JP5087406B2 - 治療薬ならびにその製造方法および使用方法 - Google Patents
治療薬ならびにその製造方法および使用方法 Download PDFInfo
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- JP5087406B2 JP5087406B2 JP2007543017A JP2007543017A JP5087406B2 JP 5087406 B2 JP5087406 B2 JP 5087406B2 JP 2007543017 A JP2007543017 A JP 2007543017A JP 2007543017 A JP2007543017 A JP 2007543017A JP 5087406 B2 JP5087406 B2 JP 5087406B2
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- 0 CC1=C(*)c(c(**)c(*I)c(*)c2*)c2I1 Chemical compound CC1=C(*)c(c(**)c(*I)c(*)c2*)c2I1 0.000 description 12
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- YEYOWBLSCUEEMV-UHFFFAOYSA-N CC(C)Oc1c(CO)cccc1Cl Chemical compound CC(C)Oc1c(CO)cccc1Cl YEYOWBLSCUEEMV-UHFFFAOYSA-N 0.000 description 1
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- VBFHBTJHIOLCQE-XVNBXDOJSA-N CN(Cc(cc1)cc2c1[nH]cn2)C(/C=C/c1cc(CCC(N2)=O)c2nc1)=O Chemical compound CN(Cc(cc1)cc2c1[nH]cn2)C(/C=C/c1cc(CCC(N2)=O)c2nc1)=O VBFHBTJHIOLCQE-XVNBXDOJSA-N 0.000 description 1
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- BFGGMUCUXZTLQA-UHFFFAOYSA-N CN(Cc1c(NC2)ncc(Br)c1)C2=O Chemical compound CN(Cc1c(NC2)ncc(Br)c1)C2=O BFGGMUCUXZTLQA-UHFFFAOYSA-N 0.000 description 1
- LAFWJBSGNSNFDJ-UHFFFAOYSA-N CNCc(cc1)cc2c1[o]cc2 Chemical compound CNCc(cc1)cc2c1[o]cc2 LAFWJBSGNSNFDJ-UHFFFAOYSA-N 0.000 description 1
- DPXOSZVHVILMJI-UHFFFAOYSA-N CNCc1cccc2c1cc[nH]2 Chemical compound CNCc1cccc2c1cc[nH]2 DPXOSZVHVILMJI-UHFFFAOYSA-N 0.000 description 1
- GFTNSZIYQMJJMD-UHFFFAOYSA-N C[n](cc1)c2c1c(C=O)ccc2 Chemical compound C[n](cc1)c2c1c(C=O)ccc2 GFTNSZIYQMJJMD-UHFFFAOYSA-N 0.000 description 1
- ULQVZAKCMGIOBU-UHFFFAOYSA-N Cc1c(C=O)[nH]c2c1cccc2C(F)(F)F Chemical compound Cc1c(C=O)[nH]c2c1cccc2C(F)(F)F ULQVZAKCMGIOBU-UHFFFAOYSA-N 0.000 description 1
- VIVGMQKXNPBMAH-CMDGGOBGSA-N Cc1c(CN(C)C(/C=C/c(cc2OC3)cnc2NC3=O)=O)[n](C)c2ccccc12 Chemical compound Cc1c(CN(C)C(/C=C/c(cc2OC3)cnc2NC3=O)=O)[n](C)c2ccccc12 VIVGMQKXNPBMAH-CMDGGOBGSA-N 0.000 description 1
- YNJGEBGYFHCCFM-CMDGGOBGSA-N Cc1c(CN(C)C(/C=C/c2cc(CN(C)C(CN3)=O)c3nc2)=O)[o]c2c1cccc2 Chemical compound Cc1c(CN(C)C(/C=C/c2cc(CN(C)C(CN3)=O)c3nc2)=O)[o]c2c1cccc2 YNJGEBGYFHCCFM-CMDGGOBGSA-N 0.000 description 1
- UUUZNJSKVSCNNL-SQUSKLHYSA-N Cc1c(CN(C)C(/C=C/c2cc(CN(CCC3)[C@H]3C(N3)=O)c3nc2)=O)[o]c2c1cccc2 Chemical compound Cc1c(CN(C)C(/C=C/c2cc(CN(CCC3)[C@H]3C(N3)=O)c3nc2)=O)[o]c2c1cccc2 UUUZNJSKVSCNNL-SQUSKLHYSA-N 0.000 description 1
- RGGNGJVGHGLWFB-BQYQJAHWSA-N Cc1c(CN(C)C(/C=C/c2cc(OCC(N3)=O)c3nc2)=O)c(cccc2)c2[o]1 Chemical compound Cc1c(CN(C)C(/C=C/c2cc(OCC(N3)=O)c3nc2)=O)c(cccc2)c2[o]1 RGGNGJVGHGLWFB-BQYQJAHWSA-N 0.000 description 1
- CSIXROXGCKHAKH-BQYQJAHWSA-N Cc1c(CN(C)C(/C=C/c2cc(OCCN3)c3nc2)=O)[o]c2ccccc12 Chemical compound Cc1c(CN(C)C(/C=C/c2cc(OCCN3)c3nc2)=O)[o]c2ccccc12 CSIXROXGCKHAKH-BQYQJAHWSA-N 0.000 description 1
- RMQMECKLHVIGEC-CSKARUKUSA-N Cc1c(CN(C)C(/C=C/c2ccc(N)nc2)=O)[nH]c2ccccc12 Chemical compound Cc1c(CN(C)C(/C=C/c2ccc(N)nc2)=O)[nH]c2ccccc12 RMQMECKLHVIGEC-CSKARUKUSA-N 0.000 description 1
- OYVZDKNTKIMYIE-UHFFFAOYSA-N Cc1c(CNC)[nH]c2c1cccc2C(F)(F)F Chemical compound Cc1c(CNC)[nH]c2c1cccc2C(F)(F)F OYVZDKNTKIMYIE-UHFFFAOYSA-N 0.000 description 1
- HTMBBHCSPUIWLJ-UHFFFAOYSA-N Cc1c(CNC)[o]c2c1cccc2 Chemical compound Cc1c(CNC)[o]c2c1cccc2 HTMBBHCSPUIWLJ-UHFFFAOYSA-N 0.000 description 1
- NCSFYRPKSHPTFE-UHFFFAOYSA-N O=C(c([s]c1cccc(F)c11)c1Cl)Cl Chemical compound O=C(c([s]c1cccc(F)c11)c1Cl)Cl NCSFYRPKSHPTFE-UHFFFAOYSA-N 0.000 description 1
- BVSGXWCTWBZFEV-UHFFFAOYSA-N OCc1cccc2c1cc[nH]2 Chemical compound OCc1cccc2c1cc[nH]2 BVSGXWCTWBZFEV-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57694504P | 2004-06-04 | 2004-06-04 | |
| US60/576,945 | 2004-06-04 | ||
| PCT/US2005/019805 WO2007053131A2 (en) | 2004-06-04 | 2005-06-06 | Acrylamide derivatives as antibiotic agents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008505194A JP2008505194A (ja) | 2008-02-21 |
| JP2008505194A5 JP2008505194A5 (https=) | 2012-08-09 |
| JP5087406B2 true JP5087406B2 (ja) | 2012-12-05 |
Family
ID=37889654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007543017A Expired - Fee Related JP5087406B2 (ja) | 2004-06-04 | 2005-06-06 | 治療薬ならびにその製造方法および使用方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US8450307B2 (https=) |
| EP (2) | EP2848614A3 (https=) |
| JP (1) | JP5087406B2 (https=) |
| KR (1) | KR101299399B1 (https=) |
| CA (1) | CA2568914C (https=) |
| CY (1) | CY1115713T1 (https=) |
| DK (1) | DK1828167T3 (https=) |
| ES (1) | ES2515101T3 (https=) |
| PL (1) | PL1828167T3 (https=) |
| PT (1) | PT1828167E (https=) |
| SI (1) | SI1828167T1 (https=) |
| WO (1) | WO2007053131A2 (https=) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU230030B1 (hu) | 1999-10-08 | 2015-05-28 | Debiopharm International Sa | Fab I inhibitorok |
| EP1560584B1 (en) * | 2001-04-06 | 2009-01-14 | Affinium Pharmaceuticals, Inc. | Fab i inhibitors |
| JP5468899B2 (ja) | 2006-07-20 | 2014-04-09 | アフィニウム ファーマシューティカルズ, インク. | Fabiインヒビターとしてのアクリルアミド誘導体 |
| EP2125802A4 (en) | 2007-02-16 | 2014-08-20 | Debiopharm Int Sa | SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS |
| US8569364B2 (en) * | 2007-11-28 | 2013-10-29 | Sequoia Pharmaceuticals, Inc. | 5-substituted benzofurans as inhibitors of cytochrome P450 2D6 |
| US8334236B2 (en) | 2009-02-03 | 2012-12-18 | Kumiai Chemical Industry Co., Ltd. | Ring-fused 2-pyridone derivatives and herbicides |
| WO2011061214A1 (en) | 2009-11-18 | 2011-05-26 | Fab Pharma Sas | Novel heterocyclic acrylamides and their use as pharmaceuticals |
| WO2011131748A2 (en) | 2010-04-21 | 2011-10-27 | Probiodrug Ag | Novel inhibitors |
| HUP1000598A2 (en) | 2010-11-05 | 2012-09-28 | Richter Gedeon Nyrt | Indole derivatives |
| CN103201279A (zh) | 2010-11-05 | 2013-07-10 | 赛诺米克斯公司 | 作为trpm8的调节剂有用的化合物 |
| JO3611B1 (ar) | 2011-08-10 | 2020-08-27 | Janssen Sciences Ireland Uc | سايكلو بنتا (سي (بيرول 4,3 ثاني هيدرو 1 hمستبدله [8,1] نافثيريدينونات مضادة للجراثيم |
| CN105503869A (zh) | 2011-08-10 | 2016-04-20 | 爱尔兰詹森科学公司 | 抗细菌的哌啶基取代的3,4-二氢-1h-[1,8]萘啶酮 |
| US9394295B2 (en) | 2011-08-10 | 2016-07-19 | Janssen Sciences Ireland Uc | Antibacterial homopiperidinyl substituted 3,4-dihydro-1H-[1,8]naphthyridinones |
| CA2849057C (en) * | 2011-09-19 | 2021-05-11 | Vitas Pharma Research Pvt Ltd | Heterocyclic compounds as inhibitors of fatty acid biosynthesis for bacterial infections |
| AU2013279021C1 (en) | 2012-06-19 | 2017-03-16 | Debiopharm International Sa | Prodrug derivatives of (E)-N-methyl-N-((3-methylbenzofuran-2-yl)methyl)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamide |
| JP6250667B2 (ja) * | 2012-08-10 | 2017-12-20 | ヤンセン・サイエンシズ・アイルランド・ユーシー | 新しい抗菌化合物 |
| EP2882739B1 (en) * | 2012-08-10 | 2017-05-03 | Janssen Sciences Ireland UC | New antibacterial compounds |
| WO2014072930A2 (en) * | 2012-11-09 | 2014-05-15 | Aurigene Discovery Technologies Limited | Fused pyridine derivatives as antibacterial agents |
| CN108473484B (zh) | 2015-10-01 | 2021-06-29 | 弗门尼舍公司 | 可用作trpm8调节剂的化合物 |
| RS61312B1 (sr) | 2016-02-26 | 2021-02-26 | Debiopharm Int Sa | Lek za lečenje infekcija dijabetskog stopala |
| SMT202400519T1 (it) * | 2018-11-12 | 2025-01-14 | Debiopharm Int Sa | Composti antibiotici. metodi di produzione degli stessi, composizioni farmaceutiche contenenti gli stessi e loro usi |
| TN2021000159A1 (en) | 2019-02-14 | 2023-04-04 | Debiopharm Int Sa | Afabicin formulation, method for making the same and uses thereof |
| SG11202113174SA (en) | 2019-06-14 | 2021-12-30 | Debiopharm Int Sa | Medicament and use thereof for treating bacterial infections involving biofilm |
| US10947253B2 (en) | 2019-08-05 | 2021-03-16 | Ankh Life Sciences Limited | Fused polycyclic dimers |
| US20230140808A1 (en) * | 2020-04-07 | 2023-05-04 | Sanofi | (1 H-Indol-5-YL)Acrylamide Derivatives as Inhibitors of Tead Proteins and the Hippo-YAP1/TAZ Signaling Cascade for the Treatment of Cancer |
| US20240239771A1 (en) * | 2020-05-29 | 2024-07-18 | Taxis Pharmaceuticals, Inc. | Bacterial efflux pump inhibitors |
| US12129265B2 (en) | 2020-07-21 | 2024-10-29 | Ankh Life Sciences Limited | Therapeutic agents and uses thereof |
| CN111991385A (zh) * | 2020-08-17 | 2020-11-27 | 暨南大学 | 棕榈油酸在抑制水产病原菌中的应用 |
| WO2022187329A1 (en) * | 2021-03-03 | 2022-09-09 | The Board Of Trustees Of The University Of Illinois | Fabi inhibitors for gram-negative pathogens |
| US12060148B2 (en) | 2022-08-16 | 2024-08-13 | Honeywell International Inc. | Ground resonance detection and warning system and method |
| CN121889392A (zh) * | 2023-10-07 | 2026-04-17 | 广州白云山医药集团股份有限公司白云山制药总厂 | 一种FabI酶抑制剂及其应用 |
| WO2025078209A1 (en) * | 2023-10-09 | 2025-04-17 | Debiopharm International S.A. | Antibiotic compounds for treating bacterial infections |
Family Cites Families (117)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3828068A (en) * | 1971-05-10 | 1974-08-06 | Tenneco Chem | ((substituted indazolyl)-n1-methyl)carbamates |
| US4154943A (en) * | 1977-12-29 | 1979-05-15 | University Of Vermont | Preparation of vincadifformine |
| FR2619111B1 (fr) | 1987-08-07 | 1991-01-11 | Synthelabo | Derives de (piperidinyl-4)methyl-2 tetrahydro-1,2,3,4 9h-pyrido (3,4-b) indole, leur preparation et leur application en therapeutique |
| CA2020437A1 (en) | 1989-07-05 | 1991-01-06 | Yoshihide Fuse | Cinnamamide derivative |
| BE1003945A3 (fr) * | 1990-10-04 | 1992-07-22 | Fina Research | Procede de decoloration de polymeres resineux du type vinylaromatique-diene conjugue. |
| HU210679B (en) | 1991-11-21 | 1995-06-28 | Richter Gedeon Vegyeszet | Process for producing new tetrahydro-pyrido/3,4-b/indol derivatives and pharmaceutical compositions containing the same |
| FR2692575B1 (fr) * | 1992-06-23 | 1995-06-30 | Sanofi Elf | Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant. |
| US5416193A (en) * | 1993-04-30 | 1995-05-16 | Pfizer Inc. | Coupling reagent and method |
| US5614551A (en) * | 1994-01-24 | 1997-03-25 | The Johns Hopkins University | Inhibitors of fatty acid synthesis as antimicrobial agents |
| US6176842B1 (en) | 1995-03-08 | 2001-01-23 | Ekos Corporation | Ultrasound assembly for use with light activated drugs |
| US5989832A (en) | 1995-04-21 | 1999-11-23 | Microcide Pharmaceuticals, Inc. | Method for screening for non-tetracycline efflux pump inhibitors |
| SK284962B6 (sk) * | 1995-05-11 | 2006-03-02 | Sandoz Ag | 7-Acylamino-3-(hydrazono)metylcefalosporíny, spôsob ich prípravy, medziprodukty na ich prípravu a farmaceutický prostriedok, ktorý ich obsahuje |
| US6057291A (en) * | 1995-06-02 | 2000-05-02 | University Of British Columbia | Antimicrobial cationic peptides |
| ATE216887T1 (de) * | 1996-02-29 | 2002-05-15 | Fujisawa Pharmaceutical Co | Beta-lactam-antibiotikum enthaltende tabletten und verfahren zu deren herstellung |
| US6239154B1 (en) | 1996-03-08 | 2001-05-29 | Adolor Corporation | Kappa agonist compounds pharmaceutical formulations and method of prevention and treatment of pruritus therewith |
| US6367985B1 (en) * | 1996-03-12 | 2002-04-09 | Intellectual Property Company | Optical connector using large diameter alignment features |
| US6451816B1 (en) * | 1997-06-20 | 2002-09-17 | Klinge Pharma Gmbh | Use of pyridyl alkane, pyridyl alkene and/or pyridyl alkine acid amides in the treatment of tumors or for immunosuppression |
| JPH1023696A (ja) * | 1996-07-01 | 1998-01-23 | Sankyo Seiki Mfg Co Ltd | スピンドルモータおよびその製造方法 |
| US6503881B2 (en) | 1996-08-21 | 2003-01-07 | Micrologix Biotech Inc. | Compositions and methods for treating infections using cationic peptides alone or in combination with antibiotics |
| US6995254B1 (en) * | 1996-08-28 | 2006-02-07 | Affinium Pharmaceuticals, Inc. | Polynucleotide encoding the enoyl-acyl carrier protein reductase of Staphylococcus aureus, FAB I |
| WO1998012200A1 (en) | 1996-09-20 | 1998-03-26 | Meiji Seika Kaisha Ltd. | A crystalline substance of cefditoren pivoxyl and the production of the same |
| US6521408B1 (en) | 1997-09-25 | 2003-02-18 | National Institute Of Agrobiological Sciences | Method for assessing a function of a gene |
| DE19641437A1 (de) | 1996-10-08 | 1998-04-09 | Basf Ag | 1,3-Bis-(N-lactamyl)propane und deren pharmazeutische und kosmetische Verwendung |
| DE19652239A1 (de) * | 1996-12-16 | 1998-06-18 | Bayer Ag | Verwendung von 7-(2-Oxa-5,8-diazabicyclo[4.3.0]non-8-yl)-chinolon- und -naphthyridoncarbonsäure-Derivaten zur Therapie von Helicobacter-pylori-Infektionen und den damit assoziierten gastroduodenalen Erkrankungen |
| SI9600371B (sl) | 1996-12-18 | 2005-04-30 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | Etilidenski derivati tricikličnih karbapenemov |
| AU6870098A (en) | 1997-03-31 | 1998-10-22 | Du Pont Merck Pharmaceutical Company, The | Indazoles of cyclic ureas useful as hiv protease inhibitors |
| EP0971735B1 (en) | 1997-04-01 | 2008-03-19 | Thomas Julius Borody | Methods and compositions for treating inflammatory bowel disease |
| US6406880B1 (en) * | 1997-05-02 | 2002-06-18 | Integrated Research Technology, Llc | Betaines as adjuvants to susceptibility testing and antimicrobial therapy |
| US6184363B1 (en) * | 1997-06-13 | 2001-02-06 | Northwestern University | Inhibitors of β-lactamases and uses therefor |
| KR20010014105A (ko) * | 1997-06-23 | 2001-02-26 | 가마쿠라 아키오 | 헬리코박터 감염에 기인한 질환의 예방 또는 치료제 |
| AUPO758297A0 (en) * | 1997-06-27 | 1997-07-24 | Rowe, James Baber | Control of acidic gut syndrome |
| US6198000B1 (en) * | 1997-07-07 | 2001-03-06 | Pfizer Inc. | Intermediates useful in the synthesis of quinoline antibiotics |
| US6313153B1 (en) | 1997-07-25 | 2001-11-06 | Tsumura & Co. | Compositions and methods for treating nephritis and inhibiting TGF -β related conditions using pyridylacrylamide derivatives |
| HN1998000106A (es) * | 1997-08-01 | 1999-01-08 | Pfizer Prod Inc | Composiciones parenterales de alatroflaxacino |
| US5932743A (en) * | 1997-08-21 | 1999-08-03 | American Home Products Corporation | Methods for the solid phase synthesis of substituted indole compounds |
| GB9717804D0 (en) | 1997-08-22 | 1997-10-29 | Zeneca Ltd | Chemical compounds |
| JP2001503280A (ja) | 1997-10-31 | 2001-03-13 | ノバルティス アクチエンゲゼルシャフト | グリフォセート耐性トランスジェニック植物 |
| US6432444B1 (en) | 1997-10-31 | 2002-08-13 | New Horizons Diagnostics Corp | Use of bacterial phage associated lysing enzymes for treating dermatological infections |
| SE9704404D0 (sv) * | 1997-11-28 | 1997-11-28 | Astra Ab | New compounds |
| GB9725244D0 (en) | 1997-11-29 | 1998-01-28 | Zeneca Ltd | Chemical compounds |
| DE19753298A1 (de) * | 1997-12-01 | 1999-06-02 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
| HU230295B1 (hu) | 1998-01-07 | 2015-12-28 | Meiji Seika Pharma Co., Ltd. | Kristálytanilag stabil, amorf, cephalosporin tartalmú készítmény és eljárás előállítására |
| US6184380B1 (en) | 1999-01-25 | 2001-02-06 | Pfizer Inc. | Process for preparing naphthyridones and intermediates |
| PA8466701A1 (es) | 1998-01-21 | 2000-09-29 | Pfizer Prod Inc | Comprimido de mesilato de trovafloxacino |
| US6204279B1 (en) | 1998-06-03 | 2001-03-20 | Microcide Pharmaceuticals, Inc. | Peptidomimetic efflux pump inhibitors |
| BRPI9908182C1 (pt) | 1998-02-27 | 2021-05-25 | Biora Ab | composições de proteína de matriz para cura de feridas |
| US6350738B1 (en) | 1998-03-06 | 2002-02-26 | Brigham Young University | Steroid derived antibiotics |
| DE19820801A1 (de) * | 1998-05-09 | 1999-11-25 | Gruenenthal Gmbh | Orale Arzneiformen mit reproduzierbarer Wirkstofffreisetzung von Gatifloxacin oder pharmazeutisch verwendbaren Salzen oder Hydraten |
| DE19821039A1 (de) | 1998-05-11 | 1999-11-18 | Bayer Ag | Verfahren zur Herstellung von (S,S)-Benzyl-2,8-diazabicyclo[4.3.0]nonan |
| US6399629B1 (en) | 1998-06-01 | 2002-06-04 | Microcide Pharmaceuticals, Inc. | Efflux pump inhibitors |
| US6428579B1 (en) * | 1998-07-01 | 2002-08-06 | Brown University Research Foundation | Implantable prosthetic devices coated with bioactive molecules |
| US6423741B1 (en) | 1998-07-10 | 2002-07-23 | Council Of Scientific And Industrial Research | Anti-microbial composition and method for producing the same |
| GB9815567D0 (en) * | 1998-07-18 | 1998-09-16 | Glaxo Group Ltd | Antiviral compound |
| ATE386546T1 (de) * | 1998-08-04 | 2008-03-15 | Takeda Schering Plough Animal | Stabilisierte ölige zubereitung von tobicillin (beta-lactam-antibiotika) |
| KR100595956B1 (ko) | 1998-08-21 | 2006-07-03 | 센주 세이야꾸 가부시키가이샤 | 수성액 제약학적 조성물 |
| US6461607B1 (en) | 1998-08-24 | 2002-10-08 | Ganeden Biotech, Inc. | Probiotic, lactic acid-producing bacteria and uses thereof |
| US6518487B1 (en) | 1998-09-23 | 2003-02-11 | Pioneer Hi-Bred International, Inc. | Cyclin D polynucleotides, polypeptides and uses thereof |
| US6395746B1 (en) * | 1998-09-30 | 2002-05-28 | Alcon Manufacturing, Ltd. | Methods of treating ophthalmic, otic and nasal infections and attendant inflammation |
| US6509327B1 (en) * | 1998-09-30 | 2003-01-21 | Alcon Manufacturing, Ltd. | Compositions and methods for treating otic, ophthalmic and nasal infections |
| DE19851104C2 (de) | 1998-11-06 | 2003-04-03 | Huhtamaki Forchheim | Verfahren zum Herstellen eines mehrschichtigen Verbundes |
| TW526202B (en) | 1998-11-27 | 2003-04-01 | Shionogi & Amp Co | Broad spectrum cephem having benzo[4,5-b]pyridium methyl group of antibiotic activity |
| CA2371816C (en) * | 1999-02-18 | 2010-04-27 | The Regents Of The University Of California | Phthalamide-lanthanide complexes for use as luminescent markers |
| US6248363B1 (en) | 1999-11-23 | 2001-06-19 | Lipocine, Inc. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| US6267985B1 (en) | 1999-06-30 | 2001-07-31 | Lipocine Inc. | Clear oil-containing pharmaceutical compositions |
| US6294192B1 (en) * | 1999-02-26 | 2001-09-25 | Lipocine, Inc. | Triglyceride-free compositions and methods for improved delivery of hydrophobic therapeutic agents |
| AU3615200A (en) | 1999-03-03 | 2000-09-21 | Princeton University | Bacterial transglycosylases: assays for monitoring the activity using lipid ii substrate analogs and methods for discovering new antibiotics |
| US6495161B1 (en) | 1999-03-09 | 2002-12-17 | Vivorx, Inc. | Cytoprotective biocompatible containment systems for biologically active materials and methods of making same |
| US6239113B1 (en) | 1999-03-31 | 2001-05-29 | Insite Vision, Incorporated | Topical treatment or prevention of ocular infections |
| US6448054B1 (en) * | 1999-04-08 | 2002-09-10 | The General Hospital Corporation | Purposeful movement of human migratory cells away from an agent source |
| CO5180550A1 (es) | 1999-04-19 | 2002-07-30 | Smithkline Beecham Corp | Inhibidores de fab i |
| US6290946B1 (en) | 1999-05-13 | 2001-09-18 | Geltex Pharmaceuticals, Inc. | Anionic polymers as toxin binders and antibacterial agents |
| US6514535B2 (en) * | 1999-05-21 | 2003-02-04 | Noveon Ip Holdings Corp. | Bioadhesive hydrogels with functionalized degradable crosslinks |
| AR024077A1 (es) * | 1999-05-25 | 2002-09-04 | Smithkline Beecham Corp | Compuestos antibacterianos |
| CO5370679A1 (es) | 1999-06-01 | 2004-02-27 | Smithkline Beecham Corp | Inhibidores fab 1 |
| US6239141B1 (en) * | 1999-06-04 | 2001-05-29 | Pfizer Inc. | Trovafloxacin oral suspensions |
| CO5180605A1 (es) * | 1999-06-23 | 2002-07-30 | Smithkline Beecham Corp | Compuestos de indol |
| CA2282066C (en) * | 1999-06-29 | 2010-09-07 | Smithkline Beecham Corporation | Methods of use of quinolone compounds against atypical upper respiratory pathogenic bacteria |
| US6309663B1 (en) | 1999-08-17 | 2001-10-30 | Lipocine Inc. | Triglyceride-free compositions and methods for enhanced absorption of hydrophilic therapeutic agents |
| US6500459B1 (en) | 1999-07-21 | 2002-12-31 | Harinderpal Chhabra | Controlled onset and sustained release dosage forms and the preparation thereof |
| US6346391B1 (en) | 1999-07-22 | 2002-02-12 | Trustees Of Tufts College | Methods of reducing microbial resistance to drugs |
| EP1212093B1 (en) | 1999-08-26 | 2004-07-07 | Ganeden Biotech, Inc. | Use of emu oil as a carrier for antifungal, antibacterial and antiviral medications |
| US6221859B1 (en) | 1999-08-27 | 2001-04-24 | Merck & Co., Inc. | Carbapenem antibacterial compositions and methods of the treatment |
| US6174878B1 (en) | 1999-08-31 | 2001-01-16 | Alcon Laboratories, Inc. | Topical use of kappa opioid agonists to treat otic pain |
| ES2282134T3 (es) | 1999-09-11 | 2007-10-16 | THE PROCTER & GAMBLE COMPANY | Copolimeros de polioxialquileno que contienen vehiculos liquidos fluidos. |
| CN1198611C (zh) | 1999-09-17 | 2005-04-27 | 第一三得利制药株式会社 | 药物抗菌剂组合物 |
| US6500463B1 (en) | 1999-10-01 | 2002-12-31 | General Mills, Inc. | Encapsulation of sensitive components into a matrix to obtain discrete shelf-stable particles |
| US6730684B1 (en) * | 1999-10-08 | 2004-05-04 | Affinium Pharmaceuticals, Inc. | Fab I inhibitors |
| HU230030B1 (hu) * | 1999-10-08 | 2015-05-28 | Debiopharm International Sa | Fab I inhibitorok |
| US6762201B1 (en) * | 1999-10-08 | 2004-07-13 | Affinium Pharmaceuticals, Inc. | Fab I inhibitors |
| US6503908B1 (en) * | 1999-10-11 | 2003-01-07 | Pfizer Inc | Pharmaceutically active compounds |
| EP1227096B1 (en) * | 1999-10-19 | 2004-09-22 | Sato Pharmaceutical Co. Ltd. | 4-oxoquinolizine antimicrobials having 2-pyridone skeletons as the partial structure |
| US6951729B1 (en) * | 1999-10-27 | 2005-10-04 | Affinium Pharmaceuticals, Inc. | High throughput screening method for biological agents affecting fatty acid biosynthesis |
| NZ518401A (en) * | 1999-10-29 | 2004-01-30 | Nektar Therapeutics | Dry powder compositions having improved dispersivity |
| US6531291B1 (en) * | 1999-11-10 | 2003-03-11 | The Trustees Of Columbia University In The City Of New York | Antimicrobial activity of gemfibrozil and related compounds and derivatives and metabolites thereof |
| US6514986B2 (en) | 2000-11-22 | 2003-02-04 | Wockhardt Limited | Chiral fluoroquinolone arginine salt forms |
| US6372752B1 (en) * | 2000-02-07 | 2002-04-16 | Genzyme Corporation | Inha inhibitors and methods of use thereof |
| AU2000255628A1 (en) * | 2000-03-28 | 2001-10-08 | Council Of Scientific And Industrial Research | Formulation comprising thymol useful in the treatment of drug resistant bacterial infections |
| EP1280753A1 (en) | 2000-04-21 | 2003-02-05 | Rhodia/Chirex, Inc. | Process for preparation of r-1-(aryloxy)propan-2-ol |
| AU2001282988B2 (en) * | 2000-07-26 | 2006-01-05 | Atopic Pty Ltd | Methods for treating atopic disorders |
| DE10037029A1 (de) | 2000-07-27 | 2002-02-28 | Kugelstrahlzentrum Aachen Gmbh | Verfahren und Vorrichtung zum Umformen von Strukturbauteilen |
| US6288239B1 (en) * | 2000-09-19 | 2001-09-11 | Board Of Trustees Operating Michigan State University | 5-trityloxymethyl-oxazolidinones and process for the preparation thereof |
| US6821746B2 (en) | 2000-10-06 | 2004-11-23 | Affinium Pharmaceuticals, Inc. | Methods of screening for FabK antagonists and agonists |
| US7048926B2 (en) * | 2000-10-06 | 2006-05-23 | Affinium Pharmaceuticals, Inc. | Methods of agonizing and antagonizing FabK |
| WO2002031128A1 (en) * | 2000-10-06 | 2002-04-18 | Smithkline Beecham Corporation | Methods of agonizing and antagonizing fabk |
| US6388070B1 (en) | 2001-01-05 | 2002-05-14 | Orchid Chemicals & Pharmaceuticals Ltd. | Thioester derivatives of thiazolyl acetic acid and their use in the preparation of cephalosporin compounds |
| US6495158B1 (en) | 2001-01-19 | 2002-12-17 | Lec Tec Corporation | Acne patch |
| EP1560584B1 (en) * | 2001-04-06 | 2009-01-14 | Affinium Pharmaceuticals, Inc. | Fab i inhibitors |
| US6503906B1 (en) * | 2002-02-21 | 2003-01-07 | Ren-Jin Lee | Method for optimizing ciprofloxacin treatment of anthrax-exposed patients according to the patient's characteristics |
| EP1575951B1 (en) * | 2002-12-06 | 2014-06-25 | Debiopharm International SA | Heterocyclic compounds, methods of making them and their use in therapy |
| WO2004082586A2 (en) * | 2003-03-17 | 2004-09-30 | Affinium Pharmaceuticals, Inc. | Phamaceutical compositions comprising inhibitors of fab i and further antibiotics |
| KR20080075027A (ko) * | 2005-12-05 | 2008-08-13 | 아피늄 파마슈티컬스, 인크. | Fabi 억제제 및 항박테리아제로서의헤테로시클릴아크릴아미드 화합물 |
| JP5468899B2 (ja) | 2006-07-20 | 2014-04-09 | アフィニウム ファーマシューティカルズ, インク. | Fabiインヒビターとしてのアクリルアミド誘導体 |
| EP2125802A4 (en) * | 2007-02-16 | 2014-08-20 | Debiopharm Int Sa | SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS |
| WO2010117920A1 (en) | 2009-04-08 | 2010-10-14 | C&D Zodiac, Inc. | Vehicle seat tubing having variable wall thickness |
| JP6013846B2 (ja) | 2011-10-06 | 2016-10-25 | リコー電子デバイス株式会社 | スイッチングレギュレータ及び電子機器 |
| US8975502B1 (en) | 2012-05-15 | 2015-03-10 | Rodulfo Delgado | Guitar with body-mounted tuning system |
| US8973902B2 (en) | 2012-12-21 | 2015-03-10 | Comeup Industries Inc. | Power winch horizontal-pull clutch device |
-
2005
- 2005-06-06 DK DK05858503.5T patent/DK1828167T3/da active
- 2005-06-06 JP JP2007543017A patent/JP5087406B2/ja not_active Expired - Fee Related
- 2005-06-06 PL PL05858503T patent/PL1828167T3/pl unknown
- 2005-06-06 KR KR1020077000169A patent/KR101299399B1/ko not_active Expired - Fee Related
- 2005-06-06 ES ES05858503.5T patent/ES2515101T3/es not_active Expired - Lifetime
- 2005-06-06 EP EP14179596.3A patent/EP2848614A3/en not_active Withdrawn
- 2005-06-06 PT PT58585035T patent/PT1828167E/pt unknown
- 2005-06-06 SI SI200531900T patent/SI1828167T1/sl unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| DK1828167T3 (da) | 2014-10-20 |
| EP2848614A3 (en) | 2015-07-29 |
| JP2008505194A (ja) | 2008-02-21 |
| WO2007053131A2 (en) | 2007-05-10 |
| PT1828167E (pt) | 2014-10-08 |
| KR20080016517A (ko) | 2008-02-21 |
| EP1828167B1 (en) | 2014-08-06 |
| ES2515101T3 (es) | 2014-10-29 |
| CA2568914A1 (en) | 2005-12-04 |
| KR101299399B1 (ko) | 2013-08-22 |
| EP1828167A2 (en) | 2007-09-05 |
| US20100093705A1 (en) | 2010-04-15 |
| PL1828167T3 (pl) | 2015-02-27 |
| CA2568914C (en) | 2013-09-24 |
| US8450307B2 (en) | 2013-05-28 |
| WO2007053131A3 (en) | 2007-08-02 |
| US20140107106A1 (en) | 2014-04-17 |
| SI1828167T1 (sl) | 2014-12-31 |
| CY1115713T1 (el) | 2017-01-25 |
| EP2848614A2 (en) | 2015-03-18 |
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