JP6094578B2 - 代謝性障害の治療のためのgpr119モジュレーターとしての置換ピペリジン - Google Patents
代謝性障害の治療のためのgpr119モジュレーターとしての置換ピペリジン Download PDFInfo
- Publication number
- JP6094578B2 JP6094578B2 JP2014514056A JP2014514056A JP6094578B2 JP 6094578 B2 JP6094578 B2 JP 6094578B2 JP 2014514056 A JP2014514056 A JP 2014514056A JP 2014514056 A JP2014514056 A JP 2014514056A JP 6094578 B2 JP6094578 B2 JP 6094578B2
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- JP
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- alkyl
- substituted
- phenyl
- cyclopropyl
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- 0 CNCCC1=*C(I)=*1 Chemical compound CNCCC1=*C(I)=*1 0.000 description 23
- MSAXWXFCWGHFFL-UHFFFAOYSA-N CC(C)c1n[o]c(N(CC2)CCC2NC2CC2)n1 Chemical compound CC(C)c1n[o]c(N(CC2)CCC2NC2CC2)n1 MSAXWXFCWGHFFL-UHFFFAOYSA-N 0.000 description 2
- LNJMHEJAYSYZKK-UHFFFAOYSA-N Cc1ncccn1 Chemical compound Cc1ncccn1 LNJMHEJAYSYZKK-UHFFFAOYSA-N 0.000 description 2
- RGTBLCLLSZPOKR-UHFFFAOYSA-N Cc1ncn[o]1 Chemical compound Cc1ncn[o]1 RGTBLCLLSZPOKR-UHFFFAOYSA-N 0.000 description 2
- QNKSWMYLUSPYAZ-AAPHRLRXSA-N C/C(/N(c(cc1)ncc1C(N(C1CC1)C(CCN(C1)c2ccc(C(F)(F)F)cn2)C1F)=O)N)=N/N Chemical compound C/C(/N(c(cc1)ncc1C(N(C1CC1)C(CCN(C1)c2ccc(C(F)(F)F)cn2)C1F)=O)N)=N/N QNKSWMYLUSPYAZ-AAPHRLRXSA-N 0.000 description 1
- OYCDNJIQKNTDFR-UHFFFAOYSA-N C=Cc1ncccc1F Chemical compound C=Cc1ncccc1F OYCDNJIQKNTDFR-UHFFFAOYSA-N 0.000 description 1
- KEKUKSKHQBPTSR-UHFFFAOYSA-N CC(C)c1n[o]c(N(CC2)CCC2=O)n1 Chemical compound CC(C)c1n[o]c(N(CC2)CCC2=O)n1 KEKUKSKHQBPTSR-UHFFFAOYSA-N 0.000 description 1
- HTUYWKYIIKVIDH-UHFFFAOYSA-N CCC(CC)=C/N=C(\N)/N(CC1)CCC1N(C1CC1)C(c(nc1)cnc1-[n]1ncnc1)=O Chemical compound CCC(CC)=C/N=C(\N)/N(CC1)CCC1N(C1CC1)C(c(nc1)cnc1-[n]1ncnc1)=O HTUYWKYIIKVIDH-UHFFFAOYSA-N 0.000 description 1
- CEAUPHHUNPGPRD-UHFFFAOYSA-N CCOc(cc1)ncc1-c(nc1)ncc1C(N(C1CC1)C1CCNCC1)=O Chemical compound CCOc(cc1)ncc1-c(nc1)ncc1C(N(C1CC1)C1CCNCC1)=O CEAUPHHUNPGPRD-UHFFFAOYSA-N 0.000 description 1
- KLCSEFGJARHHPI-UHFFFAOYSA-N CCc1cnc(N(CC2)CCC2=O)nc1 Chemical compound CCc1cnc(N(CC2)CCC2=O)nc1 KLCSEFGJARHHPI-UHFFFAOYSA-N 0.000 description 1
- PCBRKNRKGSLBES-UHFFFAOYSA-N CCc1cnc(N(CC2)CCC2N(C2CC2)C(c2ccc(-[n]3cncc3)nn2)=O)nc1 Chemical compound CCc1cnc(N(CC2)CCC2N(C2CC2)C(c2ccc(-[n]3cncc3)nn2)=O)nc1 PCBRKNRKGSLBES-UHFFFAOYSA-N 0.000 description 1
- FEZOYGSDMSGLKF-UHFFFAOYSA-N CCc1cnc(N(CC2)CCC2N(C2CC2)C(c2cnc(-[n]3c(C)ncc3)nc2)=O)nc1 Chemical compound CCc1cnc(N(CC2)CCC2N(C2CC2)C(c2cnc(-[n]3c(C)ncc3)nc2)=O)nc1 FEZOYGSDMSGLKF-UHFFFAOYSA-N 0.000 description 1
- ZXENSRNGQLLLQP-RBUKOAKNSA-N CCc1cnc(N(CC[C@H]2N(C3CC3)C(c(cc3)cnc3-[n]3nnnc3C)=O)C[C@@H]2F)nc1 Chemical compound CCc1cnc(N(CC[C@H]2N(C3CC3)C(c(cc3)cnc3-[n]3nnnc3C)=O)C[C@@H]2F)nc1 ZXENSRNGQLLLQP-RBUKOAKNSA-N 0.000 description 1
- CZQSEYWYGNEWBZ-RMSVRTADSA-N CCc1cnc(N(CC[C@H]2N(C3CC3)C(c(cc3)cnc3N3N=C[N-]C3C)=O)C[C@@H]2F)nc1 Chemical compound CCc1cnc(N(CC[C@H]2N(C3CC3)C(c(cc3)cnc3N3N=C[N-]C3C)=O)C[C@@H]2F)nc1 CZQSEYWYGNEWBZ-RMSVRTADSA-N 0.000 description 1
- MIVYGBNHFGFZNE-FUHWJXTLSA-N CCc1cnc(N(CC[C@H]2N(C3CC3)C(c(nc3)cnc3-[n]3ncnc3)=O)C[C@@H]2F)nc1 Chemical compound CCc1cnc(N(CC[C@H]2N(C3CC3)C(c(nc3)cnc3-[n]3ncnc3)=O)C[C@@H]2F)nc1 MIVYGBNHFGFZNE-FUHWJXTLSA-N 0.000 description 1
- BJWDVPYQXJCEQC-VQTJNVASSA-N CCc1cnc(N(CC[C@H]2N(C3CC3)C(c3cnc(-[n]4c(C)ncc4)nc3)=O)C[C@@H]2F)nc1 Chemical compound CCc1cnc(N(CC[C@H]2N(C3CC3)C(c3cnc(-[n]4c(C)ncc4)nc3)=O)C[C@@H]2F)nc1 BJWDVPYQXJCEQC-VQTJNVASSA-N 0.000 description 1
- NZYOGBPIJUCENG-UHFFFAOYSA-N COC(C1)(C(OC)=O)ON=C1c(ccc(C#N)c1)c1F Chemical compound COC(C1)(C(OC)=O)ON=C1c(ccc(C#N)c1)c1F NZYOGBPIJUCENG-UHFFFAOYSA-N 0.000 description 1
- ZQWUUPBHODOKMW-UHFFFAOYSA-N CS(c(cc1)ccc1-c(cc1)ncc1C(N(C1CC1)C(CC1)CCN1C#N)=O)(=O)=O Chemical compound CS(c(cc1)ccc1-c(cc1)ncc1C(N(C1CC1)C(CC1)CCN1C#N)=O)(=O)=O ZQWUUPBHODOKMW-UHFFFAOYSA-N 0.000 description 1
- RCHXPUNNONXPFJ-UHFFFAOYSA-N CS(c(cc1)ccc1-c(nc1)ncc1C(N(C1CC1)C1CCNCC1)=O)(=O)=O Chemical compound CS(c(cc1)ccc1-c(nc1)ncc1C(N(C1CC1)C1CCNCC1)=O)(=O)=O RCHXPUNNONXPFJ-UHFFFAOYSA-N 0.000 description 1
- PSOZJOZKEVZLKZ-UHFFFAOYSA-N Cc1c[o]c(C)n1 Chemical compound Cc1c[o]c(C)n1 PSOZJOZKEVZLKZ-UHFFFAOYSA-N 0.000 description 1
- LCZUOKDVTBMCMX-UHFFFAOYSA-N Cc1cnc(C)cn1 Chemical compound Cc1cnc(C)cn1 LCZUOKDVTBMCMX-UHFFFAOYSA-N 0.000 description 1
- CYGOSSQUEMVYHG-UHFFFAOYSA-N Cc1cnc(N(CC2)CCC2NC2CC2)nc1 Chemical compound Cc1cnc(N(CC2)CCC2NC2CC2)nc1 CYGOSSQUEMVYHG-UHFFFAOYSA-N 0.000 description 1
- FICAQKBMCKEFDI-UHFFFAOYSA-N Cc1n[o]c(C)c1 Chemical compound Cc1n[o]c(C)c1 FICAQKBMCKEFDI-UHFFFAOYSA-N 0.000 description 1
- FZAXBPZVVJOFKX-UHFFFAOYSA-N Cc1n[o]cn1 Chemical compound Cc1n[o]cn1 FZAXBPZVVJOFKX-UHFFFAOYSA-N 0.000 description 1
- MLPCMXYDRKUMGD-UHFFFAOYSA-N Cc1ncc[n]1-c(nc1)ncc1C(N(C1CC1)C(CCN(C1)c2ccc(C(F)(F)F)cn2)C1F)=O Chemical compound Cc1ncc[n]1-c(nc1)ncc1C(N(C1CC1)C(CCN(C1)c2ccc(C(F)(F)F)cn2)C1F)=O MLPCMXYDRKUMGD-UHFFFAOYSA-N 0.000 description 1
- IDQXGDSGPZNQTN-PKOBYXMFSA-N Cc1ncc[n]1-c1ncc(C(N(C2CC2)[C@H](CCN(C2)c3ccc(C(F)(F)F)cn3)[C@H]2F)=O)nc1 Chemical compound Cc1ncc[n]1-c1ncc(C(N(C2CC2)[C@H](CCN(C2)c3ccc(C(F)(F)F)cn3)[C@H]2F)=O)nc1 IDQXGDSGPZNQTN-PKOBYXMFSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N Cc1ncccc1 Chemical compound Cc1ncccc1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- CAWHJQAVHZEVTJ-UHFFFAOYSA-N Cc1nccnc1 Chemical compound Cc1nccnc1 CAWHJQAVHZEVTJ-UHFFFAOYSA-N 0.000 description 1
- DRSCBBSCLOQJIA-UHFFFAOYSA-N FC(c1cc(F)c(N(CC2)CCC2NC2CC2)nc1)(F)F Chemical compound FC(c1cc(F)c(N(CC2)CCC2NC2CC2)nc1)(F)F DRSCBBSCLOQJIA-UHFFFAOYSA-N 0.000 description 1
- BGZZTHSVOJZJEG-UHFFFAOYSA-N O=C(c(nc1)cnc1-[n]1ncnc1)N(C1CC1)C(CCN(C1)c2ccc(C(F)(F)F)cn2)C1F Chemical compound O=C(c(nc1)cnc1-[n]1ncnc1)N(C1CC1)C(CCN(C1)c2ccc(C(F)(F)F)cn2)C1F BGZZTHSVOJZJEG-UHFFFAOYSA-N 0.000 description 1
- LIVDOBRCIKCBIC-UHFFFAOYSA-N O=C(c1cnc(-[n]2cncc2)nc1)N(C1CC1)C(CC1)CCN1c1nc(-c2ccccc2)n[o]1 Chemical compound O=C(c1cnc(-[n]2cncc2)nc1)N(C1CC1)C(CC1)CCN1c1nc(-c2ccccc2)n[o]1 LIVDOBRCIKCBIC-UHFFFAOYSA-N 0.000 description 1
- DBVGKAMVRRIHQQ-UHFFFAOYSA-N O=C(c1cnc(-c2ccncc2)nc1)N(C1CC1)C(CC1)CCN1c1nc(-c2ccccc2)n[o]1 Chemical compound O=C(c1cnc(-c2ccncc2)nc1)N(C1CC1)C(CC1)CCN1c1nc(-c2ccccc2)n[o]1 DBVGKAMVRRIHQQ-UHFFFAOYSA-N 0.000 description 1
- ZFPKPRDCQBIPAY-UHFFFAOYSA-O [NH2+]=C(N(CC1)CCC1N(C1CC1)C(c1cnc(-[n]2cncc2)nc1)=O)/N=C(/C1CC1)\O Chemical compound [NH2+]=C(N(CC1)CCC1N(C1CC1)C(c1cnc(-[n]2cncc2)nc1)=O)/N=C(/C1CC1)\O ZFPKPRDCQBIPAY-UHFFFAOYSA-O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11169297.6 | 2011-06-09 | ||
| EP11169297 | 2011-06-09 | ||
| PCT/EP2012/060729 WO2012168315A1 (en) | 2011-06-09 | 2012-06-06 | Substituted piperidines as gpr119 modulators for the treatment of metabolic disorders |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014516070A JP2014516070A (ja) | 2014-07-07 |
| JP2014516070A5 JP2014516070A5 (https=) | 2015-07-23 |
| JP6094578B2 true JP6094578B2 (ja) | 2017-03-15 |
Family
ID=46245574
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014514056A Active JP6094578B2 (ja) | 2011-06-09 | 2012-06-06 | 代謝性障害の治療のためのgpr119モジュレーターとしての置換ピペリジン |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8921398B2 (https=) |
| EP (1) | EP2718288B1 (https=) |
| JP (1) | JP6094578B2 (https=) |
| AR (1) | AR086895A1 (https=) |
| WO (1) | WO2012168315A1 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8822471B2 (en) | 2011-03-14 | 2014-09-02 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| US8921398B2 (en) | 2011-06-09 | 2014-12-30 | Boehringer Ingelheim International Gmbh | N-cyclopropyl-N-piperidinyl-amide derivatives, pharmaceutical compositions and uses thereof |
| CA2878625A1 (en) | 2012-07-11 | 2014-01-16 | Elcelyx Therapeutics, Inc. | Compositions comprising statins, biguanides and further agents for reducing cardiometabolic risk |
| WO2014019967A1 (en) * | 2012-08-02 | 2014-02-06 | Boehringer Ingelheim International Gmbh | N-cyclopropyl-n-piperidinyl-amides, pharmaceutical compositions containing them and uses thereof |
| WO2014048882A1 (de) * | 2012-09-25 | 2014-04-03 | Bayer Cropscience Ag | Herbizid und fungizid wirksame 5-oxy-substituierte 3-phenylisoxazolin-5-carboxamide und 5-oxy-substituierte 3-phenylisoxazolin-5-thioamide |
| HRP20230313T1 (hr) | 2016-07-28 | 2023-05-12 | Idorsia Pharmaceuticals Ltd | Modulatori receptora cxcr7 piperidina |
| KR102502046B1 (ko) | 2018-01-26 | 2023-02-20 | 이도르시아 파마슈티컬스 리미티드 | Cxcr7 수용체 작동제 (3s,4s)-1-시클로프로필메틸-4-{[5-(2,4-디플루오로-페닐)-이속사졸-3-카르보닐]-아미노}-피페리딘-3-카르복실산 (1-피리미딘-2-일-시클로프로필)-아미드의 결정질 형태 |
| KR20210123337A (ko) * | 2019-01-31 | 2021-10-13 | 더 내셔널 인스티튜츠 오브 파마슈티컬 알앤디 컴퍼니 리미티드 | 방향족 고리 또는 헤테로방향족 고리 화합물, 이의 제조 방법 및 이의 의학 용도 |
| WO2025128834A1 (en) * | 2023-12-15 | 2025-06-19 | Alterome Therapeutics, Inc. | Akt1 modulators |
| WO2025207620A1 (en) * | 2024-03-27 | 2025-10-02 | Alterome Therapeutics, Inc. | Akt1 modulators |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI326214B (en) | 2002-07-17 | 2010-06-21 | Avanir Pharmaceuticals Inc | Pharmaceutical compositions comprising dextromethorphan and quinidine for the treatment of neurological disorders |
| WO2004041282A1 (ja) | 2002-11-06 | 2004-05-21 | Takeda Pharmaceutical Company Limited | 受容体調節剤 |
| US20070032475A1 (en) | 2005-04-15 | 2007-02-08 | Ye Xiaocong M | Novel compounds useful for bradykinin B1 receptor antagonism |
| EP1928236B1 (en) * | 2005-09-27 | 2011-11-23 | Irm Llc | Diarylamine-containing compounds and compositions, and their use as modulators of c-kit receptors |
| US8039458B2 (en) | 2005-11-17 | 2011-10-18 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| US7659287B2 (en) * | 2006-06-08 | 2010-02-09 | Amgen Inc. | Benzamide derivatives and uses related thereto |
| US20080103123A1 (en) | 2006-08-30 | 2008-05-01 | Biovitrum | New compounds |
| EP2134704B1 (en) | 2007-03-08 | 2010-09-22 | Irm Llc | Compounds and compositions as modulators of gpr119 activity |
| GB0812649D0 (en) | 2008-07-10 | 2008-08-20 | Prosidion Ltd | Compounds |
| GB0812648D0 (en) | 2008-07-10 | 2008-08-20 | Prosidion Ltd | Compounds |
| JP5657566B2 (ja) * | 2008-12-24 | 2015-01-21 | バイアル ポルテラ アンド シーエイ エス エイBIAL−Portela & Ca, S.A. | 医薬品 |
| US8481731B2 (en) | 2009-06-24 | 2013-07-09 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical composition and methods relating thereto |
| EA201200046A1 (ru) | 2009-06-24 | 2012-08-30 | Бёрингер Ингельхайм Интернациональ Гмбх | Новые соединения, фармацевтическая композиция и связанные с ними способы |
| EP2566864B1 (en) | 2010-05-07 | 2014-09-03 | Boehringer Ingelheim International GmbH | Pyridazinones as gpr119 agonists |
| UY33805A (es) | 2010-12-17 | 2012-07-31 | Boehringer Ingelheim Int | ?Derivados de dihidrobenzofuranil-piperidinilo, aza-dihidrobenzofuranilpiperidinilo y diaza-dihidrobenzofuranil-piperidinilo, composiciones farmacéuticas que los contienen y usos de los mismos?. |
| US8778926B2 (en) | 2011-01-21 | 2014-07-15 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| US8822471B2 (en) | 2011-03-14 | 2014-09-02 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| US8921398B2 (en) | 2011-06-09 | 2014-12-30 | Boehringer Ingelheim International Gmbh | N-cyclopropyl-N-piperidinyl-amide derivatives, pharmaceutical compositions and uses thereof |
-
2012
- 2012-06-06 US US13/489,557 patent/US8921398B2/en active Active
- 2012-06-06 EP EP12726611.2A patent/EP2718288B1/en active Active
- 2012-06-06 WO PCT/EP2012/060729 patent/WO2012168315A1/en not_active Ceased
- 2012-06-06 JP JP2014514056A patent/JP6094578B2/ja active Active
- 2012-06-08 AR ARP120102062A patent/AR086895A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2014516070A (ja) | 2014-07-07 |
| AR086895A1 (es) | 2014-01-29 |
| WO2012168315A1 (en) | 2012-12-13 |
| EP2718288A1 (en) | 2014-04-16 |
| EP2718288B1 (en) | 2015-03-11 |
| US20130143892A1 (en) | 2013-06-06 |
| US8921398B2 (en) | 2014-12-30 |
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