletilcetona. |
| CN101528231A (zh) | 2006-08-16 | 2009-09-09 | 埃克塞利希斯股份有限公司 | 在癌症的治疗中使用pi3k和mek调控剂 |
| WO2008076415A1 (en) | 2006-12-14 | 2008-06-26 | Exelixis, Inc. | Methods of using mek inhibitors |
| GB0625691D0 (en) | 2006-12-22 | 2007-01-31 | Astrazeneca Ab | Combination product |
| FR2911138B1 (fr) * | 2007-01-05 | 2009-02-20 | Sanofi Aventis Sa | Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk |
| MX2009007661A (es) | 2007-01-19 | 2009-12-14 | Ardea Biosciences Inc | Inhibidores de mek. |
| WO2008120004A1 (en) | 2007-04-02 | 2008-10-09 | Astrazeneca Ab | Combination of a mek- inhibitor and a b-raf inhibitor for the treatment of cancer |
| WO2008124085A2 (en) | 2007-04-03 | 2008-10-16 | Exelixis, Inc. | Methods of using combinations of mek and jak-2 inhibitors |
| US20100130519A1 (en) | 2007-04-13 | 2010-05-27 | Stephen Robert Wedge | Combination therapy comprising azd2171 and azd6244 or mek-inhibitor ii |
| US7960567B2 (en) | 2007-05-02 | 2011-06-14 | Amgen Inc. | Compounds and methods useful for treating asthma and allergic inflammation |
| CA2688823A1 (en) | 2007-05-21 | 2008-11-27 | Sgx Pharmaceuticals, Inc. | Heterocyclic kinase modulators |
| FR2918785B1 (fr) | 2007-07-13 | 2009-11-13 | Lemer Prot Anti X Par Abrevati | Materiau radioattenuateur, et procede pour l'obtention d'un tel materiau |
| UA99731C2 (ru) | 2007-07-30 | 2012-09-25 | Ардеа Биосайенсис, Инк | Кристаллические полиморфные формы n-(ариламино)сульфонамидов как ингибиторы мэк, композиция (варианты) и применение |
| EP2231281A2 (en) | 2007-12-12 | 2010-09-29 | AstraZeneca AB | Combination comprising a mek inhibitor and an aurora kinase inhibitor |
| GB0801081D0 (en) | 2008-01-21 | 2008-02-27 | Ucb Pharma Sa | Therapeutic agents |
| GB0801080D0 (en) | 2008-01-21 | 2008-02-27 | Ucb Pharma Sa | Therapeutic agents |
| WO2009093008A1 (en) | 2008-01-21 | 2009-07-30 | Ucb Pharma S.A. | Thieno-pyridine derivatives as mek inhibitors |
| GB0811304D0 (en) | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
| CA2781218A1 (en) | 2009-12-08 | 2011-06-16 | Novartis Ag | Heterocyclic sulfonamide derivatives |
| 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 |
| FR2967672B1 (fr) | 2010-11-22 | 2012-12-28 | Sanofi Aventis | Derives de nitrobenzothiazoles, leur preparation et leurs applications therapeutiques |
| BR112013027096A2 (pt) | 2011-04-21 | 2016-12-27 | Gilead Sciences Inc | compostos de benzotiazol e seu uso farmacêutico |
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| EP2804855B1 (en) | 2017-09-20 |
| CN103204827B (zh) | 2014-12-03 |
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| HK1203486A1 (en) | 2015-10-30 |
| US9290468B2 (en) | 2016-03-22 |
| US20160235721A1 (en) | 2016-08-18 |
| JP2015503597A (ja) | 2015-02-02 |
| CN103204825A (zh) | 2013-07-17 |
| EP2804855A1 (en) | 2014-11-26 |
| AU2013201455A8 (en) | 2016-04-14 |
| WO2013107283A1 (en) | 2013-07-25 |
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| AU2013201455B2 (en) | 2015-07-23 |
| AU2013201455C1 (en) | 2016-01-21 |
| CA2897259C (en) | 2019-05-07 |
| AU2013201455A1 (en) | 2013-08-01 |
| CA2897259A1 (en) | 2013-07-25 |
| US9937158B2 (en) | 2018-04-10 |
| CN103204825B (zh) | 2015-03-04 |
| CN103204827A (zh) | 2013-07-17 |
| EP2804855A4 (en) | 2015-07-29 |
| NZ627631A (en) | 2016-10-28 |
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