JP2013545718A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013545718A5 JP2013545718A5 JP2013524677A JP2013524677A JP2013545718A5 JP 2013545718 A5 JP2013545718 A5 JP 2013545718A5 JP 2013524677 A JP2013524677 A JP 2013524677A JP 2013524677 A JP2013524677 A JP 2013524677A JP 2013545718 A5 JP2013545718 A5 JP 2013545718A5
- Authority
- JP
- Japan
- Prior art keywords
- ring
- substituted
- optionally substituted
- salt
- group
- 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 description 13
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims 19
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 14
- 150000003839 salts Chemical class 0.000 claims 14
- 125000003118 aryl group Chemical group 0.000 claims 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 6
- 125000002619 bicyclic group Chemical group 0.000 claims 6
- 239000003814 drug Substances 0.000 claims 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 4
- 125000006574 non-aromatic ring group Chemical group 0.000 claims 4
- 208000008589 Obesity Diseases 0.000 claims 3
- 206010012601 diabetes mellitus Diseases 0.000 claims 3
- 235000020824 obesity Nutrition 0.000 claims 3
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 230000005494 condensation Effects 0.000 claims 2
- 238000009833 condensation Methods 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 2
- 230000000069 prophylactic effect Effects 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- 229940121373 acetyl-coa carboxylase inhibitor Drugs 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- ADHDEZRLSWZHKE-LBPRGKRZSA-N n-[(2s)-1-[6-(6-ethoxy-1,3-benzoxazol-2-yl)pyridin-3-yl]oxypropan-2-yl]acetamide Chemical compound O1C2=CC(OCC)=CC=C2N=C1C1=CC=C(OC[C@H](C)NC(C)=O)C=N1 ADHDEZRLSWZHKE-LBPRGKRZSA-N 0.000 claims 1
- CBRJFLKXQUUGQV-LBPRGKRZSA-N n-[(2s)-1-[6-[6-(cyclopropylmethoxy)-1,3-benzoxazol-2-yl]-5-fluoropyridin-3-yl]oxypropan-2-yl]acetamide Chemical compound FC1=CC(OC[C@H](C)NC(C)=O)=CN=C1C(OC1=C2)=NC1=CC=C2OCC1CC1 CBRJFLKXQUUGQV-LBPRGKRZSA-N 0.000 claims 1
- ZAAOFSTVMJFFPI-ZDUSSCGKSA-N n-[(2s)-1-[6-[6-(cyclopropylmethoxy)-1,3-benzoxazol-2-yl]pyridin-3-yl]oxypropan-2-yl]acetamide Chemical compound N1=CC(OC[C@H](C)NC(C)=O)=CC=C1C(OC1=C2)=NC1=CC=C2OCC1CC1 ZAAOFSTVMJFFPI-ZDUSSCGKSA-N 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 0 CC*=N*(C)C Chemical compound CC*=N*(C)C 0.000 description 7
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 6
- -1 5 - {[ (2S) -2- aminopropyl] oxy} pyridin-2-yl Chemical group 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000012267 brine Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ALJQVIZVWCKBIQ-UHFFFAOYSA-N 6-[6-(methoxymethoxy)-2-methyl-3h-1-benzofuran-2-yl]pyridin-3-ol Chemical compound O1C2=CC(OCOC)=CC=C2CC1(C)C1=CC=C(O)C=N1 ALJQVIZVWCKBIQ-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000002953 preparative HPLC Methods 0.000 description 2
- CZZPSVORNFBYEX-UHFFFAOYSA-N 3,3-diethylpentan-1-amine Chemical compound CCC(CC)(CC)CCN CZZPSVORNFBYEX-UHFFFAOYSA-N 0.000 description 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 1
- IBKFLJRJFOGTOQ-UHFFFAOYSA-N C(C)(=O)N.BrCC1CC1 Chemical compound C(C)(=O)N.BrCC1CC1 IBKFLJRJFOGTOQ-UHFFFAOYSA-N 0.000 description 1
- OAYCSWBEXSUQAY-UHFFFAOYSA-N C(C)(=O)OC(C)=O.C(C)(=O)N Chemical compound C(C)(=O)OC(C)=O.C(C)(=O)N OAYCSWBEXSUQAY-UHFFFAOYSA-N 0.000 description 1
- CSWGKBFMCBXHNL-UHFFFAOYSA-N CC1NN(C=CC(C)=C2)C2=C1 Chemical compound CC1NN(C=CC(C)=C2)C2=C1 CSWGKBFMCBXHNL-UHFFFAOYSA-N 0.000 description 1
- DVZVWYAUBOMCJA-UHFFFAOYSA-N CC1Oc2ccc(C)cc2N1 Chemical compound CC1Oc2ccc(C)cc2N1 DVZVWYAUBOMCJA-UHFFFAOYSA-N 0.000 description 1
- GYCGFNPVXKJNTL-UHFFFAOYSA-N Cc1c[n](ccc(C)c2)c2n1 Chemical compound Cc1c[n](ccc(C)c2)c2n1 GYCGFNPVXKJNTL-UHFFFAOYSA-N 0.000 description 1
- HMMPHXCOTBASBC-UHFFFAOYSA-N Cc1cc2n[nH]cc2cc1 Chemical compound Cc1cc2n[nH]cc2cc1 HMMPHXCOTBASBC-UHFFFAOYSA-N 0.000 description 1
- DDJNVLANJKUROF-UHFFFAOYSA-N Cc1n[n](CCC(C)=C2)c2c1 Chemical compound Cc1n[n](CCC(C)=C2)c2c1 DDJNVLANJKUROF-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- NIZHERJWXFHGGU-UHFFFAOYSA-N isocyanato(trimethyl)silane Chemical compound C[Si](C)(C)N=C=O NIZHERJWXFHGGU-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- OKMJCVKFQXNEDD-AWEZNQCLSA-N tert-butyl n-[(2s)-1-[4-(6-ethoxy-3-fluoropyrazolo[1,5-a]pyridin-2-yl)-3-fluorophenoxy]propan-2-yl]carbamate Chemical compound N=1N2C=C(OCC)C=CC2=C(F)C=1C1=CC=C(OC[C@H](C)NC(=O)OC(C)(C)C)C=C1F OKMJCVKFQXNEDD-AWEZNQCLSA-N 0.000 description 1
- MHAQEPQMTBZZKV-FXIRQEPWSA-N tert-butyl n-[(2s)-1-[6-[6-(methoxymethoxy)-2-methyl-3h-1-benzofuran-2-yl]pyridin-3-yl]oxypropan-2-yl]carbamate Chemical compound O1C2=CC(OCOC)=CC=C2CC1(C)C1=CC=C(OC[C@H](C)NC(=O)OC(C)(C)C)C=N1 MHAQEPQMTBZZKV-FXIRQEPWSA-N 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013524677A JP5824517B2 (ja) | 2010-11-30 | 2011-11-29 | 二環性化合物 |
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010266097 | 2010-11-30 | ||
| JP2010266097 | 2010-11-30 | ||
| JP2011175330 | 2011-08-10 | ||
| JP2011175330 | 2011-08-10 | ||
| PCT/JP2011/078010 WO2012074126A1 (en) | 2010-11-30 | 2011-11-29 | Bicyclic compound |
| JP2013524677A JP5824517B2 (ja) | 2010-11-30 | 2011-11-29 | 二環性化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013545718A JP2013545718A (ja) | 2013-12-26 |
| JP2013545718A5 true JP2013545718A5 (OSRAM) | 2014-08-21 |
| JP5824517B2 JP5824517B2 (ja) | 2015-11-25 |
Family
ID=45418740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013524677A Expired - Fee Related JP5824517B2 (ja) | 2010-11-30 | 2011-11-29 | 二環性化合物 |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US8729102B2 (OSRAM) |
| EP (1) | EP2649062B1 (OSRAM) |
| JP (1) | JP5824517B2 (OSRAM) |
| KR (1) | KR20140001965A (OSRAM) |
| CN (1) | CN103347872B (OSRAM) |
| AR (1) | AR084032A1 (OSRAM) |
| AU (1) | AU2011337565A1 (OSRAM) |
| BR (1) | BR112013013417A2 (OSRAM) |
| CA (1) | CA2819400A1 (OSRAM) |
| CL (1) | CL2013001520A1 (OSRAM) |
| CO (1) | CO6751239A2 (OSRAM) |
| CR (1) | CR20130281A (OSRAM) |
| DO (1) | DOP2013000118A (OSRAM) |
| EA (1) | EA201390794A1 (OSRAM) |
| EC (1) | ECSP13012719A (OSRAM) |
| ES (1) | ES2536319T3 (OSRAM) |
| MA (1) | MA34713B1 (OSRAM) |
| MX (1) | MX2013006113A (OSRAM) |
| PE (1) | PE20140161A1 (OSRAM) |
| PH (1) | PH12013501099A1 (OSRAM) |
| SG (1) | SG190925A1 (OSRAM) |
| TW (1) | TW201242951A (OSRAM) |
| UY (1) | UY33756A (OSRAM) |
| WO (1) | WO2012074126A1 (OSRAM) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW201206911A (en) | 2010-04-27 | 2012-02-16 | Takeda Pharmaceutical | Bicyclic compound |
| JPWO2013061962A1 (ja) | 2011-10-24 | 2015-04-02 | 武田薬品工業株式会社 | 二環性化合物 |
| US9580407B2 (en) | 2012-12-07 | 2017-02-28 | Merck Sharp & Dohme Corp. | Regioselective N-2 arylation of indazoles |
| PL403149A1 (pl) * | 2013-03-14 | 2014-09-15 | Celon Pharma Spółka Akcyjna | Nowe związki pochodne pirazolilobenzo[d]imidazolu |
| JP6434498B2 (ja) * | 2013-05-10 | 2018-12-05 | ギリアド アポロ， エルエルシー | Ａｃｃ阻害剤及びその使用 |
| HK1221420A1 (zh) | 2013-05-10 | 2017-06-02 | Gilead Apollo, Inc. | Acc抑制剂和其用途 |
| MX2015015417A (es) | 2013-05-10 | 2016-06-21 | Nimbus Apollo Inc | Inhibidores de acetil-coa carboxilasa (acc) y usos de los mismos. |
| KR20160005364A (ko) | 2013-05-10 | 2016-01-14 | 님버스 아폴로, 인코포레이티드 | Acc 억제제 및 이의 용도 |
| WO2015036892A1 (en) | 2013-09-12 | 2015-03-19 | Pfizer Inc. | Use of acetyl-coa carboxylase inhibitors for treating acne vulgaris |
| EA201690888A1 (ru) | 2013-11-14 | 2016-10-31 | Кадила Хелзкэр Лимитед | Новые гетероциклические соединения |
| KR102523430B1 (ko) | 2014-08-04 | 2023-04-19 | 누에볼루션 에이/에스 | 염증성, 대사성, 종양성 및 자가면역성 질환의 치료에 유용한 피리미딘의 임의적 융합 헤테로시클릴-치환 유도체 |
| CN104193731B (zh) * | 2014-08-27 | 2017-03-15 | 广东东阳光药业有限公司 | 一种脲取代联苯类化合物及其组合物及用途 |
| EA035646B1 (ru) * | 2014-08-29 | 2020-07-21 | Сиэйчдиай Фаундэйшн, Инк. | Зонды для визуализации белка хантингтина |
| JP2016079168A (ja) * | 2014-10-17 | 2016-05-16 | 塩野義製薬株式会社 | ９員縮合環誘導体 |
| CN104447725B (zh) * | 2014-10-22 | 2018-02-02 | 浙江大学 | 一种手性含亚胺吡啶噁唑啉的化合物及其制备方法 |
| US9586949B2 (en) | 2015-02-09 | 2017-03-07 | Incyte Corporation | Aza-heteroaryl compounds as PI3K-gamma inhibitors |
| AU2016332021A1 (en) | 2015-09-29 | 2018-04-19 | Oncotherapy Science, Inc. | Bicyclic compound and use thereof for inhibiting SUV39H2 |
| CN105601626A (zh) * | 2015-11-04 | 2016-05-25 | 浙江大学 | 一种含2-取代噁唑啉衍生物的制备方法 |
| AR106595A1 (es) | 2015-11-06 | 2018-01-31 | Incyte Corp | COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE PI3K-g |
| EP3792256B1 (en) | 2016-01-05 | 2024-10-23 | Incyte Corporation | Pyridine compounds as pi3k-gamma inhibitors |
| TW201803871A (zh) | 2016-06-24 | 2018-02-01 | 英塞特公司 | 作為ＰＩ３Ｋ-γ抑制劑之雜環化合物 |
| CN110753684A (zh) | 2017-04-24 | 2020-02-04 | 特沙诺有限公司 | 尼拉帕利的制造方法 |
| MX2020003862A (es) | 2017-10-18 | 2020-08-13 | Incyte Corp | Derivados condensados de imidazol sustituidos por grupos hidroxi terciarios como inhibidores de fosfoinositido 3-cinasas gamma (pi3k-gamma). |
| CR20250050A (es) | 2018-09-05 | 2025-03-19 | Incyte Corp | Formas cristalinas de un inhibidor de fosfoinositida 3–quinasa (pi3k) (divisional 2021-0165) |
| UY38994A (es) | 2019-12-20 | 2021-07-30 | Nuevolution As | Compuestos activos frente a receptores nucleares |
| US11447479B2 (en) | 2019-12-20 | 2022-09-20 | Nuevolution A/S | Compounds active towards nuclear receptors |
| EP4126875A1 (en) | 2020-03-31 | 2023-02-08 | Nuevolution A/S | Compounds active towards nuclear receptors |
| AU2021245397A1 (en) | 2020-03-31 | 2022-10-20 | Nuevolution A/S | Compounds active towards nuclear receptors |
| EP4434520A4 (en) | 2021-11-19 | 2025-10-29 | Shionogi & Co | PHARMACEUTICAL PRODUCT FOR THE TREATMENT OF HEART DISEASE OR SKELETAL MUSCLE DISEASE |
| AR129265A1 (es) | 2022-05-12 | 2024-08-07 | Syngenta Crop Protection Ag | Compuestos de alcoxi-heteroaril-carboxamida o tioamida |
| WO2024033374A1 (en) | 2022-08-11 | 2024-02-15 | Syngenta Crop Protection Ag | Novel arylcarboxamide or arylthioamide compounds |
| CN120476107A (zh) | 2022-12-15 | 2025-08-12 | 先正达农作物保护股份公司 | 可用作杀有害生物剂的新型的二环-甲酰胺化合物 |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997010224A1 (en) | 1995-09-13 | 1997-03-20 | Takeda Chemical Industries, Ltd. | Benzoxazepine compounds, their production and use as lipid lowering agents |
| JP2002501503A (ja) * | 1997-04-30 | 2002-01-15 | イーライ・リリー・アンド・カンパニー | 抗血栓症剤 |
| AR035016A1 (es) | 1999-08-25 | 2004-04-14 | Takeda Chemical Industries Ltd | Composicion de azol promotor de produccion/secrecion de neurotrofina, compuesto prodroga del mismo, composicion farmaceutica que lo comprende y uso del mismo para preparar esta ultima. |
| EP1285651B1 (en) | 2000-04-28 | 2010-09-01 | Takeda Pharmaceutical Company Limited | Melanin concentrating hormone antagonists |
| EP1283199A4 (en) | 2000-05-16 | 2003-12-17 | Takeda Chemical Industries Ltd | MELANINE CONCENTRATING HORMONE ANTAGONISTS |
| AU2001269531A1 (en) | 2000-07-17 | 2002-01-30 | Takeda Chemical Industries Ltd. | Sulfone derivatives, process for their production and use thereof |
| DK1542997T3 (da) * | 2002-07-24 | 2012-06-25 | Dermira Canada Inc | Pyrazolylbenzothiazolderivater og deres anvendelse som terapeutiske midler |
| PL376733A1 (pl) | 2002-11-01 | 2006-01-09 | Takeda Pharmaceutical Company Limited | Środek do zapobiegania lub leczenia neuropatii |
| AU2003277576A1 (en) | 2002-11-08 | 2004-06-07 | Takeda Pharmaceutical Company Limited | Receptor function controlling agent |
| EP1564213A4 (en) | 2002-11-22 | 2009-05-27 | Takeda Pharmaceutical | IMIDAZOLE DERIVATIVE, METHOD FOR THE PRODUCTION AND USE THEREOF |
| WO2004106276A1 (ja) | 2003-05-30 | 2004-12-09 | Takeda Pharmaceutical Company Limited | 縮合環化合物 |
| EP1669352A4 (en) | 2003-09-30 | 2008-12-17 | Takeda Pharmaceutical | THIAZOLINE DERIVATIVE AND ITS USE |
| US7820673B2 (en) | 2003-12-17 | 2010-10-26 | Takeda Pharmaceutical Company Limited | Urea derivative, process for producing the same, and use |
| WO2005063729A1 (en) | 2003-12-25 | 2005-07-14 | Takeda Pharmaceutical Company Limited | 3-(4-benzyloxyphenyl)propanoic acid derivatives |
| JP4855777B2 (ja) | 2003-12-26 | 2012-01-18 | 武田薬品工業株式会社 | フェニルプロパン酸誘導体 |
| WO2005087710A1 (ja) | 2004-03-15 | 2005-09-22 | Takeda Pharmaceutical Company Limited | アミノフェニルプロパン酸誘導体 |
| US7517910B2 (en) | 2004-03-30 | 2009-04-14 | Takeda Pharmaceutical Company Limited | Alkoxyphenylpropanoic acid derivatives |
| TWI396686B (zh) | 2004-05-21 | 2013-05-21 | Takeda Pharmaceutical | 環狀醯胺衍生物、以及其製品和用法 |
| US8957070B2 (en) | 2005-04-20 | 2015-02-17 | Takeda Pharmaceutical Company Limited | Glucokinase activator compounds, methods of activating glucokinase and methods of treating diabetes and obesity |
| EP1911738A4 (en) | 2005-07-29 | 2009-12-16 | Takeda Pharmaceutical | COMPOUND OF PHENOXYALKANOIC ACID |
| WO2007013689A1 (ja) | 2005-07-29 | 2007-02-01 | Takeda Pharmaceutical Company Limited | シクロプロパンカルボン酸化合物 |
| AU2006277231A1 (en) | 2005-08-10 | 2007-02-15 | Takeda Pharmaceutical Company Limited | Therapeutic agent for diabetes |
| JP2007063225A (ja) | 2005-09-01 | 2007-03-15 | Takeda Chem Ind Ltd | イミダゾピリジン化合物 |
| EP1996567B1 (en) * | 2006-02-15 | 2013-09-18 | AbbVie Inc. | Novel acetyl-coa carboxylase (acc) inhibitors and their use in diabetes, obesity and metabolic syndrome |
| JO2969B1 (en) | 2006-06-27 | 2016-03-15 | تاكيدا فارماسويتيكال كمبني ليمتد | Welded circular compounds |
| EP2077267A4 (en) | 2006-10-18 | 2010-04-07 | Takeda Pharmaceutical | CONDENSED HETEROCYCLIC COMPOUND |
| NZ576570A (en) | 2006-10-19 | 2010-11-26 | Takeda Pharmaceutical | 7-sulfonylamino-2-thiazol and 2-thiadiazol -indole compounds |
| EP2128138A1 (en) | 2007-01-29 | 2009-12-02 | Takeda Pharmaceutical Company Limited | Pyrazole compound |
| CN101646653A (zh) | 2007-02-09 | 2010-02-10 | 武田药品工业株式会社 | 作为ppar-y的部分激动剂的稠环化合物 |
| JPWO2008136428A1 (ja) | 2007-04-27 | 2010-07-29 | 武田薬品工業株式会社 | 含窒素５員複素環化合物 |
| US20110301155A1 (en) | 2007-06-19 | 2011-12-08 | Tsuneo Yasuma | Indazole compounds for activating glucokinase |
| JP5535931B2 (ja) | 2008-10-27 | 2014-07-02 | 武田薬品工業株式会社 | 二環性化合物 |
| US8927576B2 (en) * | 2009-04-06 | 2015-01-06 | PTC Therpeutics, Inc. | HCV inhibitor and therapeutic agent combinations |
| TW201206911A (en) | 2010-04-27 | 2012-02-16 | Takeda Pharmaceutical | Bicyclic compound |
| WO2012108478A1 (ja) | 2011-02-09 | 2012-08-16 | 武田薬品工業株式会社 | 単環化合物 |
-
2011
- 2011-11-29 AR ARP110104436A patent/AR084032A1/es not_active Application Discontinuation
- 2011-11-29 EP EP11802168.2A patent/EP2649062B1/en active Active
- 2011-11-29 US US13/306,069 patent/US8729102B2/en not_active Expired - Fee Related
- 2011-11-29 BR BR112013013417A patent/BR112013013417A2/pt not_active IP Right Cessation
- 2011-11-29 SG SG2013041546A patent/SG190925A1/en unknown
- 2011-11-29 KR KR1020137016850A patent/KR20140001965A/ko not_active Withdrawn
- 2011-11-29 PH PH1/2013/501099A patent/PH12013501099A1/en unknown
- 2011-11-29 CN CN201180066388.XA patent/CN103347872B/zh not_active Expired - Fee Related
- 2011-11-29 WO PCT/JP2011/078010 patent/WO2012074126A1/en not_active Ceased
- 2011-11-29 EA EA201390794A patent/EA201390794A1/ru unknown
- 2011-11-29 MX MX2013006113A patent/MX2013006113A/es not_active Application Discontinuation
- 2011-11-29 ES ES11802168.2T patent/ES2536319T3/es active Active
- 2011-11-29 CA CA2819400A patent/CA2819400A1/en not_active Abandoned
- 2011-11-29 UY UY0001033756A patent/UY33756A/es not_active Application Discontinuation
- 2011-11-29 PE PE2013001328A patent/PE20140161A1/es not_active Application Discontinuation
- 2011-11-29 JP JP2013524677A patent/JP5824517B2/ja not_active Expired - Fee Related
- 2011-11-29 AU AU2011337565A patent/AU2011337565A1/en not_active Abandoned
- 2011-11-29 TW TW100143674A patent/TW201242951A/zh unknown
-
2013
- 2013-05-29 CL CL2013001520A patent/CL2013001520A1/es unknown
- 2013-05-29 DO DO2013000118A patent/DOP2013000118A/es unknown
- 2013-06-05 MA MA35965A patent/MA34713B1/fr unknown
- 2013-06-11 CR CR20130281A patent/CR20130281A/es not_active Application Discontinuation
- 2013-06-24 CO CO13149620A patent/CO6751239A2/es not_active Application Discontinuation
- 2013-06-25 EC ECSP13012719 patent/ECSP13012719A/es unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013545718A5 (OSRAM) | ||
| JP5254228B2 (ja) | バニロイド受容体アンタゴニストとしての、新規化合物、その異性体またはその薬学的に許容される塩；並びにそれを含む医薬組成物 | |
| KR102662215B1 (ko) | 치환된 피라졸로(1,5-a)피리미딘 및 의학적 장애의 치료에서의 그의 용도 | |
| AU2016303540B2 (en) | Novel compounds as ROR gamma modulators | |
| JP2016535784A5 (OSRAM) | ||
| CA2914997C (en) | 4-alkynyl imidazole derivative and medicine comprising same as active ingredient | |
| WO2004007439A1 (ja) | ビアリール誘導体 | |
| JP2016512823A5 (OSRAM) | ||
| WO2019141179A1 (zh) | 吡啶酮衍生物、其组合物及作为抗流感病毒药物的应用 | |
| WO2014125426A1 (en) | Trisubstituted heterocyclic derivatives as ror gamma modulators | |
| AU2012337781A1 (en) | Dihydroxy aromatic heterocyclic compound | |
| JP2016027019A (ja) | 縮合複素環化合物の製造方法 | |
| JP2015503595A5 (OSRAM) | ||
| JP6250862B2 (ja) | アルドステロン合成酵素阻害薬 | |
| JP5091663B2 (ja) | 新規なアントラニル酸誘導体またはその塩 | |
| TW201725192A (zh) | 芳香族醯胺衍生物之製造方法 | |
| JP2017534653A (ja) | ブロモドメイン及びエキストラ末端タンパク質の阻害のための方法及び組成物 | |
| JP2018535260A (ja) | キナーゼ阻害剤およびその中間体の調製方法 | |
| JP2020533328A (ja) | ベンゼン縮合複素環誘導体およびその医薬組成物 | |
| KR20180002796A (ko) | 시클로프로판 카르복실산 유도체 및 이의 의약 용도 | |
| AU2015247575B2 (en) | Polycyclic hERG activators | |
| AU2021337476B2 (en) | Novel biaryl derivative useful as diacylglycerol acyltransferase 2 inhibitor, and use thereof | |
| US6809204B2 (en) | Processes for the preparation of substituted isoxazoles and 2-isoxazolines | |
| EP4263540A1 (en) | Nitrogen containing 2,3-dihydroquinazolinone compounds as nav1.8 inhibitors | |
| JP6758374B2 (ja) | Ｉｄｈ２突然変異を標的とする抗腫瘍化合物及びその使用方法 |