JP6479763B2 - 第xia因子阻害剤としての置換アゾール含有のテトラヒドロイソキノリン - Google Patents
第xia因子阻害剤としての置換アゾール含有のテトラヒドロイソキノリン Download PDFInfo
- Publication number
- JP6479763B2 JP6479763B2 JP2016505527A JP2016505527A JP6479763B2 JP 6479763 B2 JP6479763 B2 JP 6479763B2 JP 2016505527 A JP2016505527 A JP 2016505527A JP 2016505527 A JP2016505527 A JP 2016505527A JP 6479763 B2 JP6479763 B2 JP 6479763B2
- Authority
- JP
- Japan
- Prior art keywords
- carbonyl
- tetrahydroisoquinoline
- chloro
- fluorophenyl
- benzoic acid
- 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.)
- Expired - Fee Related
Links
- 0 CN(CC1)C(C(N*(I)=C)=O)c2c1c(*I)ccc2 Chemical compound CN(CC1)C(C(N*(I)=C)=O)c2c1c(*I)ccc2 0.000 description 11
- VOFBKPLGCKRATB-UHFFFAOYSA-N CC(C1)(C(O)=O)ON=C1c(cccc1Cl)c1F Chemical compound CC(C1)(C(O)=O)ON=C1c(cccc1Cl)c1F VOFBKPLGCKRATB-UHFFFAOYSA-N 0.000 description 1
- LEGCVLXVQJXNEL-UHFFFAOYSA-N CC1(COc2cccc(C3C(Nc(cc4)ccc4C(O)=O)=O)c2CCN3C(c2c[n](-c(cccc3Cl)c3F)nn2)=O)COC1 Chemical compound CC1(COc2cccc(C3C(Nc(cc4)ccc4C(O)=O)=O)c2CCN3C(c2c[n](-c(cccc3Cl)c3F)nn2)=O)COC1 LEGCVLXVQJXNEL-UHFFFAOYSA-N 0.000 description 1
- DJUCOOVKTPLJLE-UHFFFAOYSA-N CN(C)C(CC1)CCN1c1cccc(C2C(Nc(cc3)ccc3-c3ncc[o]3)=O)c1CCN2C(c1c[n](-c2cccc(Cl)c2F)nc1)=O Chemical compound CN(C)C(CC1)CCN1c1cccc(C2C(Nc(cc3)ccc3-c3ncc[o]3)=O)c1CCN2C(c1c[n](-c2cccc(Cl)c2F)nc1)=O DJUCOOVKTPLJLE-UHFFFAOYSA-N 0.000 description 1
- RZCBNXHMENKKFK-PQHLKRTFSA-N CNC(c(nc1)ccc1-c1c(CCN([C@H]2C(Nc(cc3)ccc3C(O)=O)=O)C([C@@H](C3)ON=C3c(cccc3Cl)c3F)=O)c2ccc1)=O Chemical compound CNC(c(nc1)ccc1-c1c(CCN([C@H]2C(Nc(cc3)ccc3C(O)=O)=O)C([C@@H](C3)ON=C3c(cccc3Cl)c3F)=O)c2ccc1)=O RZCBNXHMENKKFK-PQHLKRTFSA-N 0.000 description 1
- PTJPEVRPDJCNBG-MRIBFJTASA-N Cc(c(N/C=C(/C(O)[O]=C)\C=N)ccc1)c1Cl Chemical compound Cc(c(N/C=C(/C(O)[O]=C)\C=N)ccc1)c1Cl PTJPEVRPDJCNBG-MRIBFJTASA-N 0.000 description 1
- LNKXXEMOPNVZGM-UHFFFAOYSA-N Cc1n[n](C)c(CC2)c1C(C(Nc(cc1)ccc1C(O)=O)=O)N2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O Chemical compound Cc1n[n](C)c(CC2)c1C(C(Nc(cc1)ccc1C(O)=O)=O)N2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O LNKXXEMOPNVZGM-UHFFFAOYSA-N 0.000 description 1
- NGVXSPZNILPQBM-UHFFFAOYSA-N NC(c(cc1)ccc1NC(C(c1c(CC2)c(N(CC3)CCC3N(CCC3)C3=O)ccc1)N2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O)=O)=O Chemical compound NC(c(cc1)ccc1NC(C(c1c(CC2)c(N(CC3)CCC3N(CCC3)C3=O)ccc1)N2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O)=O)=O NGVXSPZNILPQBM-UHFFFAOYSA-N 0.000 description 1
- YTULCQGNUIGFGU-UHFFFAOYSA-N NCc1cccc(C2C(Nc(cc3)ccc3C(O)=O)=O)c1CCN2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O Chemical compound NCc1cccc(C2C(Nc(cc3)ccc3C(O)=O)=O)c1CCN2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O YTULCQGNUIGFGU-UHFFFAOYSA-N 0.000 description 1
- AKPYALCPZPVVAN-UHFFFAOYSA-N OC(C(C1)ON=C1c(c(F)c(cc1)Cl)c1F)=O Chemical compound OC(C(C1)ON=C1c(c(F)c(cc1)Cl)c1F)=O AKPYALCPZPVVAN-UHFFFAOYSA-N 0.000 description 1
- DTPSCOKGXYBDJF-UHFFFAOYSA-N OC(C(CC1=O)CN1c1cccc(Cl)c1F)=O Chemical compound OC(C(CC1=O)CN1c1cccc(Cl)c1F)=O DTPSCOKGXYBDJF-UHFFFAOYSA-N 0.000 description 1
- OHZPVCRHBZYZJT-UHFFFAOYSA-N OC(c(cc1)ccc1NC(C(c1c(CC2)c(N(CC3)CCC3N(CCC3)C3=O)ccc1)N2C(c(nc1)c[n]1-c(cccc1Cl)c1F)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC(C(c1c(CC2)c(N(CC3)CCC3N(CCC3)C3=O)ccc1)N2C(c(nc1)c[n]1-c(cccc1Cl)c1F)=O)=O)=O OHZPVCRHBZYZJT-UHFFFAOYSA-N 0.000 description 1
- AMHCONOGPXXSHI-UHFFFAOYSA-N OC(c(cc1)ccc1NC(C(c1c(CC2)c(OC3COC3)ccc1)N2C(c1c[n](-c2cccc(Cl)c2F)nn1)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC(C(c1c(CC2)c(OC3COC3)ccc1)N2C(c1c[n](-c2cccc(Cl)c2F)nn1)=O)=O)=O AMHCONOGPXXSHI-UHFFFAOYSA-N 0.000 description 1
- OFIYZOXNLSDWIA-XRKRLSELSA-N OC(c(cc1)ccc1NC([C@@H](c1c(CC2)c(N3CCN(CC(F)(F)F)CC3)ccc1)N2C([C@@H](C1)ON=C1c(cccc1Cl)c1F)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@@H](c1c(CC2)c(N3CCN(CC(F)(F)F)CC3)ccc1)N2C([C@@H](C1)ON=C1c(cccc1Cl)c1F)=O)=O)=O OFIYZOXNLSDWIA-XRKRLSELSA-N 0.000 description 1
- HRLKIYSEPAYSAH-HSZRJFAPSA-N OC(c(cc1)ccc1NC([C@@H](c1ccccc1CC1)N1C(c1c[n](-c(cccc2Cl)c2F)nn1)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@@H](c1ccccc1CC1)N1C(c1c[n](-c(cccc2Cl)c2F)nn1)=O)=O)=O HRLKIYSEPAYSAH-HSZRJFAPSA-N 0.000 description 1
- QWULNBLKJBJATC-BHYZAODMSA-N OC(c(cc1)ccc1NC([C@H](c1c(CC2)c(N(CC3)CCC3C3COC3)ccc1)N2C([C@@H](C1)ON=C1c(cccc1Cl)c1F)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@H](c1c(CC2)c(N(CC3)CCC3C3COC3)ccc1)N2C([C@@H](C1)ON=C1c(cccc1Cl)c1F)=O)=O)=O QWULNBLKJBJATC-BHYZAODMSA-N 0.000 description 1
- UCSKYPRDSCVAMS-MHZLTWQESA-N OC(c(cc1)ccc1NC([C@H](c1c(CC2)c(N3CCOCC3)ccc1)N2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@H](c1c(CC2)c(N3CCOCC3)ccc1)N2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O)=O)=O UCSKYPRDSCVAMS-MHZLTWQESA-N 0.000 description 1
- JQEHHXASFNDRCX-UHFFFAOYSA-N OC(c1c[o]c(-c(cccc2Cl)c2F)n1)=O Chemical compound OC(c1c[o]c(-c(cccc2Cl)c2F)n1)=O JQEHHXASFNDRCX-UHFFFAOYSA-N 0.000 description 1
- NYQZRXFSTDWBHC-UHFFFAOYSA-N OCCNc1cccc(C2C(Nc(cc3)ccc3C(O)=O)=O)c1CCN2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O Chemical compound OCCNc1cccc(C2C(Nc(cc3)ccc3C(O)=O)=O)c1CCN2C(c1c[n](-c(cccc2Cl)c2F)nn1)=O NYQZRXFSTDWBHC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361804883P | 2013-03-25 | 2013-03-25 | |
| US61/804,883 | 2013-03-25 | ||
| US201361840736P | 2013-06-28 | 2013-06-28 | |
| US61/840,736 | 2013-06-28 | ||
| US201361894607P | 2013-10-23 | 2013-10-23 | |
| US61/894,607 | 2013-10-23 | ||
| PCT/US2014/031651 WO2014160668A1 (en) | 2013-03-25 | 2014-03-25 | Tetrahydroisoquinolines containing substituted azoles as factor xia inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016519096A JP2016519096A (ja) | 2016-06-30 |
| JP2016519096A5 JP2016519096A5 (enExample) | 2017-04-13 |
| JP6479763B2 true JP6479763B2 (ja) | 2019-03-06 |
Family
ID=50487219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016505527A Expired - Fee Related JP6479763B2 (ja) | 2013-03-25 | 2014-03-25 | 第xia因子阻害剤としての置換アゾール含有のテトラヒドロイソキノリン |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9738655B2 (enExample) |
| EP (1) | EP2978751B1 (enExample) |
| JP (1) | JP6479763B2 (enExample) |
| CN (1) | CN105228996B (enExample) |
| ES (1) | ES2712699T3 (enExample) |
| WO (1) | WO2014160668A1 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LT2766346T (lt) | 2011-10-14 | 2017-06-12 | Bristol-Myers Squibb Company | Pakeistieji tetrahidroizochinolino junginiai, kaip faktoriaus xia inhibitoriai |
| EP2906552B1 (en) | 2012-10-12 | 2017-11-22 | Bristol-Myers Squibb Company | Guanidine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
| HRP20180465T1 (hr) | 2012-10-12 | 2018-05-04 | Bristol-Myers Squibb Company | Kristalni oblici inhibitora faktora xia |
| US9403774B2 (en) | 2012-10-12 | 2016-08-02 | Bristol-Myers Squibb Company | Guanidine and amine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
| GB201314286D0 (en) | 2013-08-08 | 2013-09-25 | Takeda Pharmaceutical | Therapeutic Compounds |
| NO2760821T3 (enExample) | 2014-01-31 | 2018-03-10 | ||
| JP6505727B2 (ja) | 2014-01-31 | 2019-04-24 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | ヘテロ環式p2’基を有する第xia因子阻害剤としてのマクロ環 |
| JP6526796B2 (ja) | 2014-09-04 | 2019-06-05 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Fxia阻害剤であるジアミドマクロ環 |
| US9453018B2 (en) | 2014-10-01 | 2016-09-27 | Bristol-Myers Squibb Company | Pyrimidinones as factor XIa inhibitors |
| EP3271334A1 (de) * | 2015-03-18 | 2018-01-24 | Bayer Pharma Aktiengesellschaft | Substituierte n-bicyclo-2-arylchinolin-4-carboxamide und ihre verwendung |
| CN105541716B (zh) * | 2015-03-26 | 2024-02-23 | Agc株式会社 | 吡唑衍生物的制造方法 |
| US10160750B2 (en) | 2015-06-19 | 2018-12-25 | Bristol-Myers Squibb Company | Diamide macrocycles as factor XIa inhibitors |
| CN107849026B (zh) | 2015-07-29 | 2021-01-01 | 百时美施贵宝公司 | 携带烷基或环烷基p2′部分的因子xia大环抑制剂 |
| ES2871111T3 (es) | 2015-07-29 | 2021-10-28 | Bristol Myers Squibb Co | Inhibidores macrocíclicos del factor XIa que contienen un grupo P2' no aromático |
| WO2017074833A1 (en) | 2015-10-29 | 2017-05-04 | Merck Sharp & Dohme Corp. | Macrocyclic spirocarbamate derivatives as factor xia inhibitors, pharmaceutically acceptable compositions and their use |
| CN107540659A (zh) * | 2016-06-29 | 2018-01-05 | 四川科伦博泰生物医药股份有限公司 | 四氢异喹啉类化合物、其制备方法、药物组合物及其用途 |
| US10143681B2 (en) | 2016-08-22 | 2018-12-04 | Merck Sharp & Dohme Corp. | Factor XIa inhibitors |
| WO2018093716A1 (en) * | 2016-11-18 | 2018-05-24 | Merck Sharp & Dohme Corp. | FACTOR XIIa INHIBITORS |
| CN109867660A (zh) * | 2017-12-01 | 2019-06-11 | 四川科伦博泰生物医药股份有限公司 | 含季铵离子的四氢异喹啉酰胺化合物及其药物用途 |
| EP3778597B1 (en) * | 2018-03-28 | 2025-05-28 | Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. | Tetrahydroisoquinoline derivative, preparation method therefor and uses thereof |
| WO2019218899A1 (zh) * | 2018-05-17 | 2019-11-21 | 四川科伦博泰生物医药股份有限公司 | 含聚乙二醇醚的四氢异喹啉酰胺化合物及其药物用途 |
| US11518766B2 (en) | 2019-06-28 | 2022-12-06 | Shanghai Jemincare Pharmaceuticals Co., Ltd. | Tricyclic compound, preparation method therefor and use thereof |
| WO2021121396A1 (zh) * | 2019-12-20 | 2021-06-24 | 成都康弘药业集团股份有限公司 | 作为血浆激肽释放酶抑制剂的三环类化合物及其用途 |
| WO2021136390A1 (zh) * | 2019-12-31 | 2021-07-08 | 上海京新生物医药有限公司 | 凝血因子XIa抑制剂 |
| JP7787890B2 (ja) * | 2020-11-19 | 2025-12-17 | メルク・シャープ・アンド・ドーム・エルエルシー | 血漿カリクレイン阻害剤 |
| CN116685308A (zh) * | 2020-12-18 | 2023-09-01 | Ucb生物制药有限责任公司 | 无定形固体分散体 |
| CN117285463A (zh) * | 2023-09-04 | 2023-12-26 | 南通敏言生物医药科技有限公司 | 一种5-氨基-8-溴-2-叔丁氧羰基-1,2,3,4-四氢异喹啉的合成方法 |
Family Cites Families (103)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1525186A (fr) | 1967-03-29 | 1968-05-17 | Roussel Uclaf | Nouvelles pénicillines et procédé de préparation |
| EP0028489B1 (en) | 1979-11-05 | 1983-10-05 | Beecham Group Plc | Enzyme derivatives, and their preparation |
| DE4034829A1 (de) | 1990-11-02 | 1992-05-07 | Merck Patent Gmbh | Cyclopeptide |
| JP3190431B2 (ja) | 1991-07-01 | 2001-07-23 | 三菱化学株式会社 | ケトン誘導体 |
| GB9206757D0 (en) | 1992-03-27 | 1992-05-13 | Ferring Bv | Novel peptide receptor ligands |
| US5624936A (en) | 1995-03-29 | 1997-04-29 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| WO1996034010A2 (en) | 1995-03-29 | 1996-10-31 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| AU717298B2 (en) | 1996-04-03 | 2000-03-23 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| US5869682A (en) | 1996-04-03 | 1999-02-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| PE121699A1 (es) | 1997-02-18 | 1999-12-08 | Boehringer Ingelheim Pharma | Heterociclos biciclicos disustituidos como inhibidores de la trombina |
| ZA985247B (en) | 1997-06-19 | 1999-12-17 | Du Pont Merck Pharma | Guanidine mimics as factor Xa inhibitors. |
| TW557297B (en) | 1997-09-26 | 2003-10-11 | Abbott Lab | Rapamycin analogs having immunomodulatory activity, and pharmaceutical compositions containing same |
| PL204619B1 (pl) | 1998-03-19 | 2010-01-29 | Vertex Pharma | Pochodna peptydowa, kompozycja farmaceutyczna zawierająca taką pochodną i zastosowanie pochodnej peptydowej |
| DE69939168D1 (de) | 1998-05-26 | 2008-09-04 | Warner Lambert Co | Bicyclische pyrimidine und bicyclische 3,4-dihydropyrimidine als inhibitoren der zellvermehrung |
| US6307049B1 (en) | 1998-09-30 | 2001-10-23 | The Procter & Gamble Co. | Heterocyclic 2-substituted ketoamides |
| CA2358578A1 (en) | 1999-01-02 | 2000-07-13 | Aventis Pharma Deutschland Gmbh | Novel malonic acid derivatives, processes for their preparation, their use and pharmaceutical compositions containing them (inhibition of factor xa activity) |
| EP1016663A1 (en) | 1999-01-02 | 2000-07-05 | Aventis Pharma Deutschland GmbH | Novel malonic acid derivatives, processes for their preparation, their use and pharmaceutical compositions containing them (inhibition of factor Xa activity) |
| CA2369378A1 (en) | 1999-04-09 | 2000-10-19 | Basf Aktiengesellschaft | Low-molecular inhibitors of complement proteases |
| CA2383008A1 (en) | 1999-06-14 | 2000-12-21 | Amanda Jane Lyons | Compounds |
| DE19962924A1 (de) | 1999-12-24 | 2001-07-05 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
| EP1125925A1 (en) | 2000-02-15 | 2001-08-22 | Applied Research Systems ARS Holding N.V. | Amine derivatives for the treatment of apoptosis |
| JP2004507456A (ja) * | 2000-05-11 | 2004-03-11 | ブリストル−マイヤーズ スクイブ カンパニー | 成長ホルモン分泌促進薬として有用なテトラヒドロイソキノリン類縁体 |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| AR035216A1 (es) | 2000-12-01 | 2004-05-05 | Astrazeneca Ab | Derivados de acido mandelico ,derivados farmaceuticamente aceptables, uso de estos derivados para la fabricacion de medicamentos, metodos de tratamiento ,procesos para la preparacion de estos derivados, y compuestos intermediarios |
| AU2002322802A1 (en) | 2001-07-27 | 2003-02-17 | Merck And Co., Inc. | Thrombin inhibitors |
| AU2002341693B2 (en) | 2001-09-21 | 2008-05-29 | Bristol-Myers Squibb Holdings Ireland Unlimited Company | Lactam-containing compounds and derivatives thereof as factor Xa inhibitors |
| US6649606B1 (en) * | 2001-11-09 | 2003-11-18 | Bristol-Myers Squibb Co. | Tetrahydroisoquinoline analogs as modulators of chemokine receptor activity |
| US20040180855A1 (en) | 2003-02-19 | 2004-09-16 | Schumacher William A. | Methods of treating thrombosis with reduced risk of increased bleeding times |
| US7138412B2 (en) | 2003-03-11 | 2006-11-21 | Bristol-Myers Squibb Company | Tetrahydroquinoline derivatives useful as serine protease inhibitors |
| US7129264B2 (en) | 2003-04-16 | 2006-10-31 | Bristol-Myers Squibb Company | Biarylmethyl indolines and indoles as antithromboembolic agents |
| US7544699B2 (en) * | 2003-08-08 | 2009-06-09 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds, compositions, and methods of use |
| US7417063B2 (en) | 2004-04-13 | 2008-08-26 | Bristol-Myers Squibb Company | Bicyclic heterocycles useful as serine protease inhibitors |
| US7429604B2 (en) | 2004-06-15 | 2008-09-30 | Bristol Myers Squibb Company | Six-membered heterocycles useful as serine protease inhibitors |
| US7453002B2 (en) | 2004-06-15 | 2008-11-18 | Bristol-Myers Squibb Company | Five-membered heterocycles useful as serine protease inhibitors |
| BRPI0513310A (pt) | 2004-07-12 | 2008-05-06 | Idun Pharmaceuticals Inc | análogos de tetrapeptìdeo |
| AR051596A1 (es) | 2004-10-26 | 2007-01-24 | Irm Llc | Compuestos heterociclicos condensados nitrogenados como inhibidores de la actividad del receptor canabinoide 1; composiciones farmaceuticas que los contienen y su empleo en la preparacion de medicamentos para el tratamiento de trastornos alimentarios |
| CN101137412B (zh) | 2005-01-13 | 2012-11-07 | 布里斯托尔-迈尔斯·斯奎布公司 | 用作凝血因子XIa抑制剂的取代的二芳基化合物 |
| US20060183771A1 (en) | 2005-02-17 | 2006-08-17 | Seiffert Dietmar A | Novel combination of selective factor VIIa and/or factor XIa inhibitors and selective plasma kallikrein inhibitors |
| CA2612279C (en) | 2005-06-17 | 2014-04-15 | Basf Aktiengesellschaft | Process of producing bleach boosters |
| BRPI0618523A2 (pt) * | 2005-11-11 | 2011-09-06 | Hoffmann La Roche | compostos de aminas cìclicas fundidas carbocìclicas, composições farmacêuticas e usos dos mesmos |
| AU2006325746A1 (en) | 2005-12-14 | 2007-06-21 | Bristol-Myers Squibb Company | Six-membered heterocycles useful as serine protease inhibitors |
| JP5225098B2 (ja) | 2005-12-14 | 2013-07-03 | ブリストル−マイヤーズ スクイブ カンパニー | 第XIa因子インヒビターとしてのアリールプロピオンアミド、アリールアクリルアミド、アリールプロピンアミド、またはアリールメチルウレアアナログ |
| US8466295B2 (en) | 2005-12-14 | 2013-06-18 | Bristol-Myers Squibb Company | Thiophene derivatives as factor XIa inhibitors |
| TW200745062A (en) | 2005-12-23 | 2007-12-16 | Bristol Myers Squibb Co | Macrocyclic factor VIIA inhibitors useful as anticoagulants |
| NZ575652A (en) | 2006-08-23 | 2011-08-26 | Valeant Pharmaceuticals Int | Derivatives of 4-(n-azacycloalkyl) anilides as potassium channel modulators |
| ES2546815T3 (es) | 2006-12-15 | 2015-09-28 | Bristol-Myers Squibb Company | Análogos de arilpropilamida, arilacrilamida, arilpropinamida o arilmetilurea como inhibidores del factor XIa |
| PE20081775A1 (es) | 2006-12-20 | 2008-12-18 | Bristol Myers Squibb Co | Compuestos macrociclicos como inhibidores del factor viia |
| KR20100037600A (ko) | 2007-06-13 | 2010-04-09 | 브리스톨-마이어스 스큅 컴퍼니 | 응고 인자 억제제로서의 디펩티드 유사체 |
| CN102026996B (zh) | 2008-03-13 | 2015-01-07 | 百时美施贵宝公司 | 作为凝血因子xia抑制剂的哒嗪衍生物 |
| MX2011004680A (es) | 2008-11-06 | 2011-05-25 | Astrazeneca Ab | Moduladores de beta amiloide. |
| US8507493B2 (en) | 2009-04-20 | 2013-08-13 | Abbvie Inc. | Amide and amidine derivatives and uses thereof |
| WO2010151317A1 (en) | 2009-06-22 | 2010-12-29 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| WO2011002520A2 (en) | 2009-07-02 | 2011-01-06 | Angion Biomedica Corp. | Small molecule inhibitors of parp activity |
| EP2462123B1 (en) | 2009-08-04 | 2013-10-02 | Merck Sharp & Dohme Corp. | 4,5,6-trisubstituted pyrimidine derivatives as factor ixa inhibitors |
| JP5844287B2 (ja) | 2010-02-11 | 2016-01-13 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 第xia因子阻害剤としてのマクロ環 |
| EP2729150B1 (en) | 2011-07-08 | 2016-09-14 | Merck Sharp & Dohme Corp. | Factor ixa inhibitors |
| TW201319068A (zh) | 2011-08-05 | 2013-05-16 | 必治妥美雅史谷比公司 | 作為xia因子抑制劑之環狀p1接合劑 |
| TW201311689A (zh) | 2011-08-05 | 2013-03-16 | 必治妥美雅史谷比公司 | 作為因子xia抑制劑之新穎巨環化合物 |
| LT2766346T (lt) | 2011-10-14 | 2017-06-12 | Bristol-Myers Squibb Company | Pakeistieji tetrahidroizochinolino junginiai, kaip faktoriaus xia inhibitoriai |
| IN2014CN02806A (enExample) | 2011-10-14 | 2015-07-03 | Bristol Myers Squibb Co | |
| IN2014CN02805A (enExample) * | 2011-10-14 | 2015-07-03 | Bristol Myers Squibb Co | |
| GB2497806A (en) | 2011-12-21 | 2013-06-26 | Ono Pharmaceutical Co | Pyridinone and pyrimidinone derivatives as factor XIa inhibitors |
| WO2013093484A1 (en) | 2011-12-21 | 2013-06-27 | Ono Pharmaceutical Co., Ltd. | Pyridinone and pyrimidinone derivatives as factor xia inhibitors |
| US20140378474A1 (en) | 2012-01-27 | 2014-12-25 | Novartis Ag | 5-membered heteroarylcarboxamide derivatives as plasma kallikrein inhibitors |
| US20140350034A1 (en) | 2012-01-27 | 2014-11-27 | Novartis Ag | Aminopyridine derivatives as plasma kallikrein inhibitors |
| JP2015083542A (ja) | 2012-02-08 | 2015-04-30 | 大日本住友製薬株式会社 | 3位置換プロリン誘導体 |
| US9783614B2 (en) | 2012-05-10 | 2017-10-10 | Bayer Pharma Aktiengesellschaft | Antibodies capable of binding to the coagulation Factor XI and/or its activated form factor Xia and uses thereof |
| GB201209138D0 (en) | 2012-05-24 | 2012-07-04 | Ono Pharmaceutical Co | Compounds |
| US9758480B2 (en) | 2012-07-19 | 2017-09-12 | Sumitomo Dainippon Pharma Co., Ltd. | 1-(cycloalkyl-carbonyl)proline derivative |
| CA2880898A1 (en) | 2012-08-03 | 2014-02-06 | Bristol-Myers Squibb Company | Dihydropyridone p1 as factor xia inhibitors |
| KR20150038372A (ko) | 2012-08-03 | 2015-04-08 | 브리스톨-마이어스 스큅 컴퍼니 | 인자 XIa 억제제로서의 디히드로피리돈 P1 |
| EP2906552B1 (en) | 2012-10-12 | 2017-11-22 | Bristol-Myers Squibb Company | Guanidine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
| HRP20180465T1 (hr) | 2012-10-12 | 2018-05-04 | Bristol-Myers Squibb Company | Kristalni oblici inhibitora faktora xia |
| US9403774B2 (en) | 2012-10-12 | 2016-08-02 | Bristol-Myers Squibb Company | Guanidine and amine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
| WO2014120346A1 (en) | 2012-12-19 | 2014-08-07 | Merck Sharp & Dohme Corp. | Factor ixa inhibitors |
| GB201300304D0 (en) | 2013-01-08 | 2013-02-20 | Kalvista Pharmaceuticals Ltd | Benzylamine derivatives |
| GB2510407A (en) | 2013-02-04 | 2014-08-06 | Kalvista Pharmaceuticals Ltd | Aqueous suspensions of kallikrein inhibitors for parenteral administration |
| TWI633089B (zh) | 2013-03-28 | 2018-08-21 | 拜耳製藥股份有限公司 | 經取代的酮基吡啶衍生物 |
| US9475809B2 (en) | 2013-07-23 | 2016-10-25 | Bayer Pharma Aktiengesellschaft | Substituted oxopyridine derivatives and use thereof as factor xia/plasma |
| US20160280699A1 (en) | 2013-09-26 | 2016-09-29 | Bayer Pharma Aktiengesellschaft | Substituted phenylalanine derivatives |
| EP3049408A1 (de) | 2013-09-26 | 2016-08-03 | Bayer Pharma Aktiengesellschaft | Substituierte phenylalanin-derivate |
| SG11201601963TA (en) | 2013-09-26 | 2016-04-28 | Bayer Pharma AG | Substituted phenylalanine derivatives |
| WO2015044165A1 (de) | 2013-09-26 | 2015-04-02 | Bayer Pharma Aktiengesellschaft | Substituierte phenylalanin-derivate |
| EP3049394A1 (de) | 2013-09-26 | 2016-08-03 | Bayer Pharma Aktiengesellschaft | Substituierte phenylalanin-derivate als faktor xia modulatoren |
| EP3049410A1 (de) | 2013-09-26 | 2016-08-03 | Bayer Pharma Aktiengesellschaft | Substituierte phenylalanin-derivate als faktor xia modulatoren |
| TW201605809A (zh) | 2013-09-26 | 2016-02-16 | 拜耳製藥股份有限公司 | 經取代苯丙胺酸衍生物(一) |
| EP3049406A1 (de) | 2013-09-26 | 2016-08-03 | Bayer Pharma Aktiengesellschaft | Substituierte phenylalanin-derivate und ihre verwendung zur behandlung von thrombotischen / thromboembolischen erkrankungen |
| EP3049435A4 (en) | 2013-09-27 | 2017-03-29 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
| EP3054944B1 (en) | 2013-10-07 | 2019-12-04 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
| JP6337750B2 (ja) | 2013-11-22 | 2018-06-06 | 小野薬品工業株式会社 | 化合物 |
| EP3095786A4 (en) | 2014-01-14 | 2017-10-11 | Sumitomo Dainippon Pharma Co., Ltd. | Condensed 5-oxazolidinone derivative |
| NO2760821T3 (enExample) | 2014-01-31 | 2018-03-10 | ||
| JP6505727B2 (ja) | 2014-01-31 | 2019-04-24 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | ヘテロ環式p2’基を有する第xia因子阻害剤としてのマクロ環 |
| US9499532B2 (en) | 2014-02-07 | 2016-11-22 | eXIthera Pharmaceuticals Inc. | Therapeutic compounds and compositions |
| US9663527B2 (en) | 2014-02-11 | 2017-05-30 | Merck Sharp & Dohme Corp. | Factor XIa inhibitors |
| EP3104702B1 (en) | 2014-02-11 | 2022-08-10 | Merck Sharp & Dohme LLC | Factor xia inhibitors |
| EP3104703B1 (en) | 2014-02-11 | 2020-11-18 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
| WO2015120777A1 (zh) | 2014-02-14 | 2015-08-20 | 四川海思科制药有限公司 | 一种吡啶酮或嘧啶酮衍生物、及其制备方法和应用 |
| HRP20221373T1 (hr) | 2014-03-07 | 2023-01-06 | Biocryst Pharmaceuticals, Inc. | Supstituirani pirazoli kao inhibitori kalikreina u ljudskoj plazmi |
| WO2015160634A1 (en) | 2014-04-16 | 2015-10-22 | Merck Sharp & Dohme Corp. | Factor ixa inhibitors |
| WO2015160636A1 (en) | 2014-04-16 | 2015-10-22 | Merck Sharp & Dohme Corp. | Factor ixa inhibitors |
| KR20150136294A (ko) | 2014-05-27 | 2015-12-07 | 주식회사 레고켐 바이오사이언스 | 인자 XIa 억제 활성을 가지는 신규한 화합물 |
| WO2015183709A1 (en) | 2014-05-28 | 2015-12-03 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
-
2014
- 2014-03-25 JP JP2016505527A patent/JP6479763B2/ja not_active Expired - Fee Related
- 2014-03-25 US US14/777,763 patent/US9738655B2/en active Active
- 2014-03-25 CN CN201480029926.1A patent/CN105228996B/zh not_active Expired - Fee Related
- 2014-03-25 EP EP14717649.9A patent/EP2978751B1/en not_active Not-in-force
- 2014-03-25 ES ES14717649T patent/ES2712699T3/es active Active
- 2014-03-25 WO PCT/US2014/031651 patent/WO2014160668A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| US9738655B2 (en) | 2017-08-22 |
| EP2978751A1 (en) | 2016-02-03 |
| CN105228996A (zh) | 2016-01-06 |
| JP2016519096A (ja) | 2016-06-30 |
| ES2712699T3 (es) | 2019-05-14 |
| EP2978751B1 (en) | 2018-12-05 |
| US20160145263A1 (en) | 2016-05-26 |
| WO2014160668A1 (en) | 2014-10-02 |
| CN105228996B (zh) | 2017-11-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US9738655B2 (en) | Tetrahydroisoquinolines containing substituted azoles as factor XIa inhibitors | |
| JP6082463B2 (ja) | 第xia因子阻害剤としてのジヒドロピリドンp1 | |
| CN102026996B (zh) | 作为凝血因子xia抑制剂的哒嗪衍生物 | |
| JP6033317B2 (ja) | 第xia因子阻害剤としての置換テトラヒドロイソキノリン化合物 | |
| JP6033319B2 (ja) | 第XIa因子阻害剤としての置換テトラヒドロイソキノリン化合物 | |
| US10336730B2 (en) | Substituted glycine derived FXIA inhibitors | |
| US9079929B2 (en) | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors | |
| TW202310844A (zh) | 作為因子xia抑制劑之嘧啶酮 | |
| WO2015116882A1 (en) | Macrocyclic factor xia inhibitors condensed with heterocycles | |
| JP6816103B2 (ja) | 非芳香族性P2’基を担持する新規大員環の第XIa因子阻害剤 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20160219 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20170309 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20170309 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180118 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180123 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20180423 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20180620 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180703 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20180905 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180925 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20181219 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20190108 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20190206 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6479763 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |