JP2012502957A5 - - Google Patents
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- Publication number
- JP2012502957A5 JP2012502957A5 JP2011527334A JP2011527334A JP2012502957A5 JP 2012502957 A5 JP2012502957 A5 JP 2012502957A5 JP 2011527334 A JP2011527334 A JP 2011527334A JP 2011527334 A JP2011527334 A JP 2011527334A JP 2012502957 A5 JP2012502957 A5 JP 2012502957A5
- Authority
- JP
- Japan
- Prior art keywords
- amino
- phenyl
- trifluoromethyl
- thiazol
- propanoic 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 11
- -1 C 1 -C 4 - alkoxy Chemical group 0.000 claims 7
- 125000005843 halogen group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- OUGCUPYREMACGK-ZETCQYMHSA-N (2s)-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 OUGCUPYREMACGK-ZETCQYMHSA-N 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 229940124530 sulfonamide Drugs 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- JTCRRKHXSLUWCW-RYUDHWBXSA-N (2S)-N-[(2S)-3-methylbutan-2-yl]-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanamide Chemical compound CC([C@H](C)NC([C@@H](C)C1=CC=C(C=C1)NC=1SC=C(N1)C(F)(F)F)=O)C JTCRRKHXSLUWCW-RYUDHWBXSA-N 0.000 claims 1
- LPPNMWHZIUTUIZ-SSDOTTSWSA-N (2r)-2-[4-[[4-(trifluoromethyl)-1,3-oxazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC([C@H](C(O)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CO1 LPPNMWHZIUTUIZ-SSDOTTSWSA-N 0.000 claims 1
- FMOLJMSMIBIXIA-DTWKUNHWSA-N (2r)-2-[[(2s)-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoyl]amino]propanoic acid Chemical compound C1=CC([C@H](C)C(=O)N[C@H](C)C(O)=O)=CC=C1NC1=NC(C(F)(F)F)=CS1 FMOLJMSMIBIXIA-DTWKUNHWSA-N 0.000 claims 1
- FDCNKYFUHVZCSP-VIFPVBQESA-N (2s)-2-[4-[(4-methyl-1,3-thiazol-2-yl)amino]phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1NC1=NC(C)=CS1 FDCNKYFUHVZCSP-VIFPVBQESA-N 0.000 claims 1
- NLXCGSIYDLCURI-JTQLQIEISA-N (2s)-2-[4-[(4-tert-butyl-1,3-thiazol-2-yl)amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(N)=O)C)=CC=C1NC1=NC(C(C)(C)C)=CS1 NLXCGSIYDLCURI-JTQLQIEISA-N 0.000 claims 1
- PEWMCDTVGCALBX-JTQLQIEISA-N (2s)-2-[4-[(4-tert-butyl-1,3-thiazol-2-yl)amino]phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1NC1=NC(C(C)(C)C)=CS1 PEWMCDTVGCALBX-JTQLQIEISA-N 0.000 claims 1
- LOHRBNWFZDNPBQ-ZETCQYMHSA-N (2s)-2-[4-[[4-(trifluoromethyl)-1,3-oxazol-2-yl]amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(N)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CO1 LOHRBNWFZDNPBQ-ZETCQYMHSA-N 0.000 claims 1
- HOMUGWXASAQAJZ-ZETCQYMHSA-N (2s)-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(N)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 HOMUGWXASAQAJZ-ZETCQYMHSA-N 0.000 claims 1
- HAYVAQQHDVELQB-QMMMGPOBSA-N (2s)-2-[4-[methyl-[4-(trifluoromethyl)-1,3-oxazol-2-yl]amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(N)=O)C)=CC=C1N(C)C1=NC(C(F)(F)F)=CO1 HAYVAQQHDVELQB-QMMMGPOBSA-N 0.000 claims 1
- SBHOTKAIHLCPME-QMMMGPOBSA-N (2s)-2-[4-[methyl-[4-(trifluoromethyl)-1,3-oxazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1N(C)C1=NC(C(F)(F)F)=CO1 SBHOTKAIHLCPME-QMMMGPOBSA-N 0.000 claims 1
- JPNWKDQSTHQRNB-QMMMGPOBSA-N (2s)-2-[4-[methyl-[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(N)=O)C)=CC=C1N(C)C1=NC(C(F)(F)F)=CS1 JPNWKDQSTHQRNB-QMMMGPOBSA-N 0.000 claims 1
- FQTRGPOTTZHVLU-QMMMGPOBSA-N (2s)-2-[4-[methyl-[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1N(C)C1=NC(C(F)(F)F)=CS1 FQTRGPOTTZHVLU-QMMMGPOBSA-N 0.000 claims 1
- GQTBSMGULLZWIP-IUCAKERBSA-N (2s)-2-[[(2s)-2-[4-[[4-(trifluoromethyl)-1,3-oxazol-2-yl]amino]phenyl]propanoyl]amino]propanoic acid Chemical compound C1=CC([C@H](C)C(=O)N[C@@H](C)C(O)=O)=CC=C1NC1=NC(C(F)(F)F)=CO1 GQTBSMGULLZWIP-IUCAKERBSA-N 0.000 claims 1
- XZSNMIFWZAAWAV-ZETCQYMHSA-N (2s)-n-hydroxy-2-[4-[[4-(trifluoromethyl)-1,3-oxazol-2-yl]amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(=O)NO)C)=CC=C1NC1=NC(C(F)(F)F)=CO1 XZSNMIFWZAAWAV-ZETCQYMHSA-N 0.000 claims 1
- QIAMDXLMJHYOGF-QMMMGPOBSA-N (2s)-n-methylsulfonyl-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanamide Chemical compound C1=CC([C@@H](C(=O)NS(C)(=O)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 QIAMDXLMJHYOGF-QMMMGPOBSA-N 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- FDCNKYFUHVZCSP-UHFFFAOYSA-N 2-[4-[(4-methyl-1,3-thiazol-2-yl)amino]phenyl]propanoic acid Chemical compound C1=CC(C(C(O)=O)C)=CC=C1NC1=NC(C)=CS1 FDCNKYFUHVZCSP-UHFFFAOYSA-N 0.000 claims 1
- PEWMCDTVGCALBX-UHFFFAOYSA-N 2-[4-[(4-tert-butyl-1,3-thiazol-2-yl)amino]phenyl]propanoic acid Chemical compound C1=CC(C(C(O)=O)C)=CC=C1NC1=NC(C(C)(C)C)=CS1 PEWMCDTVGCALBX-UHFFFAOYSA-N 0.000 claims 1
- OUGCUPYREMACGK-UHFFFAOYSA-N 2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC(C(C(O)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 OUGCUPYREMACGK-UHFFFAOYSA-N 0.000 claims 1
- FQTRGPOTTZHVLU-UHFFFAOYSA-N 2-[4-[methyl-[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC(C(C(O)=O)C)=CC=C1N(C)C1=NC(C(F)(F)F)=CS1 FQTRGPOTTZHVLU-UHFFFAOYSA-N 0.000 claims 1
- TVKXUJXIOMUVFS-UHFFFAOYSA-N 2-methyl-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 TVKXUJXIOMUVFS-UHFFFAOYSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 206010016654 Fibrosis Diseases 0.000 claims 1
- 206010018364 Glomerulonephritis Diseases 0.000 claims 1
- 101001055222 Homo sapiens Interleukin-8 Proteins 0.000 claims 1
- 102100026236 Interleukin-8 Human genes 0.000 claims 1
- 206010034277 Pemphigoid Diseases 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 208000000594 bullous pemphigoid Diseases 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 230000035605 chemotaxis Effects 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 230000004761 fibrosis Effects 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 208000028867 ischemia Diseases 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- LKJVHRADKSYPEM-ZETCQYMHSA-N methyl (2s)-2-[4-(carbamothioylamino)phenyl]propanoate Chemical compound COC(=O)[C@@H](C)C1=CC=C(NC(N)=S)C=C1 LKJVHRADKSYPEM-ZETCQYMHSA-N 0.000 claims 1
- HXAMUXFIQLEMOM-ZETCQYMHSA-N methyl (2s)-2-[4-(carbamoylamino)phenyl]propanoate Chemical compound COC(=O)[C@@H](C)C1=CC=C(NC(N)=O)C=C1 HXAMUXFIQLEMOM-ZETCQYMHSA-N 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000003884 phenylalkyl group Chemical group 0.000 claims 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims 1
- 230000010410 reperfusion Effects 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- QCZUONQLUCNBKS-FJXQXJEOSA-M sodium;(2s)-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoate Chemical compound [Na+].C1=CC([C@@H](C([O-])=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 QCZUONQLUCNBKS-FJXQXJEOSA-M 0.000 claims 1
- 150000003456 sulfonamides Chemical class 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 201000010875 transient cerebral ischemia Diseases 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08164605.1 | 2008-09-18 | ||
| EP08164605A EP2166006A1 (en) | 2008-09-18 | 2008-09-18 | 2-aryl-propionic acids and derivatives and pharmaceutical compositions containing them |
| PCT/EP2009/062109 WO2010031835A2 (en) | 2008-09-18 | 2009-09-18 | 2-aryl-propionic acids and derivatives and pharmaceutical compositions containing them |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012502957A JP2012502957A (ja) | 2012-02-02 |
| JP2012502957A5 true JP2012502957A5 (enExample) | 2012-11-08 |
| JP5571669B2 JP5571669B2 (ja) | 2014-08-13 |
Family
ID=40291117
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011527334A Active JP5571669B2 (ja) | 2008-09-18 | 2009-09-18 | ２−アリール−プロピオン酸及び誘導体、並びにそれらを含有する医薬組成物 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8624036B2 (enExample) |
| EP (2) | EP2166006A1 (enExample) |
| JP (1) | JP5571669B2 (enExample) |
| CN (1) | CN102159558B (enExample) |
| AU (1) | AU2009294558B2 (enExample) |
| CA (1) | CA2737099C (enExample) |
| CY (1) | CY1116176T1 (enExample) |
| DK (1) | DK2346841T3 (enExample) |
| ES (1) | ES2534634T3 (enExample) |
| HR (1) | HRP20150395T1 (enExample) |
| IL (1) | IL211683A (enExample) |
| PL (1) | PL2346841T3 (enExample) |
| PT (1) | PT2346841E (enExample) |
| RU (1) | RU2520212C2 (enExample) |
| SI (1) | SI2346841T1 (enExample) |
| SM (1) | SMT201500098B (enExample) |
| WO (1) | WO2010031835A2 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2634185T3 (pl) | 2012-03-02 | 2016-06-30 | Sareum Ltd | Inhibitory kinazy TYK2 |
| US10046002B2 (en) | 2013-08-02 | 2018-08-14 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists |
| US10561676B2 (en) * | 2013-08-02 | 2020-02-18 | Syntrix Biosystems Inc. | Method for treating cancer using dual antagonists of CXCR1 and CXCR2 |
| KR102191084B1 (ko) * | 2013-09-03 | 2020-12-15 | 사름 리미티드 | 약제학적 화합물 |
| AR103399A1 (es) * | 2015-01-15 | 2017-05-10 | Actelion Pharmaceuticals Ltd | Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3 |
| EP3117835A1 (en) * | 2015-07-14 | 2017-01-18 | Dompé farmaceutici s.p.a. | Il-8 inhibitors for use in the treatment of certain urological disorders |
| SG11201804484YA (en) | 2016-01-15 | 2018-07-30 | Dompe Farm Spa | Il-8 inhibitors for use in the treatment of chemotherapy-induced peripheral neuropathy |
| EP3192504A1 (en) | 2016-01-15 | 2017-07-19 | Dompé farmaceutici S.p.A. | Il-8 inhibitors for use in the treatment of chemotherapy-induced peripheral neuropathy |
| US11291641B2 (en) | 2016-10-03 | 2022-04-05 | The Children's Medical Center Corporation | Prevention and treatment of diabetic nephropathy |
| GB201617871D0 (en) | 2016-10-21 | 2016-12-07 | Sareum Limited | Pharmaceutical compounds |
| US10660909B2 (en) | 2016-11-17 | 2020-05-26 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists |
| EP3342407A1 (en) * | 2017-01-03 | 2018-07-04 | Dompé farmaceutici S.p.A. | Il-8 inihibitors for use in the treatment of some urological disorders |
| EP3409277A1 (en) * | 2017-05-30 | 2018-12-05 | Dompé farmaceutici s.p.a. | Il-8 inhibitors for use in the treatment and/or prevention of bacterial secondary infections |
| EP3476390A1 (en) | 2017-10-24 | 2019-05-01 | Dompé farmaceutici S.p.A. | Il-8 inhibitors for use in the treatment of sarcomas |
| WO2019165315A1 (en) | 2018-02-23 | 2019-08-29 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists alone or in combination |
| GB201816369D0 (en) | 2018-10-08 | 2018-11-28 | Sareum Ltd | Pharmaceutical compounds |
| EP3868369A1 (en) | 2020-02-21 | 2021-08-25 | Dompe' Farmaceutici S.P.A. | Cxcl8 inhibitor and pharmaceutical composition thereof for use in the treatment of cancer-related fatigue |
| EP3868368A1 (en) | 2020-02-21 | 2021-08-25 | Dompe' Farmaceutici S.P.A. | Cxcl8 (interleukin-8) activity inhibitor and corticosteroid combination and pharmaceutical composition and use thereof |
| EP3884932A1 (en) | 2020-03-26 | 2021-09-29 | Dompe' Farmaceutici S.P.A. | Cxcl8 inhibitors for use in the treatment of covid-19 |
| CN115397404A (zh) | 2020-03-26 | 2022-11-25 | 东佩制药股份公司 | 用于治疗covid-19的cxcl8抑制剂 |
| EP4008325A1 (en) | 2020-12-02 | 2022-06-08 | Dompe' Farmaceutici S.P.A. | Cxcl8 inhibitors for use in the treatment of covid-19 |
| EP3907214A1 (en) * | 2020-05-04 | 2021-11-10 | Dompe' Farmaceutici S.P.A. | Co-crystal of ketoprofen, lysine and gabapentin, pharmaceutical compositions and their medical use |
| WO2022098822A1 (en) | 2020-11-05 | 2022-05-12 | Icahn School Of Medicine At Mount Sinai | Cxcr1/cxcr2 inhibitors for use in treating myelofibrosis |
| EP4052702A1 (en) | 2021-03-04 | 2022-09-07 | Dompé farmaceutici S.p.a. | Cxcl8 inhibitor and pharmaceutical composition thereof for use in the treatment of seizures |
| EP4397305A1 (en) | 2023-01-05 | 2024-07-10 | Dompe' Farmaceutici S.P.A. | Cxcl8 inhibitors for use in the treatment of ocular mucous membrane pemphigoid and/or oral mucous membrane pemphigoid |
| EP4406942A1 (en) * | 2023-01-26 | 2024-07-31 | Dompe' Farmaceutici S.P.A. | Stable monohydrate of df2755a and process for its preparation |
| EP4563594A1 (en) | 2023-11-28 | 2025-06-04 | Dompe' Farmaceutici SpA | Cxcl8 inhibitors for use in the treatment of tumors with low stromal cav1 levels |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1051906A (en) * | 1973-10-24 | 1979-04-03 | Shionogi And Co. | Thiazole derivatives and production thereof |
| JPS5537556B2 (enExample) * | 1973-12-27 | 1980-09-29 | ||
| US4025528A (en) * | 1973-10-24 | 1977-05-24 | Shionogi & Co., Ltd. | Thiazole derivatives of benzoic and phenylalkanoic acids |
| JPS565747B2 (enExample) * | 1973-10-24 | 1981-02-06 | ||
| JPS5629871B2 (enExample) * | 1974-05-22 | 1981-07-10 | ||
| JPS62142168A (ja) * | 1985-10-16 | 1987-06-25 | Mitsubishi Chem Ind Ltd | チアゾ−ル誘導体及びそれを有効成分とするロイコトリエンきつ抗剤 |
| IT1298214B1 (it) | 1998-01-28 | 1999-12-20 | Dompe Spa | Sali dell'acido (r) 2-(3-benzoilfenil) propionico e loro composizioni farmaceutiche. |
| IT1303249B1 (it) * | 1998-10-23 | 2000-11-06 | Dompe Spa | Alcune n-(2-aril-propionil)-solfonammidi e preparazionifarmaceutiche che le contengono. |
| IT1317826B1 (it) | 2000-02-11 | 2003-07-15 | Dompe Spa | Ammidi, utili nell'inibizione della chemiotassi dei neutrofiliindotta da il-8. |
| ITMI20012434A1 (it) | 2001-11-20 | 2003-05-20 | Dompe Spa | Acidi 2-aril-propionici e composizioni farmaceutiche che li contengono |
| WO2003062215A1 (en) * | 2002-01-25 | 2003-07-31 | Kylix Pharmaceuticals B.V. | 4(hetero-) aryl substituted (thia-/oxa-/pyra) zoles for inhibition of tie-2 |
| DE602005016937D1 (de) * | 2004-03-23 | 2009-11-12 | Dompe Pha R Ma Spa Res & Mfg | Pharmazeutische zusammensetzung |
| HRP20161260T1 (hr) * | 2005-11-24 | 2016-11-18 | Dompé Farmaceutici S.P.A. | Derivati (r)-arilkilamina i farmaceutski pripravci koji ih sadrže |
| AU2007253424B2 (en) * | 2006-05-18 | 2013-03-07 | Dompe' Farmaceutici S.P.A. | (2R)-2-[(4-sulfonyl)aminophenyl]propanamides and pharmaceutical compositions containing them |
| ES2394641T3 (es) * | 2006-12-19 | 2013-02-04 | Dompe' S.P.A. | Ácidos 2-aril-2-fluoropropanoicos y derivados y composiciones farmacéuticas que los contienen |
| DE602008005488D1 (de) * | 2007-10-18 | 2011-04-21 | Dompe Spa | (r)-4-(heteroaryl)phenylethylderivate und pharmazeutische zusammensetzungen damit |
-
2008
- 2008-09-18 EP EP08164605A patent/EP2166006A1/en not_active Withdrawn
-
2009
- 2009-09-18 US US13/063,105 patent/US8624036B2/en active Active
- 2009-09-18 PL PL09783167T patent/PL2346841T3/pl unknown
- 2009-09-18 DK DK09783167.1T patent/DK2346841T3/en active
- 2009-09-18 WO PCT/EP2009/062109 patent/WO2010031835A2/en not_active Ceased
- 2009-09-18 CN CN200980136860.5A patent/CN102159558B/zh active Active
- 2009-09-18 PT PT97831671T patent/PT2346841E/pt unknown
- 2009-09-18 HR HRP20150395TT patent/HRP20150395T1/hr unknown
- 2009-09-18 AU AU2009294558A patent/AU2009294558B2/en active Active
- 2009-09-18 RU RU2011114992/04A patent/RU2520212C2/ru active
- 2009-09-18 SI SI200931170T patent/SI2346841T1/sl unknown
- 2009-09-18 ES ES09783167.1T patent/ES2534634T3/es active Active
- 2009-09-18 CA CA2737099A patent/CA2737099C/en active Active
- 2009-09-18 JP JP2011527334A patent/JP5571669B2/ja active Active
- 2009-09-18 EP EP09783167.1A patent/EP2346841B1/en active Active
-
2011
- 2011-03-10 IL IL211683A patent/IL211683A/en active IP Right Grant
-
2015
- 2015-04-08 CY CY20151100336T patent/CY1116176T1/el unknown
- 2015-04-22 SM SM201500098T patent/SMT201500098B/xx unknown
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